
==== Front
Aging Clin Exp Res
Aging Clin Exp Res
Aging Clinical and Experimental Research
1594-0667
1720-8319
Springer International Publishing Cham

39212862
2830
10.1007/s40520-024-02830-7
Research
Involvement of cognitive abilities in the occurrence of fractures in fallers aged 55 years or older: a cross-sectional study
Attoh-Mensah Elpidio kouakou.attoh-mensah@unilim.fr

16
Pothier Kristell 2
Loggia Gilles 13
Morello Remy 4
Chavoix Chantal 1
Marcelli Christian 15
1 grid.417831.8 0000 0004 0640 679X Normandie Univ, UNICAEN, INSERM, COMETE, CYCERON, Caen, 14000 France
2 https://ror.org/02wwzvj46 grid.12366.30 0000 0001 2182 6141 Department of Psychology, PAVeA Laboratory (UR 2114), University of Tours, Tours, 37000 France
3 https://ror.org/01k40cz91 grid.460771.3 0000 0004 1785 9671 Department of Geriatrics, Normandie Univ, UNICAEN, CHU de Caen, Caen, 14000 France
4 https://ror.org/01k40cz91 grid.460771.3 0000 0004 1785 9671 Department of Statistics and Clinical Research, Normandie Univ, UNICAEN, CHU de Caen, Caen, 14000 France
5 https://ror.org/01k40cz91 grid.460771.3 0000 0004 1785 9671 Department of Rheumatology, Normandie Univ, CHU de Caen, Caen, 14000 France
6 https://ror.org/02cp04407 grid.9966.0 0000 0001 2165 4861 Permanent address: Univ. Limoges, HAVAE, 123 Avenue Albert Thomas, UR, 20217, F-87000 Limoges, Limoges France
30 8 2024
30 8 2024
2024
36 1 18024 6 2024
5 8 2024
© The Author(s) 2024
2024
https://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Background

Both bone fragility and poor cognitive functions are known to contribute to fracture occurrence, but it remains unclear whether their contribution is independent of each other and which cognitive dysfunctions are most involved. This study aimed to clarify the involvement of various cognitive abilities in fall-related fractures among community-dwelling fallers aged 55 and over, and to determine whether poor cognitive abilities is a risk factor independent of bone fragility.

Methods

In a cross-sectional study, we collected sociodemographic and medical data, including bone mineral density (BMD), and performed cognitive and mobility assessments in 189 individuals with a history of fall in the previous year.

Results

Fallers with a fracture had poorer cognitive and mobility performance than non-injured fallers. Multivariate regressions revealed that cognition, BMD and other risk factors were independently associated with fracture among all participants (OR = 1.04, 95% CI = 1.01–1.08, p = 0.034 for completion time on part A of the Trail Making Test [TMT-A], and OR = 0.53, 95% CI = 0.33–0.84, p < 0.001 for BMD), particularly in women (OR = 0.77, 95% CI = 0.60–0.98, p = 0.039 for backward digit span score, and OR = 0.43, 95% CI = 0.25–0.75, p = 0.001 for BMD).

Conclusion

Thus, poor cognition, especially poor processing speed and working memory, is associated with an increased risk of fracture in fallers, particularly in women, regardless of BMD or other fracture risk factors. Hence, an in-depth cognitive evaluation should enhance the detection of fallers at risk of fracture, particularly in the absence of signs of osteoporosis, and thus ensure the best possible prevention.

Supplementary Information

The online version contains supplementary material available at 10.1007/s40520-024-02830-7.

Keywords

Fracture risk factors
Fall-related fracture
Bone fragility
Cognition
Executive function
Ministère des Solidarités et de la Santé2011-A00534-37 issue-copyright-statement© Springer Nature Switzerland AG 2024
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pmcIntroduction

Fall-related fractures are a major public health issue in older adults due to the number of people affected and serious related consequences. Each year, more than 30% of people aged 65 or over fall at least once, with many of these falls resulting in serious injury, especially fractures (4% of falls) [1, 2]. The incidence of fall-related fractures mainly increases from 50 years of age, with a greater incidence in women than in men aged 50–59 years (80.5% vs. 40.5%, respectively) [3, 4]. This high occurrence in middle-aged and older adults leads to substantial clinical and economic burdens to society through an increase in the rate of hospitalization, admission to emergency care and mortality or harmful consequences for people’s psyche and social life [2]. Therefore, preventing falls and related fractures in older adults has become a worldwide priority [2].

Osteoporosis has been identified as one of the leading risk factors for fractures [5, 6]. This systemic skeletal disease characterized by low bone mass, as determined by bone mineral density (BMD) or microarchitectural deterioration of bone tissues that can be non-invasively assessed by trabecular bone score (TBS), leads to increased bone fragility and fracture risk. The global aging of the population has significantly increased osteoporotic fractures, particularly in Western societies, where the lifetime risk is particularly high (40–50% in men and 13–22% in women) [7, 8]. Notably, bone fragility inherent to osteoporosis is not the only significant risk factor for fractures, as an important proportion of such fractures often occur in people with a normal BMD [5, 9]. One could thus assume that non-osteoporotic risk factors significantly contribute to the occurrence of fall-related fractures. Henceforth, better knowledge and accurate management of these other risk factors are crucial to preventing fracture [9]. These other risk factors mainly include gait disorders, polymedication, comorbidities, alcohol consumption, and cognitive impairment [1, 2].

Cognitive impairment has recently received particular attention because of its well-known association with falls. Indeed, it is now clearly established that there is a close link between cognition and walking and that poor cognitive abilities is a risk factor for falls and fractures [10]. Nevitt and colleagues’ study [11] showed for the first time that poor performance on an executive task was associated with an increased risk of fall-related fractures over a one-year period. Several prospective studies with follow-up periods up to 8 years have further confirmed this involvement of cognition, especially that of global cognition and executive function, in fractures [12–15]. In a systematic review of osteoporotic fracture prediction models, only one of 68 studies considered cognitive impairment, and more precisely impairment in global efficiency, revealing it to be a risk factor [16]. In a recent study we examined cognitive and anthropometric profiles in older women with post-fall limb fractures. Principal component analysis (PCA) identified four profiles, including one with normal BMD and low-medium cognitive performance and another with low BMD and high cognitive performance [17]. However, further research is warranted to elucidate how cognition, bone fragility, and other risk factors interact to increase susceptibility to fractures.

The aim of this study was thus to determine whether poor cognitive abilities is a risk factor for fractures independent of bone fragility in community-dwelling fallers aged 55 years and older. The involvement of specific cognitive dysfunction, identified by the assessment of various cognitive domains, and other risk factors were also investigated.

Materials and methods

Participants

Community-dwelling older adults aged 55 and over from a clinical research program at Caen University Hospital (France) were included. The age of 55 years was chosen as osteoporosis-related fracture become increasingly common from that age, especially in women [18]; besides, it is also an age when some cognitive abilities begin to decline.

Participants experienced one or more falls, with or without fracture, in the year before the study. Fallers with fractures were those with upper or lower limb fractures admitted to the orthopedic and emergency departments. Fallers without fractures were mostly recruited at the same hospital by questioning patients in consultation waiting rooms. In particular, they were asked whether they had fallen in the previous 6 months, whether it required medical care and if it did not, whether they would agree to participate in a research study on falls. We chose to include one control (faller without fracture) for every two cases (faller with fracture), a ratio quite acceptable for case-controls studies [19] and supported by previous research [20, 21]. Both fallers with and without fractures were excluded if they had fallen ≤ 2 months or ≥ 6 months ago, were unable to walk for 15 m without help, had pathologies affecting balance, drank > 21 units (for men) or > 14 units (for women) of alcohol per week, had severe depression (Montgomery–Åsberg Depression Rating Scale (MADRS) score > 30) or impaired vision (corrected acuity < 6/10). The lower Normandy Ethics Committee approved the present study (no. 2011A00556-35; clinical trial registration number: NCT02292316__Registration Date November 13, 2014), and each participant provided written informed consent.

