
==== Front
Lipids Health Dis
Lipids Health Dis
Lipids in Health and Disease
1476-511X
BioMed Central London

2306
10.1186/s12944-024-02306-7
Research
Association between triglyceride glucose body mass index and urinary incontinence: a cross-sectional study from the National Health and Nutrition Examination Survey (NHANES) 2001 to 2018
Li JiHang 1
Xie Ruijie 2
Tian Hu 1
Wang Dong 1
Mo MingShen 1
Yang JianKun 592053507@qq.com

1
Guo WenBin gwb200350514@163.com

1
1 https://ror.org/0050r1b65 grid.413107.0 Department of Urology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, 510630 China
2 https://ror.org/03mqfn238 grid.412017.1 0000 0001 0266 8918 Department of Hand & Foot Surgery, Hengyang Medical School, The Affiliated Nanhua Hospital, University of South China, Hengyang, 421002 China
20 9 2024
20 9 2024
2024
23 3044 5 2024
17 9 2024
© The Author(s) 2024
2024
https://creativecommons.org/licenses/by-nc-nd/4.0/ Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.
Background

Urinary incontinence (UI) is a prevalent, health-threatening condition that causes isolation and psychological strain, leading to significant personal distress. The connection between the triglyceride glucose body mass index (TyG-BMI) and UI remains elusive. The purpose of the current research was to investigate any possible relationships between raised TyG-BMI levels and a higher likelihood of UI.

Methods

For a thorough examination, adults 20 years and older with UI were included in cross-sectional research using the data obtained from the National Health and Nutrition Examination Survey (NHANES) from 2001 to 2018. Our investigation centred on three of the significant varieties of UI: Urgent Urinary Incontinence (UUI), Mixed Urinary Incontinence (MUI), and Stress Urinary Incontinence (SUI), employing weighted multivariate logistic regression models for an in-depth evaluation. The TyG-BMI, a possible biomarker, was arranged in increasing order among participants and then assessed with a trend test (P for trend). Moreover, this investigation delved into the non-linear relationships using advanced smoothed curve fitting techniques. Meticulous subgroup analyses were executed to verify the uniformity of the UI and TyG-BMI relationship across diverse demographic groups.

Results

A thorough investigation was conducted with 18,751 subjects to analyze the prevalence and types of UI, showing that 23.59% of individuals suffered from SUI, 19.42% from UUI, and 9.32% from MUI. Considering all possible confounding variables, Multivariate logistic regression analysis showed a substantial relationship between elevated TyG-BMI values and a greater likelihood across all UI categories. Specifically, stratifying the TyG-BMI into quartiles revealed a pronounced positive correlation in the top quartile relative to the bottom, reflected in increased odds ratios for SUI, UUI, and MUI (SUI: OR = 2.36, 95% CI 2.03–2.78, P < 0.0001; UUI: OR = 1.86, 95% CI 1.65–2.09, P < 0.0001; MUI: OR = 2.07, 95% CI 1.71–2.51, P < 0.0001).

Conclusions

Among US adults, an association has been observed wherein increased TyG-BMI values correlate with a higher chance of UI. This suggests that TyG-BMI might be a helpful marker for identifying individuals at risk of UI, providing novel insights into its assessment and management.

Keywords

Triglyceride glucose body mass index
Urinary incontinence
Insulin resistance
Cross-sectional study
NHANES
issue-copyright-statement© BioMed Central Ltd., part of Springer Nature 2024
==== Body
pmcBackground

The condition known as urinary incontinence, distinguished by involuntary urinary outflow, constitutes a widespread medical condition predominantly affecting women [1]. It may pose challenges to physical, social, mental, and emotional well-being [2]. The three types of UI, symptomatically classified, are mixed (MUI), stress (SUI), and urge (UUI). Global statistics show a yearly rise in the overall incidence of UI in females, with rates of occurrence varying from 25 to 45% [3]. Similarly, research on male prevalence in the US demonstrates that UI prevalence escalates from 11% in males aged 60–64 to 31% among individuals aged 85 and older [4]. Numerous individuals remain unaware of this global health challenge, resulting in delayed diagnosis and treatment. UI can stem from a variety of factors, among which metabolic syndrome (METS) is directly linked to its onset and progression [5].