Outcome measurements

Soon after inclusion, participants in both groups underwent several examinations, all carried out on the same afternoon.

Bone mineral density (BMD)

BMD was measured at the total hip and femoral neck by DXA using a Hologic 4500 A device, and the lowest T score of the two measured sites was used in the results. Using the World Health Organization criteria, participants were then classified as having a normal BMD (T score ≥ -1.0), an osteopenic BMD (T score between − 1.0 and − 2.5), or an osteoporotic BMD (T score ≤ -2.5 SD).

Cognitive and gait measurements

Cognitive and gait evaluations were performed by trained neuropsychologists who were blinded to the participants’ medical records.

Global cognitive efficiency was assessed with the Mini Mental State Examination (MMSE) [22] and Montreal Cognitive Assessment (MoCA) [23], two brief 30-point tests, with the latter being more sensitive in detecting mild cognitive impairment.

Processing speed was evaluated with three tests: part A of the Trail Making Test (TMT-A) [24] in which the participants must connect numbers randomly displayed on an A4 sheet of paper in ascending order, a copy of the figure of Rey. [25], and the Zazzo’s cancellation task [26] which consists of crossing out 40 target stimuli among 280 distractors. The variables retained were the completion times for the three tests.

Memory was assessed as follows: verbal short-term memory using the forward digit span test [27], and visual long-term memory using the reproduction from memory test of the Rey figure 3 min after copying, which is based on a 36-point scoring system.

In addition, working memory was assessed by two well-known WAIS subtests, the backward digit span test and the letter-digit sequence test [27], where the scores are based on the longest series correctly recalled.

Several executive functions were evaluated. Mental flexibility was assessed with part B of the TMT (TMT-B) [24], in which the subject must alternately connect numbers and letters in ascending and alphabetical order, respectively. The difference between TMT-B and TMT-A completion times (“TMT B-A”) was used as a relatively pure indicator of executive control abilities [28]. Verbal fluency was measured with the Isaacs Set Test (IST) [29], which requires the production of as many words as possible in 4 semantic categories in a given time (15 s for each category); the variable measured is the number of correct items. To assess inhibition, we used the Stroop test [30], which consists of three successive tasks of 45 s each: word reading (W), color patch naming (C), and interference condition, which requires the participants to name the ink color and ignore the word (CW); the interference score that reflects inhibition abilities was calculated using the following formula: CW/[(W + C)/2], where CW, W, and C are the number of correct items in the corresponding task [31].

Finally, to assess planning abilities, we analyzed the strategies used by the subject when copying the complex Rey figure; the scores ranged from 1 to 4 (1 reflecting a perfect strategy).

Functional mobility was assessed using the timed up and go (TUG) test [32], which requires the participant to stand up from an armchair, walk 3 m, turn, walk back, and sit down, all at a comfortable pace. Two trials were given, and the best performance (shortest time) was recorded. The TUG test was not administered to fallers with lower limb fracture to avoid the subsequent effects of this fracture on gait.

Other outcomes

During the medical examination, a physician carefully collected information about drugs taken by participants via medical prescriptions, which was confirmed by a medication history interview. The physician also collected information on comorbidities (from the Kaplan–Feinstein scale: hypertension, cardiac, cerebral or psychic, respiratory, renal, hepatic, gastrointestinal, peripheral vascular, cancer, locomotor, alcoholism, and miscellaneous) [33], the number of previous falls experienced in the preceding twelve months, and risk factors for falls (hypotension, rheumatological disorders, tinnitus, muscular weakness, abnormal proprioceptive sensitivity in the lower limbs, and age ≥ 75 years). These risk factors were defined by consensus between physician-investigators after elimination of the exclusion criteria (e.g., low visual acuity, depression) and the factors used as variables of interest (BMD, cognition and mobility). Muscular strength was assessed with a handgrip dynamometer, which has been recognized as a good simple measure of muscle strength and correlates with leg strength [34]; each participant performed 2 trials per hand, and the best performance was recorded.

Statistical analysis

We compared sociodemographic characteristics and outcome measures based on fall severity and bone density using the following tests: Student’s t test, the Mann‒Whitney test, the chi‒squared test, the Kruskal‒Wallis test, and ANOVA with the Bonferroni post hoc correction applied using the sequential method after pairwise comparisons. The normality of data distribution was verified by the Shapiro‒Wilk test. Cognitive and mobility data included both continuous raw scores and categorical impaired scores (MoCA and IST < 25), impaired scores for MMSE and TMT-A and TMT-B completion times range from < 23 to < 26, <62.60 to < 39 s, and < 157.95 to < 123.51 s, respectively, depending on educational level in persons aged 50 years and over, [35, 36] and impaired scores for the TUG range from ≥ 9 s to ≥ 12.7 s, depending on age [37].

We performed logistic regressions to test the association between variables and fracture occurrence using the backward stepwise method. Both univariate and multivariate regressions were performed. Co-variables included in the multivariate analysis were those that scored a p-value < 10% in the univariate analysis. Variables with ceiling or floor effects or which overlap were excluded. We also conducted a PCA with varimax rotation to identify key outcome measures explaining fracture variance. The Kaiser‒Meyer‒Olkin (KMO) measure ensured sampling adequacy. Components with eigenvalues > 1 and variables with loadings > 0.50 were retained [38]. To reduce any potential bias resulting from an expected strong association between women and fractures, the above analyses were also conducted separately for men and women.

All analyses were performed with SPSS 24.0® software (IBM; Armonk, NY, USA), and the significance threshold was set at 0.05.

Results

Out of the 376 injured fallers that agreed to participate in the study, 250 did not meet the inclusion criteria, resulting in 126 injured fallers included in the present study. After searching for non-injured fallers with a ratio of one-control for two cases, 63 individuals were added which brings the total to 189 participants. Fallers with a lower limb fracture represented 40% of the injured fallers. As shown in Table 1, the mean age of the study population was 71 years, and the majority were women (83%). The mean BMD T-score (-1.71 ± 3.75; -1.71 ± 1.02 for women and − 1.73 ± 0.86 for men) was within the osteopenic range. Global cognitive efficiency and mobility scores were within normal ranges (i.e., 27, 26 and 9.5 s for the MMSE, MoCA and TUG, respectively).

Table 1 Characteristics of the study population and comparisons between fall severity (with or without fracture) and bone density status

	ALL
N=189	Fall- severity	Bone density status	
Non-injured
(n=63)	With fracture
(n=126)	p-value	Normal BMD
(n=73)	Osteopenia
(n=78)	Osteoporosis
(n=38)	p-value	
General characteristics	
Age, years	71.05 ± 9.23	71.03 ± 9.71	71.08 ± 8.27	0.973a	67.55 ± 6.81	71.12 ± 10.23$	76.71 ± 8.64 *, #	0.001 e	
Education, years	11.34 ± 3.48	13.62 ± 4.57	11.97 ± 5.40	0.001 b	12.38 ± 4.07	12.21 ± 4.34	11.37 ± 3.31	0.653d	
Women, number (%)	156(83)	38(63)	118(94)	0.001 c	61(83)	60(38)	33(88)	0.724c	
Handgrip strength, kg	21.09 ± 7.93	24.70 ± 9.22	19.27 ± 6.52	0.001 a	21.95 ± 8.14	21.64 ± 8.20	18.60 ± 6.90	0.254e	
BMI, kg/m2	27.33 ± 7.05	26.86 ± 5.15	29.95 ± 6.71	0.545b	29.32 ± 5.22	26.43 ± 4.56$	23.91 ± 4.16 *,#	0.001 d	
Comorbidities, number	1.76 ± 1.42	1.97 ± 1.53	1.66 ± 1.36	0.213b	1.79 ± 1.44	1.53 ± 1.50	2.0 ± 1.13	0.232e	
Risk factors for falls, number	0.94 ± 0.95	0.78 ± 0.62	1.02 ± 0.98	0.076a	0.63 ± 0.48	0.95 ± 0.89$	1.45 ± 1.05 *,#	0.001 e	
Falls in past 12 months, number	1.85 ± 0.18	1.75 ± 0.20	1.89 ± 0.24	0.702a	1.95 ± 0.34	1.77 ± 0.25	1.84 ± 0.34	0.908a	
Prescribed drugs, number	4.13 ± 3.75	5.30 ± 3.63	5.46 ± 4.13	0.786c	5.04 ± 3.58	5.20 ± 3.87	6.52 ± 4.78	0.153e	
Post-fall and bone density status	
Fall-related fractures, number (%)	126(67)	0	100	NA	41(56)	47(60)	34(89) *, #	0.002 c	
BMD, T-score	-1.71 ± 3.75	-1.44 ± 0.89	-1.86 ± 1.02	0.007 a	-1.01 ± 0.77	-1.71 ± 0.51$	-3.08 ± 0.57 *, #	0.0001 e	
Global cognition	
MMSE score	27.59 ± 2.81	28.30 ± 1.69	27.73 ± 3.18	0.028 b	28.25 ± 1.92	27.82 ± 2.03	25.84 ± 4.57*	0.004 d	
Impaired MMSE, number (%)	18(10)	5(8)	13(10)	0.046 c	4(5)	7(9)	7(18)	0.076c	
MoCA score	26.01 ± 4.04	27.97 ± 2.52	25.91 ± 4.16	0.001 b	26.86 ± 3.50	26.48 ± 3.18	24.00 ± 5.46*	0.005 d	
Impaired MoCA, number (%)	48(26)	6(10)	42(33)	0.002 c	13(18)	18(23)	17(45) *	0.035 c	
Processing speed	
TMT A score (sec)	40.08 ± 19.51	34.92 ± 11.02	42.73 ± 22.25	0.041 b	35.51 ± 12.9	38.47 ± 15.7	51.95 ± 30.8 *, #	0.001 d	
Impaired TMT A, number (%)	37(20)	9(14)	28(23)	0.118c	13(18)	14(19)	10(27)	0.527c	
Zazzo, completion time (sec)	136.30 ± 47.7	126.5 ± 35.7	141.3 ± 52.3	0.135b	123.5 ± 37.3	131.0 ± 40.0	170.80 ± 65.0 *, #	0.001 d	
Rey Figure, copy time (sec)	178.1 ± 90.8	156.1 ± 84.11	200.6 ± 29.4	0.004 a	168.2 ± 86.2	170.8 ± 76.7	245.9 ± 99.6 *, #	0.006 d	
Memory	
Forward digit span (score)	7.73 ± 1.94	8.16 ± 1.87	7.52 ± 1.95	0.033 a	8.0 ± 1.92	7.88 ± 2.0	7.11 ± 1.85	0.065e	
Backward digit span (score)	5.30 ± 1.52	5.70 ± 1.73	4.91 ± 1.75	0.004 a	5.45 ± 2.04	5.32 ± 1.62	4.43 ± 1.36*, #	0.013 e	
Letter digit sequence (score)	8.67 ± 2.85	9.24 ± 2.96	8.36 ± 2.75	0.042 a	8.99 ± 2.61	9.10 ± 3.04	7.44 ± 2.57*, #	0.029 e	
Rey Figure, recall (score)	16.30 ± 4.77	15.54 ± 5.78	15.98 ± 5.22	0.135b	15.82 ± 5.68	14.60 ± 6.10	13.62 ± 5.94	0.132d	
Flexibility and Fluency	
TMT-B completion time (sec)	97.66 ± 61.80	83.29 ± 35.75	105.29 ± 70.9	0.027 b	86.37 ± 47.55	95.85 ± 49.71	123.14 ± 97.44*	0.077d	
Impaired TMT-B, number (%)	31(16)	8(13)	23(20)	0.175c	12(17)	17(22) $	2(4)	0.039 c	
TMT B-A score (sec)	59.66 ± 51.08	49.24 ± 30.70	65.19 ± 58.51	0.047 b	51.40 ± 40.19	57.90 ± 39.51	78.28 ± 81.23*	0.028 d	
Impaired TMT B-A, number (%)	22(12)	5(8)	17(15)	0.153c	7(10)	8(12)	7(17)	0.095c	
Isaacs Set test (IST) score	36.22 ± 7.42	38.19 ± 7.15	35.22 ± 7.38	0.009 a	38.04 ± 7.18	36.61 ± 6.55	32.30 ± 8.22*, #	0.001 e	
Impaired IST, number (%)	43(23)	11 (18)	32(26)	0.136c	18(25)	15(19)	10(26)	0.625c	
Inhibition	
Stroop (score)	0.48 ± 0.10	0.47 ± 0.08	0.51 ± 0.14	0.055a	0.50 ± 0.11	0.47 ± 0.10	0.49 ± 0.09	0.077e	
Planning abilities	
Rey Figure, copying strategy (score)	2.32 ± 1.15	2.16 ± 1.24	2.48 ± 1.32	0.042 a	2.47 ± 1.35	2.24 ± 1.27	2.51 ± 1.30	0.490d	
Functional mobility	
TUG€ (sec)	9.50 ± 3.48	8.63 ± 1.92	10.24 ± 4.29	0.005 a	9.11 ± 2.54	8.75 ± 1.95	12.64 ± 6.74*,#	0.001 e	
Impaired TUG, number (%)	44(24)	17(27)	27(37)	0.001 c	24(33)	13(16) $	7(18)	0.001 c	
Unless indicated, values are mean ± SD; aStudent’s t-test, bU test of Mann-Whitney, cChi-square test, dKruskall-Walis or eOne-way ANOVA. BMI: Body Mass Index; BMD: Bone Mineral Density; MMSE: Mini Mental State Examination; MoCA: Montreal Cognitive Assessment; IST: Isaacs Set Test; TUG: Time Up and Go; TMT: Trail Making Test. Impaired scores for MoCA and Isaacs Set test are < 25. Impaired scores for the MMSE, TMT-A and TMT-B completion time range from <23 to <26, <62.60 to <39 s, and <157.95 to <123.51 s, respectively, depending on educational level in persons aged 50 years and over. Impaired scores for the TUG range from ≥9 s to ≥12.7 s, depending on age. Significant post-hoc intergroup differences are represented by the following symbols: $ for or “osteopenia vs. normal BMD”, * for “osteoporosis vs. normal”, and # for “osteoporosis vs. osteopenia”; the p-values of the post-hoc analyses are specified in the text. €n=123 participants only because not tested in fallers with lower limb fracture so as to avoid this fracture’s after effects on gait

Intergroup comparisons revealed that fallers with fractures were significantly less educated, more often women, and had lower handgrip strength and T scores than non-injured fallers (p ≈ 0.001 each). They also had poorer scores in global cognition (MMSE p = 0.028, MoCA p = 0.001), processing speed (TMT-A p = 0.041, Rey Figure-copy time p = 0.004), memory (p = 0.037, 0.004 and 0.044 for the forward and backward digit span, and the letter digit sequence, respectively), mobility (TUG p = 0.005) and others (see Table 1). Additionally, they had greater proportions of impaired MMSE, MoCA, and TUG scores than did the non-injured group (p = 0.042, 0.002, 0.001, respectively).