Dyslipidemia, obesity, hypertension, and insulin resistance are the clinical conditions that define METS [6]. However, the most significant contributor to METS's progression is insulin resistance [7]. In a study including 184 female patients, Uzun H et al. [8] identified a correlation between insulin resistance (IR) and overactive bladder syndrome (OAB), which leads to an increased incidence of UI. Due to their complexity and challenging implementation, conventional IR metrics such as the homeostasis model assessment (HOMA-IR) and the hyperinsulinemic-euglycemic clamp (HIEC) are impractical for clinical application [9]. The utilization of TyG-BMI is suggested to be an efficient and convenient substitute that may indicate the presence of IR [10]. Comprehensive research has confirmed that diabetes, hypertension, stroke, heart disease, and fatty liver disease, among others, exhibit a correlation with TyG-BMI [11–17].

Present research often overlooks the combined impacts of various metabolic variables to concentrate solely on a single element, such as the relationship between diabetes or obesity and UI. Studies on UI conducted so far have mainly examined anatomical, physiological, and neural factors; however, a thorough examination of the impact of metabolic parameters, particularly comprehensive metabolic indicators, has yet to be thoroughly discussed. This study examines the connection between UI and TyG-BMI for the first time. TyG-BMI could be linked to a higher incidence of UI.

Methods

Data source and participants

The data utilized in this cross-sectional study were obtained from the National Health and Nutrition Examination Survey (NHANES), a dataset specifically developed to evaluate the health conditions and nutritional status of the general population of the United States. NHANES gathers information on various aspects such as population characteristics, financial status, and public health to assess the overall well-being of the population [18]. At the https://www.cdc.gov/nchs/nhanes/ , the public can access the exhaustive NHANES dataset and research methodology. The present investigation followed the cross-sectional research guidelines established by the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) [19]. Data spanning nine cycles (2001–2018) from the NHANES database were analyzed. To deal with missing values in the data, we used multiple imputation method. Initially, 91,351 individuals were recruited. Exclusions included participants under 20 years (n = 41,150), those with incomplete UI data (n = 6,365), those lacking BMI, triglyceride, and fasting glucose data (n = 24,593), and pregnant individuals (n = 492). Ultimately, the study comprised 18,751 participants (Fig. 1). The NHANES data used in this study were collected in strict accordance with standard operating procedures. Intra-assay variability was minimized by performing repeated measurements under the same conditions, while inter-assay variability was reduced through standardized procedures and equipment calibration across cycles. We also applied sample weighting and multiple imputation methods in our analysis to further enhance the reliability of the results.Fig. 1 Flowchart of participants selection from NHANES 2001–2018

Exposure and outcome definitions

The exposure variable was defined as TyG-BMI, which was computed by the following formula: Ln [triglycerides (mg/dl) * fasting blood glucose (mg/dl)/2] * BMI (kg/m2) [17]. Triglycerides were enzymatically measured using the spectrophotometric method (Roche Cobas 6000 chemical analyzer), while plasma glucose concentrations were determined using the glucose-oxidase method (Roche/Hitachi Cobas C 501 chemical analyzer).

By assessing the NHANES data, the incidence of UI was determined in the current research, focusing on two questionnaire items related to bladder function. SUI was identified in participants reporting involuntary urine leakage in small amounts due to physical activities, including coughing or exercise, within the past year. UUI was distinguished by the concurrent presence of involuntary urine discharge and an urgent, compelling urge to urinate during the same period. Individuals reporting symptoms of both SUI and UUI were categorized as having MUI, offering a comprehensive classification of UI subtypes in the cohort.