Significant differences in general characteristics and cognitive and mobility scores were found when comparing participants by bone density status (Table 1). Bonferroni post hoc analyses showed that, compared to both the normal BMD and osteopenia groups, those with osteoporosis were older (p = 0.001, 0.005), had a lower BMI (p = 0.001, 0.027), had more fall risk factors (p = 0.001, 0.019), and had a greater proportion of fall-related fractures. The participants also had poorer scores for global cognition (MMSE: p = 0.001, 0.028; MoCA: p = 0.001, 0.002), processing speed (TMT A: p = 0.003, 0.025; Rey Figure-copy time: p = 0.001, 0.011; Zazzo completion time: p = 0.001, 0.002), working memory (backward digit span: p = 0.001, 0.002; letter digit sequence: p = 0.029, 0.017), flexibility, fluency (TMT B-A vs. normal BMD: p = 0.039; Isaacs Set Test: p = 0.003, 0.045), and mobility (TUG: p = 0.015, 0.003). The osteoporosis group had more impaired MoCA scores than did the normal BMD group (p = 0.025). Additionally, the osteopenia group was older (p = 0.041) and had a lower BMI (p = 0.001), more fall risk factors (p = 0.043), and more impaired performance on the TMT-B (p = 0.038) and TUG (p = 0.011) tests than the normal BMD group.

The following variables, which showed ceiling or floor effects in their distribution or were considered overlapping variables, were then excluded from the regression analysis: MMSE, MoCA, Rey Figure (copy time, recall and strategy), forward digit span, TMT-B completion time, and TUG. As shown in Table 2, the results of the multivariate regression computed across all participants revealed an independent association between the presence of fracture and the following variables: age (OR = 0.93, 95% CI = 0.88–0.98, p = 0.010), education (OR = 0.87, 95% CI = 0.79–0.97, p = 0.013), BMD (OR = 0.49, 95% CI = 0.30–0.81, p = 0.015), percentage of women (OR = 8.42, 95% CI = 3.15–22.51, p = 0.00002), and TMT-A score (OR = 1.03, 95% CI = 1.01–1.08, p = 0.034).

Table 2 Results from the logistic regressions performed to analyze the relationships between fall severity (absence vs. presence of fracture) and variables across all participants

	Univariate	Multivariate	
OR	95% CI	p-value	OR	95% CI	p-value	
Age	0.97	0.93-1.02	0.079	0.93	0.88-0.98	0.013	
Education	0.89	0.80-0.90	0.042	0.87	0.79-0.97	0.013	
Percentage of women	9.70	4.04-23.30	0.0001	8.42	3.15-22.51	0.00002	
BMI	1.04	0.96-1.13	0.286				
BMD	0.54	0.36-0.81	0.003	0.47	0.29-0.75	0.001	
Handgrip strength	0.97	0.92-1.03	0.359				
Zazzo completion time	0.99	0.97-1.01	0.293				
TMT-A completion time	1.03	1.01-1.05	0.010	1.03	1.01-1.08	0.034	
TMT B-A	1.03	0.98-1.04	0.706				
IST score	0.99	0.91-1.07	0.804				
Backward digit span score	0.86	0.74-0.99	0.040				
Letter digit sequence score	0.91	0.74-1.11	0.372				
Stroop Score	0.11	0.01-14.79	0.387				
Risk factors for falls, number	1.15	0.73-1.82	0.539				
Comorbidities, number	0.96	0.72-1.28	0.814				
Prescribed drugs, number	1.13	0.47-2.68	0.775				
BMI: Body Mass Index; BMD: Bone Mineral Density; TMT: Trail Making Test; IST: Isaacs Set Test

Regarding the sex-specific analyses, as displayed in Table 3, the logistic regressions conducted in women showed that the presence of fracture was independently associated with age (OR = 0.90, 95% CI = 0.84–0.95, p = 0.001), BMD (OR = 0.43, 95% CI = 0.25–0.75, p = 0.001), backward digit span score (OR = 0.77, 95% CI = 0.60–0.98, p = 0.039), and TMT-A score (OR = 1.05, 95% CI = 1.01–1.10, p = 0.017). In male participants, logistic regressions did not reveal any associations between the presence of a fall-related fracture and the variables of interest (data not shown).

Table 3 Results from the logistic regressions performed to analyze the relationships between fall severity (absence vs. presence of fracture) and variables in women

	Univariate	Multivariate	
	OR	95% CI	p-value	OR	95% CI	p-value	
Age	0.99	0.95-1.03	0.087	0.90	0.84-0.95	0.001	
Education	0.88	0.79-0.97	0.015				
BMI	0.98	0.92-1.05	0.729				
BMD	0.55	0.37-0.82	0.003	0.43	0.25-0.75	0.003	
Handgrip strength	0.97	0.90-1.03	0.336				
Zazzo completion time	1.01	0.97-1.02	0.186				
TMT-A completion time	1.03	1.01-1.07	0.022	1.05	1.01-1.10	0.017	
TMT B-A	1.01	0.99-1.02	0.069				
IST score	0.92	0.88-0.97	0.006				
Backward digit span score	0.75	0.61-0.93	0.010	0.77	0.60-0.98	0.039	
Letter digit sequence score	0.86	0.75-1.00	0.051				
Stroop Score	0.04	0.01-2.63	0.135				
Risk factors for fall, number	1.09	0.74-1.60	0.639				
Comorbidities, number	0.87	0.75-1.27	0.876				
Prescribed drugs, number	1.07	0.51-2.24	0.850				
BMI: Body Mass Index; BMD: Bone Mineral Density; TMT: Trail Making Test; IST: Isaacs Set Test

The results from the PCA across all 189 participants are shown in Table 4. The KMO measure (0.749) indicated that the sample size was adequate. We identified four components, C1 to C4, with eigenvalues > 1; these four components explained 67% of the total variance. The distribution of the variables within the components was as follows: C1 (age, Zazzo and TMT-A completion times, TMT B-A, and risk factor for falls), C2 (education, backward digit span and letter digit sequence scores), C3 (percentage of women and handgrip strength) and C4 (BMD, BMI). The results of the PCA performed for women (KMO = 0.796) are shown in Table 5. Three independent components, C1w to C3w, explained 54% of the variance. The variable distribution was very similar to that across all participants, although it was grouped into only 3 components, with the first one including more cognitive variables than in all participants: C1w (Zazzo and TMT-A completion times, TMT B-A, IST, Stroop, backward digit span and letter digit sequence scores, and education), C2w (age, handgrip strength, and risk factors for falls), and C3w (BMD, BMI, and number of comorbidities).

Table 4 Components matrix after varimax rotation, across all participants

	Components	
	C1	C2	C3	C4	
Age	0.746				
Zazzo completion time	0.715				
TMT-A completion time	0.614				
TMT B-A	0.578				
Risk factors for falls, number	0.633				
BMI				0.866	
BMD				0.741	
Women (%)			0.900		
Handgrip strength (Kg)			0.851		
Backward digit span score		0.833			
Letter digit sequence score		0.772			
Education (years)		0.675			
Eigenvalues	4.571	2.106	1.712	1.250	
Total variance (%)	28.57	13.16	10.70	7.81	
BMI: Body Mass Index; BMD: Bone Mineral Density; TMT: Trail Making Test

Table 5 Components matrix after varimax rotation in women

	Components	
	C1w	C2 w	C3 w	
Zazzo completion time	-0.609			
TMT-A completion time	-0.703			
TMT B-A	-0.635			
IST score	0.740			
Stroop score	0.534			
Backward digit span score	0.657			
Education (years)	0.532			
Letter digit sequence score	0.760			
BMI			0.638	
BMD			0.820	
Age		0.774		
Handgrip strength (Kg)		-0.694		
Risk factors for falls, number		0.709		
Comorbidities, number			0.638	
Eigenvalues	4.676	2.098	1.392	
Total variance (%)	31.17	13.98	9.20	
BMI: Body Mass Index; BMD: Bone Mineral Density; TMT: Trail Making Test; IST: Isaacs Set Test

Due to the lack of significant findings from the logistic regression in men, PCA was not performed for this subgroup.

Discussion

This is the first study to our knowledge to compare the involvement of cognitive abilities and bone density in fractures among community-dwelling fallers aged 55 years and older. Our findings indicate poorer cognitive performance in fractured participants than in non-injured fallers and also among osteoporotic fallers than in those with osteopenia and normal BMD. Logistic regression analysis indicated that poor cognitive abilities, particularly processing speed and working memory, were independent of BMD and other fracture risk factors in fallers with fractures, predominantly among women.

There were numerous differences when considering fall severity, as well as between participants with and without osteoporosis. In agreement with the literature, fallers who experienced a fracture were mainly women [3], had poorer muscle strength and were less educated than non-injured fallers. Furthermore, the osteoporotic group had a lower BMI and more risk factors for falls than the other two groups, as also reported before [3]. Interestingly, we also found that fallers who experienced a fracture and those with osteoporosis had poorer cognitive and mobility performance than non-injured fallers and those with normal BMD or osteopenia, respectively. This could suggest a link between osteoporosis, fracture and cognitive abilities. The logistic regression and PCA analyses further specify the nature of this link.

The poor cognitive abilities of fallers who experienced a fracture is in line with previous data that have clearly established a strong link between cognition, falls and fractures in both cross-sectional and prospective studies, with a high risk of fracture in people with poor cognition [11–15, 17]. While our study confirmed the involvement of poor cognitive abilities in fractured fallers, it revealed the most influential cognitive functions, which could not be identified in previous studies that focused mainly on global cognition and sometimes executive function. Our comprehensive cognitive assessment revealed significantly lower performance in processing speed, memory (particularly working memory), mental flexibility, verbal fluency, and planning among fractured versus non-injured fallers, with inhibition showing a trend toward significance. Notably, most participants showed cognitive performance within the normal range. Only 10 and 8% of the injured and non-injured fallers, respectively, had impaired MMSE scores, and the mean scores were relatively high (21.35 and 23.5, respectively). This suggests that the risk of fracture may manifest as soon as cognitive performance becomes nonoptimal.

The cross-sectional association between fractures in fallers and poor cognitive abilities, irrespective of BMD, is a novel finding. Multivariate regression revealed that poor processing speed was the main cognitive variable linked to fractures in fallers, independent of BMD. As individuals age, processing speed diminishes, impacting various cognitive domains and increasing fracture risk regardless of bone fragility. Notably, most people who fracture after a fall have a normal BMD [5, 9, 39]. In addition, this distinct involvement of cognitive abilities and osteoporosis in fracture occurrence is in line with our recent study, which identified different profiles in older women who experienced a fracture of the upper or lower limb following a fall [17]. Indeed, among the 4 identified profiles, two were clearly opposed in terms of osteoporosis and cognitive performance: the profile with the most osteoporotic participants (30%) had the best cognitive performance, whereas one of the two profiles with no osteoporotic participants displayed the lowest cognitive performance. It could thus be assumed that in the case of normal BMD, poor cognition could have significantly contributed to the fracture, at least in some of them.

Interestingly, the low cognitive performance in case of fracture occurrence in fallers was replicated in the gender-specific analyses performed among women, highlighting the involvement of processing speed and working memory. This finding is all the more relevant as the PCA in women identified TMT-A and backward digit span in the variables of the C1w component, which explained the most variance (31%). The fact that the involvement of cognition in fracture was identified for working memory but not for executive functions might seem odd at first sight. Indeed, few studies have identified the contribution of poor executive functioning to fracture occurrence [11, 14, 15]. Nevertheless, it is well known that poor performance in attention, executive function, and working memory are associated with gait instability and that these cognitive disorders are predictive of falls [10]. Furthermore, reports have indicated that working memory demand affects accurate reactions following a loss of balance, especially in fallers [40]. In addition, working memory is classically recognized as being at the interface between memory, attention, and executive functions, and it is often considered that the central executive component of working memory is an executive function and that executive function includes working memory [41–43].

The absence of the polypharmacy variable in the 4 PCA profiles identified may seem surprising. It is well-established that polypharmacy, particularly involving psychotropic or anticholinergic drugs, significantly contributes to fracture occurrence. Since these drugs are also known to impact both cognitive abilities and mobility [44–46], future studies should investigate whether their contribution to fracture risk is mediated by their effects on cognitive functions.

Some limitations can be addressed. First, one could argue that the present findings may not be relevant to the general population since the participants were exclusively fallers. Nevertheless, as previously discussed in detail [45], our population is very similar to the general population, as the mean cognitive and mobility scores fall within the normal ranges. In addition, because 30% of individuals older than 65 years fall every year [2] and since we specifically searched for individuals who had fallen in the previous year, after our 5 years of inclusion, we likely collected a significant part of the general population. Second, significant relationships between the presence of a fall-related fracture and poor performance of specific cognitive functions in women were not found in men. Nevertheless, we found similar results across all participants and among women. In addition, given the absence of notable discrepancies between men and women across all variables of interest (see supplementary Table S1), it is likely that the absence of a relationship between fracture and cognition might result from the relatively small sample of men. The fact that only 20% of men were recruited could be explained by various factors, such as the higher prevalence of osteoporosis in women than in men with advancing age and the lower participation rate of men in research investigations addressing this topic [15, 17]. However, further studies are required to test this relationship in a larger sample of men. Assessment of bone microarchitecture, using TBS for instance, could also have provided interesting complementary information to BMD. However, it has been shown in population-based studies that TBS has the same discriminatory value, and no additive value, for fracture discrimination as compared to BMD alone [47]. Furthermore, the absence of a follow-up study confirming the relationships between specific cognitive abilities and fracture occurrence in a longitudinal setting could also be a limitation. However, the cross-sectional association revealed in this study aligns with the increasing body of evidence highlighting the influence of cognition on the occurrence of fractures in fallers.

Conclusion

This study highlights the involvement of poor cognitive abilities in fractures among community-dwelling fallers aged 55 and over. Cognitive impairments were greater in fallers with fractures and in participants with osteoporosis than in those with osteopenia or normal BMD. Notably, poor cognitive abilities, particularly processing speed and working memory, in case of fracture occurrence was independent of bone fragility, especially in women. These findings underscore the importance of assessing cognitive abilities in managing fractures. Recent recommendations have urged the inclusion of routine cognitive assessments in multifactorial fracture risk assessments in older adults [2]. We recommend extending cognitive assessments to younger fallers (aged 55 years), especially those with osteoporosis, comorbidities, and other common fracture risk factors. This will ensure the best possible prevention.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary Material 1

Acknowledgements

The authors thank Drs. Valérie Caridroit, Thiphaine Ciappucini, Murielle Michel, Pascale Lescure, and Pablo Descatoire for their participation in the medical examinations; the neuropsychologists Marion Hommet and Marion Delarue for the cognitive assessment; and Anita Jamet for her contribution to the recruitment of participants.