Assessment of covariates of interest

This research assessed vital variables such as age, gender, ethnicity, educational attainment (divided into under high school, high school, and above high school), household income (as determined by the ratio of family income to poverty, which is classified as follows: < 1.3, 1.3–3.5, and > 3.5), the calculation of family poverty ratios was based on the Family Income Poverty Guidelines provided by the US Department of Health and Human Services (DHHS) [20], marital status (with classifications of single, married, living together, widowed, divorced, or separated), smoking status (non-smokers, current smokers, and individuals who have inhaled at least 100 cigarettes in their lifetime but do not smoke at present), alcohol consumption (categorized into ≥ 12 alcoholic beverages annually and non-consumers), diabetes mellitus (identified by physician diagnosis, use of anti-diabetic medication, or an HbA1c > 6.5%), hypertension (defined by physician diagnosis, medication usage, or blood pressure readings > 140/90 mmHg), and high cholesterol. High cholesterol was determined if a physician diagnosed participants used hypercholesterolemia medication, or had a total cholesterol measurement of ≥ 240 mg/dL. Participants were asked if they had health insurance or a different healthcare plan to determine their coverage.

Statistical analysis

Statistical analyses followed CDC guidelines and included NHANES sample weights. Consequently, logistic regression was employed to extrapolate categorical parameters to proportions, while linear regression facilitated the generalization of continuous variables to means with accompanying standard deviations (SD). This study utilized three distinct multivariate logistic regression models to elucidate the connection between TyG-BMI and UI. The models varied in covariate adjustments: Model 1 did not include any covariate modifications, while Model 2 included age, gender, and race. In contrast, Model 3 integrated covariates, including age, gender, education level, alcohol use, family poverty ratio, race/ethnicity, vigorous activity, moderate activity, marital status, smoking status, diabetes, high cholesterol, hypertension and health insurance coverage.

Additionally, TyG-BMI was categorized into quartiles from a continuous measure, enabling a trend analysis to identify potential correlations with UI. Smooth curve fitting methods were used to assess the non-linear correlation. A stratified subgroup analysis, employing hierarchical multiple regression analysis with an interaction term, was conducted to explore heterogeneity among subgroups. By analyzing receiver-operating characteristic (ROC) curves and computing the area under the curve (AUC), it was possible to evaluate TyG-BMI's discriminatory ability in predicting the three kinds of UI. Statistical analyses were performed using R software version 3.4.3 from The R Foundation and Empower software (X&Y Solutions, Inc., Boston, MA, USA). A p-value of less than 0.05 was considered statistically significant.

Results

Characteristics of the participants

The demographic characteristics and other factors are shown in Table 1, categorized by TyG-BMI quartiles. The study included 18,751 participants, with an average age of 50.30 ± 17.80 years, split almost evenly between females (49.45%) and males (50.55%) based on weighted proportions. Table 1 Basic characteristics of participants by TyG-BMI among U.S. adults