Author contributions

E.A.-M. and C.C. wrote the main manuscript text.E.A.-M. and R.M. performed the analyses, and E.A.-M. prepared the tables. C.M. and C.C. designed the study. K.P., E.A.-M., G.L., C.C. and C.M., conducted the experiments. C.M. secured the funding.

Funding

This work was supported by the French Ministry of Health (PHRC Programme Hospitalier de Recherche Clinique 2011 no. 2011-A00534-37).

Data availability

The data that support the findings of this study are available on request to the corresponding author. The data are not publicly available due to privacy or ethical restrictions.

Declarations

Ethics approval and consent to participate

The lower Normandy Ethics Committee approved the present study (no. 2011A00556-35; clinical trial registration number: NCT02292316), and each participant provided written informed consent.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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References

1. Yeung SSY Reijnierse EM Pham VK Trappenburg MC Lim WK Meskers CGM Sarcopenia and its association with falls and fractures in older adults: a systematic review and meta-analysis J Cachexia Sarcopenia Muscle 2019 10 485 500 10.1002/jcsm.12411 30993881
Yeung SSY, Reijnierse EM, Pham VK, Trappenburg MC, Lim WK, Meskers CGM et al (2019) Sarcopenia and its association with falls and fractures in older adults: a systematic review and meta-analysis. J Cachexia Sarcopenia Muscle 10:485–50030993881 10.1002/jcsm.12411
2. Montero-Odasso M van der Velde N Martin FC Petrovic M Tan MP Ryg J World guidelines for falls prevention and management for older adults: a global initiative Age Ageing 2022 51 afac205 10.1093/ageing/afac205 36178003
Montero-Odasso M, van der Velde N, Martin FC, Petrovic M, Tan MP, Ryg J et al (2022) World guidelines for falls prevention and management for older adults: a global initiative. Age Ageing 51:afac20536178003 10.1093/ageing/afac205
3. Court-Brown CM Duckworth AD Clement ND McQueen MM Fractures in older adults. A view of the future? Injury 2018 49 2161 2166 10.1016/j.injury.2018.11.009 30526922
Court-Brown CM, Duckworth AD, Clement ND, McQueen MM (2018) Fractures in older adults. A view of the future? Injury 49:2161–216630526922 10.1016/j.injury.2018.11.009
4. Toth E Banefelt J Åkesson K Spångeus A Ortsäter G Libanati C History of previous fracture and imminent fracture risk in Swedish Women aged 55 to 90 years presenting with a fragility fracture J Bone Min Res 2020 35 861 868 10.1002/jbmr.3953
Toth E, Banefelt J, Åkesson K, Spångeus A, Ortsäter G, Libanati C (2020) History of previous fracture and imminent fracture risk in Swedish Women aged 55 to 90 years presenting with a fragility fracture. J Bone Min Res 35:861–86810.1002/jbmr.3953
5. Ja K, C C, Jy RR R (2019) European guidance for the diagnosis and management of osteoporosis in postmenopausal women. Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. 10.1007/s00198-018-4704-5
6. Curran D Maravic M Kiefer P Tochon V Fardellone P Epidemiology of osteoporosis-related fractures in France: a literature review Joint Bone Spine 2010 77 546 551 10.1016/j.jbspin.2010.02.006 20378383
Curran D, Maravic M, Kiefer P, Tochon V, Fardellone P (2010) Epidemiology of osteoporosis-related fractures in France: a literature review. Joint Bone Spine 77:546–55120378383 10.1016/j.jbspin.2010.02.006
7. Dargent-Molina P Bréart G [Epidemiology of falls and fall-related injuries in the aged] Rev Epidemiol Sante Publique 1995 43 72 83 7892520
Dargent-Molina P, Bréart G (1995) [Epidemiology of falls and fall-related injuries in the aged]. Rev Epidemiol Sante Publique 43:72–837892520
8. Johnell O Kanis JA An estimate of the worldwide prevalence and disability associated with osteoporotic fractures Osteoporos Int 2006 17 1726 1733 10.1007/s00198-006-0172-4 16983459
Johnell O, Kanis JA (2006) An estimate of the worldwide prevalence and disability associated with osteoporotic fractures. Osteoporos Int 17:1726–173316983459 10.1007/s00198-006-0172-4
9. Siris ES Brenneman SK Miller PD Barrett-Connor E Chen Y-T Sherwood LM Predictive value of low BMD for 1-year fracture outcomes is similar for postmenopausal women ages 50–64 and 65 and older: results from the National osteoporosis Risk Assessment (NORA) J Bone Min Res 2004 19 1215 1220 10.1359/JBMR.040508
Siris ES, Brenneman SK, Miller PD, Barrett-Connor E, Chen Y-T, Sherwood LM et al (2004) Predictive value of low BMD for 1-year fracture outcomes is similar for postmenopausal women ages 50–64 and 65 and older: results from the National osteoporosis Risk Assessment (NORA). J Bone Min Res 19:1215–122010.1359/JBMR.040508
10. Montero-Odasso M Verghese J Beauchet O Hausdorff JM Gait and cognition: a complementary approach to understanding brain function and the risk of falling J Am Geriatr Soc 2012 60 2127 2136 10.1111/j.1532-5415.2012.04209.x 23110433
Montero-Odasso M, Verghese J, Beauchet O, Hausdorff JM (2012) Gait and cognition: a complementary approach to understanding brain function and the risk of falling. J Am Geriatr Soc 60:2127–213623110433 10.1111/j.1532-5415.2012.04209.x
11. Nevitt MC Cummings SR Hudes ES Risk factors for injurious falls: a prospective study J Gerontol 1991 46 M164 170 10.1093/geronj/46.5.M164 1890282
Nevitt MC, Cummings SR, Hudes ES (1991) Risk factors for injurious falls: a prospective study. J Gerontol 46:M164–1701890282 10.1093/geronj/46.5.M164
12. Alfaro-Acha A Ostir GV Markides KS Ottenbacher KJ Cognitive status, body mass index, and hip fracture in older hispanic adults J Am Geriatr Soc 2006 54 1251 1255 10.1111/j.1532-5415.2006.00820.x 16913994
Alfaro-Acha A, Ostir GV, Markides KS, Ottenbacher KJ (2006) Cognitive status, body mass index, and hip fracture in older hispanic adults. J Am Geriatr Soc 54:1251–125516913994 10.1111/j.1532-5415.2006.00820.x
13. Bergland A Wyller TB Risk factors for serious fall related injury in elderly women living at home Inj Prev 2004 10 308 313 10.1136/ip.2003.004721 15470013
Bergland A, Wyller TB (2004) Risk factors for serious fall related injury in elderly women living at home. Inj Prev 10:308–31315470013 10.1136/ip.2003.004721
14. Cauley JA Cawthon PM Peters KE Cummings SR Ensrud KE Bauer DC Risk factors for hip fracture in older men: the osteoporotic fractures in men Study (MrOS) J Bone Min Res 2016 31 1810 1819 10.1002/jbmr.2836
Cauley JA, Cawthon PM, Peters KE, Cummings SR, Ensrud KE, Bauer DC et al (2016) Risk factors for hip fracture in older men: the osteoporotic fractures in men Study (MrOS). J Bone Min Res 31:1810–181910.1002/jbmr.2836
15. Smith C Seematter-Bagnoud L Santos-Eggimann B Krief H Bula CJ Executive function and prospective falls: a 6-year longitudinal study in community-dwelling older adults BMC Geriatr 2023 23 140 10.1186/s12877-023-03790-9 36899323
Smith C, Seematter-Bagnoud L, Santos-Eggimann B, Krief H, Bula CJ (2023) Executive function and prospective falls: a 6-year longitudinal study in community-dwelling older adults. BMC Geriatr 23:14036899323 10.1186/s12877-023-03790-9
16. Sun X Chen Y Gao Y Zhang Z Qin L Song J Prediction models for osteoporotic fractures risk: a systematic review and critical Appraisal Aging Disease 2022 13 1215 1238 10.14336/AD.2021.1206 35855348
Sun X, Chen Y, Gao Y, Zhang Z, Qin L, Song J et al (2022) Prediction models for osteoporotic fractures risk: a systematic review and critical Appraisal. Aging Disease 13:1215–123835855348 10.14336/AD.2021.1206
17. Baillet M Morello R Vittecoq O Chavoix C Marcelli C Bone, cognitive, and anthropometric profiles and their relation to fracture sites in fallers: a cross-sectional study Osteoporos Int 2023 34 901 913 10.1007/s00198-023-06701-1 36959306
Baillet M, Morello R, Vittecoq O, Chavoix C, Marcelli C (2023) Bone, cognitive, and anthropometric profiles and their relation to fracture sites in fallers: a cross-sectional study. Osteoporos Int 34:901–91336959306 10.1007/s00198-023-06701-1
18. Compston JE McClung MR Leslie WD Osteoporos Lancet 2019 393 364 376 10.1016/S0140-6736(18)32112-3
Compston JE, McClung MR, Leslie WD (2019) Osteoporos Lancet 393:364–37610.1016/S0140-6736(18)32112-3
19. Rothman KJ, Rothman KJ (2012) Epidemiology: An Introduction, Second Edition, Second Edition. Oxford University Press: Oxford, New York
20. Khedher L Bonny J-M Marques A Durand E Pereira B Chupin M Intrasubject subcortical quantitative referencing to boost MRI sensitivity to Parkinson’s disease Neuroimage Clin 2022 36 103231 10.1016/j.nicl.2022.103231 36279753
Khedher L, Bonny J-M, Marques A, Durand E, Pereira B, Chupin M et al (2022) Intrasubject subcortical quantitative referencing to boost MRI sensitivity to Parkinson’s disease. Neuroimage Clin 36:10323136279753 10.1016/j.nicl.2022.103231
21. Marques A Macias E Pereira B Durand E Chassain C Vidal T Volumetric changes and clinical trajectories in Parkinson’s disease: a prospective multicentric study J Neurol 2023 270 6033 6043 10.1007/s00415-023-11947-0 37648911
Marques A, Macias E, Pereira B, Durand E, Chassain C, Vidal T et al (2023) Volumetric changes and clinical trajectories in Parkinson’s disease: a prospective multicentric study. J Neurol 270:6033–604337648911 10.1007/s00415-023-11947-0
22. Folstein MF Folstein SE McHugh PR Mini-mental state. A practical method for grading the cognitive state of patients for the clinician J Psychiatr Res 1975 12 189 198 10.1016/0022-3956(75)90026-6 1202204
Folstein MF, Folstein SE, McHugh PR (1975) Mini-mental state. A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res 12:189–1981202204 10.1016/0022-3956(75)90026-6
23. Nasreddine ZS Phillips NA Bédirian V Charbonneau S Whitehead V Collin I The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment J Am Geriatr Soc 2005 53 695 699 10.1111/j.1532-5415.2005.53221.x 15817019
Nasreddine ZS, Phillips NA, Bédirian V, Charbonneau S, Whitehead V, Collin I et al (2005) The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc 53:695–69915817019 10.1111/j.1532-5415.2005.53221.x
24. Reitan RM Validity of the trail making test as an Indicator of Organic Brain damage Percept Mot Skills 1958 8 271 276 10.2466/pms.1958.8.3.271
Reitan RM (1958) Validity of the trail making test as an Indicator of Organic Brain damage. Percept Mot Skills 8:271–27610.2466/pms.1958.8.3.271
25. Rey A L’examen psychologique dans les cas d’encéphalopathie traumatique. (Les problems.). [The psychological examination in cases of traumatic encepholopathy Probl ] Archives de Psychologie 1941 28 215 285
Rey A (1941) L’examen psychologique dans les cas d’encéphalopathie traumatique. (Les problems.). [The psychological examination in cases of traumatic encepholopathy. Probl ] Archives de Psychologie 28:215–285
26. Zazzo R Le test des deux barrages Bull De Psychologie 1952 5 554 559 10.3406/bupsy.1952.6033
Zazzo R (1952) Le test des deux barrages. Bull De Psychologie 5:554–55910.3406/bupsy.1952.6033
27. Wechsler Adult Intelligence Scale–Third Edition. https://psycnet.apa.org/doiLanding?doi=10.1037%2Ft49755-000. Accessed 21 Aug 2023
28. Sánchez-Cubillo I Periáñez JA Adrover-Roig D Rodríguez-Sánchez JM Ríos-Lago M Tirapu J Construct validity of the trail making test: role of task-switching, working memory, inhibition/interference control, and visuomotor abilities J Int Neuropsychol Soc 2009 15 438 450 10.1017/S1355617709090626 19402930
Sánchez-Cubillo I, Periáñez JA, Adrover-Roig D, Rodríguez-Sánchez JM, Ríos-Lago M, Tirapu J et al (2009) Construct validity of the trail making test: role of task-switching, working memory, inhibition/interference control, and visuomotor abilities. J Int Neuropsychol Soc 15:438–45019402930 10.1017/S1355617709090626
29. Isaacs B Kennie AT The set test as an aid to the detection of dementia in old people Br J Psychiatry 1973 123 467 470 10.1192/bjp.123.4.467 4748864
Isaacs B, Kennie AT (1973) The set test as an aid to the detection of dementia in old people. Br J Psychiatry 123:467–4704748864 10.1192/bjp.123.4.467
30. Golden CJ Identification of brain disorders by the Stroop Color and Word Test J Clin Psychol 1976 32 654 658 10.1002/1097-4679(197607)32:3<654::AID-JCLP2270320336>3.0.CO;2-Z 956433
Golden CJ (1976) Identification of brain disorders by the Stroop Color and Word Test. J Clin Psychol 32:654–658956433 10.1002/1097-4679(197607)32:3<654::AID-JCLP2270320336>3.0.CO;2-Z
31. Belleville S Rouleau N Van der Linden M Use of the Hayling task to measure inhibition of prepotent responses in normal aging and Alzheimer’s disease Brain Cogn 2006 62 113 119 10.1016/j.bandc.2006.04.006 16757076
Belleville S, Rouleau N, Van der Linden M (2006) Use of the Hayling task to measure inhibition of prepotent responses in normal aging and Alzheimer’s disease. Brain Cogn 62:113–11916757076 10.1016/j.bandc.2006.04.006
32. Podsiadlo D Richardson S The timed up & go: a test of basic functional mobility for frail elderly persons J Am Geriatr Soc 1991 39 142 148 10.1111/j.1532-5415.1991.tb01616.x 1991946
Podsiadlo D, Richardson S (1991) The timed up & go: a test of basic functional mobility for frail elderly persons. J Am Geriatr Soc 39:142–1481991946 10.1111/j.1532-5415.1991.tb01616.x
33. Kaplan MH Feinstein AR The importance of classifying initial co-morbidity in evaluating the outcome of diabetes mellitus J Chronic Dis 1974 27 387 404 10.1016/0021-9681(74)90017-4 4436428
Kaplan MH, Feinstein AR (1974) The importance of classifying initial co-morbidity in evaluating the outcome of diabetes mellitus. J Chronic Dis 27:387–4044436428 10.1016/0021-9681(74)90017-4
34. Cruz-Jentoft AJ Bahat G Bauer J Boirie Y Bruyère O Cederholm T Sarcopenia: revised European consensus on definition and diagnosis Age Ageing 2019 48 601 10.1093/ageing/afz046 31081853
Cruz-Jentoft AJ, Bahat G, Bauer J, Boirie Y, Bruyère O, Cederholm T et al (2019) Sarcopenia: revised European consensus on definition and diagnosis. Age Ageing 48:60131081853 10.1093/ageing/afz046
35. Kalafat M Hugonot-Diener L Poitrenaud J The Mini Mental State (MMS): French standardization and normative data [Standardisation et étalonnage français du Mini Mental State (MMS) version GRÉCO] Revue De Neuropsychologie 2003 13 209 236
Kalafat M, Hugonot-Diener L, Poitrenaud J (2003) The Mini Mental State (MMS): French standardization and normative data [Standardisation et étalonnage français du Mini Mental State (MMS) version GRÉCO]. Revue De Neuropsychologie 13:209–236
36. Senior G Piovesana A Beaumont P Discrepancy analysis and Australian norms for the trail making test Clin Neuropsychol 2018 32 510 523 10.1080/13854046.2017.1357756 28752789
Senior G, Piovesana A, Beaumont P (2018) Discrepancy analysis and Australian norms for the trail making test. Clin Neuropsychol 32:510–52328752789 10.1080/13854046.2017.1357756
37. Bohannon RW Reference values for the timed up and go test: a descriptive meta-analysis J Geriatr Phys Ther 2006 29 64 68 10.1519/00139143-200608000-00004 16914068
Bohannon RW (2006) Reference values for the timed up and go test: a descriptive meta-analysis. J Geriatr Phys Ther 29:64–6816914068 10.1519/00139143-200608000-00004
38. Jolliffe I Lovric M Principal component analysis International Encyclopedia of Statistical Science 2011 Berlin, Heidelberg Springer 1094 1096
Jolliffe I (2011) Principal component analysis. In: Lovric M (ed) International Encyclopedia of Statistical Science. Springer, Berlin, Heidelberg, pp 1094–1096
39. Levasseur R Sabatier J-P Guilcher C Guaydier-Souquières G Costentin-Pignol V Jean-Jacques P-Y Medical management of patients over 50 years admitted to orthopedic surgery for low-energy fracture Joint Bone Spine 2007 74 160 165 10.1016/j.jbspin.2006.03.003 16987682
Levasseur R, Sabatier J-P, Guilcher C, Guaydier-Souquières G, Costentin-Pignol V, Jean-Jacques P-Y et al (2007) Medical management of patients over 50 years admitted to orthopedic surgery for low-energy fracture. Joint Bone Spine 74:160–16516987682 10.1016/j.jbspin.2006.03.003
40. Westlake KP Johnson BP Creath RA Neff RM Rogers MW Influence of non-spatial working memory demands on reach-grasp responses to loss of balance: effects of age and fall risk Gait Posture 2016 45 51 55 10.1016/j.gaitpost.2016.01.007 26979883
Westlake KP, Johnson BP, Creath RA, Neff RM, Rogers MW (2016) Influence of non-spatial working memory demands on reach-grasp responses to loss of balance: effects of age and fall risk. Gait Posture 45:51–5526979883 10.1016/j.gaitpost.2016.01.007
41. Collette F Angel L Mémoire et fonctions exécutives: nouvelles pistes de recherche Biol Aujourd’Hui 2015 209 287 294 10.1051/jbio/2015027 26820834
Collette F, Angel L (2015) Mémoire et fonctions exécutives: nouvelles pistes de recherche. Biol Aujourd’Hui 209:287–29426820834 10.1051/jbio/2015027
42. Liu-Ambrose T Ahamed Y Graf P Feldman F Robinovitch SN Older fallers with poor working memory overestimate their postural limits Arch Phys Med Rehabil 2008 89 1335 1340 10.1016/j.apmr.2007.11.052 18586136
Liu-Ambrose T, Ahamed Y, Graf P, Feldman F, Robinovitch SN (2008) Older fallers with poor working memory overestimate their postural limits. Arch Phys Med Rehabil 89:1335–134018586136 10.1016/j.apmr.2007.11.052
43. Butts KA Floresco SB Phillips AG Acute stress impairs set-shifting but not reversal learning Behav Brain Res 2013 252 222 229 10.1016/j.bbr.2013.06.007 23764458
Butts KA, Floresco SB, Phillips AG (2013) Acute stress impairs set-shifting but not reversal learning. Behav Brain Res 252:222–22923764458 10.1016/j.bbr.2013.06.007
44. Langeard A Pothier K Morello R Lelong-Boulouard V Lescure P Bocca M-L Polypharmacy Cut-Off for Gait and cognitive impairments Front Pharmacol 2016 7 296 10.3389/fphar.2016.00296 27630572
Langeard A, Pothier K, Morello R, Lelong-Boulouard V, Lescure P, Bocca M-L et al (2016) Polypharmacy Cut-Off for Gait and cognitive impairments. Front Pharmacol 7:29627630572 10.3389/fphar.2016.00296
45. Attoh-Mensah E Loggia G Schumann-Bard P Morello R Descatoire P Marcelli C Adverse effects of anticholinergic drugs on Cognition and mobility: cutoff for impairment in a cross-sectional study in young-old and old-old adults Drugs Aging 2020 37 301 310 10.1007/s40266-019-00743-z 31930459
Attoh-Mensah E, Loggia G, Schumann-Bard P, Morello R, Descatoire P, Marcelli C et al (2020) Adverse effects of anticholinergic drugs on Cognition and mobility: cutoff for impairment in a cross-sectional study in young-old and old-old adults. Drugs Aging 37:301–31031930459 10.1007/s40266-019-00743-z
46. Loggia G Attoh-Mensah E Pothier K Morello R Lescure P Bocca M-L Psychotropic polypharmacy in adults 55 years or older: a risk for impaired global cognition, executive function, and mobility Front Pharmacol 2019 10 1659 10.3389/fphar.2019.01659 32082159
Loggia G, Attoh-Mensah E, Pothier K, Morello R, Lescure P, Bocca M-L et al (2019) Psychotropic polypharmacy in adults 55 years or older: a risk for impaired global cognition, executive function, and mobility. Front Pharmacol 10:165932082159 10.3389/fphar.2019.01659
47. Høiberg MP Rubin KH Hermann AP Brixen K Abrahamsen B Diagnostic devices for osteoporosis in the general population: a systematic review Bone 2016 92 58 69 10.1016/j.bone.2016.08.011 27542659
Høiberg MP, Rubin KH, Hermann AP, Brixen K, Abrahamsen B (2016) Diagnostic devices for osteoporosis in the general population: a systematic review. Bone 92:58–6927542659 10.1016/j.bone.2016.08.011