TyG-BMI	Overall	Q1	Q2	Q3	Q4	P-value	
N = 18,751	(112.58–204.87)	(204.87–242.54)	(242.54–287.23)	(287.23–679.46)	
N = 4688	N = 4687	N = 4688	N = 4688	
Age(year), Mean ± SD	50.30 ± 17.80	45.37 ± 19.16	52.24 ± 17.96	52.37 ± 17.16	51.24 ± 15.82	 < 0.001	
Gender, n(%)						 < 0.001	
 Male	9478 (50.55%)	2120 (45.22%)	2620 (55.90%)	2597 (55.40%)	2141 (45.67%)		
 Female	9273 (49.45%)	2568 (54.78%)	2067 (44.10%)	2091 (44.60%)	2547 (54.33%)		
Race, n(%)						 < 0.001	
 Mexican American	3148 (16.79%)	492 (10.49%)	797 (17.00%)	938 (20.01%)	921 (19.65%)		
 Other Hispanic	1619 (8.63%)	322 (6.87%)	439 (9.37%)	451 (9.62%)	407 (8.68%)		
 Non-Hispanic White	8597 (45.85%)	2299 (49.04%)	2149 (45.85%)	2045 (43.62%)	2104 (44.88%)		
 Non-Hispanic Black	3697 (19.72%)	893 (19.05%)	840 (17.92%)	924 (19.71%)	1040 (22.18%)		
 Other Races	1690 (9.01%)	682 (14.55%)	462 (9.86%)	330 (7.04%)	216 (4.61%)		
Education level, n(%)						 < 0.001	
 Less than high school	4787 (25.55%)	965 (20.60%)	1208 (25.81%)	1286 (27.46%)	1328 (28.34%)		
 High school or GED	4375 (23.35%)	1019 (21.75%)	1061 (22.67%)	1165 (24.88%)	1130 (24.11%)		
 Above high school	9572 (51.09%)	2701 (57.65%)	2411 (51.52%)	2232 (47.66%)	2228 (47.55%)		
Marital status, n(%)						 < 0.001	
 Married or living with partners	11,394 (60.79%)	2587 (55.20%)	2930 (62.53%)	3017 (64.38%)	2860 (61.05%)		
 Widowed, divorced, or separated	4137 (22.07%)	874 (18.65%)	1072 (22.88%)	1060 (22.62%)	1131 (24.14%)		
 Never married	3213 (17.14%)	1226 (26.16%)	684 (14.60%)	609 (13.00%)	694 (14.81%)		
Family poverty ratio, n(%)						 < 0.001	
 < 1.3	5078 (29.39%)	1226 (28.39%)	1196 (27.63%)	1217 (28.22%)	1439 (33.33%)		
 1.3–3.5	6717 (38.88%)	1600 (37.05%)	1714 (39.59%)	1723 (39.95%)	1680 (38.91%)		
  ≥ 3.5	5483 (31.73%)	1492 (34.55%)	1419 (32.78%)	1373 (31.83%)	1199 (27.77%)		
Alcohol use, n(%)						 < 0.001	
 Yes	13,793 (73.76%)	3505 (74.91%)	3539 (75.81%)	3474 (74.33%)	3275 (69.99%)		
 No	4907 (26.24%)	1174 (25.09%)	1129 (24.19%)	1200 (25.67%)	1404 (30.01%)		
Smoking status, n(%)						 < 0.001	
 Never	9953 (53.12%)	2600 (55.50%)	2463 (52.62%)	2453 (52.35%)	2437 (52.03%)		
 Past	4825 (25.75%)	893 (19.06%)	1244 (26.58%)	1336 (28.51%)	1352 (28.86%)		
 Current	3958 (21.13%)	1192 (25.44%)	974 (20.81%)	897 (19.14%)	895 (19.11%)		
Hypertension, n(%)						 < 0.001	
 Yes	8182 (43.64%)	1214 (25.90%)	1893 (40.41%)	2253 (48.07%)	2822 (60.20%)		
 No	10,565 (56.36%)	3473 (74.10%)	2792 (59.59%)	2434 (51.93%)	1866 (39.80%)		
Diabetes, n(%)						 < 0.001	
 Yes	2900 (15.47%)	179 (3.82%)	494 (10.54%)	761 (16.24%)	1466 (31.27%)		
 No	15,850 (84.53%)	4509 (96.18%)	4193 (89.46%)	3926 (83.76%)	3222 (68.73%)		
High cholesterol, n(%)						 < 0.001	
 Yes	7659 (40.85%)	1193 (25.45%)	1936 (41.31%)	2164 (46.16%)	2366 (50.47%)		
 No	11,092 (59.15%)	3495 (74.55%)	2751 (58.69%)	2524 (53.84%)	2322 (49.53%)		
Health insurance coverage, n(%)						0.003	
 Yes	14,710 (78.66%)	3615 (77.34%)	3680 (78.75%)	3653 (78.16%)	3762 (80.38%)		
 No	3991 (21.34%)	1059 (22.66%)	993 (21.25%)	1021 (21.84%)	918 (19.62%)		
Vigorous physical activity, n(%)						 < 0.001	
 Yes	4530 (24.16%)	1554 (33.15%)	1204 (25.69%)	1047 (22.34%)	725 (15.47%)		
 No	14,219 (75.84%)	3134 (66.85%)	3482 (74.31%)	3640 (77.66%)	3963 (84.53%)		
Moderate physical activity, n(%)						 < 0.001	
 Yes	8131 (43.38%)	2282 (48.68%)	2099 (44.83%)	1986 (42.38%)	1764 (37.63%)		
 No	10,613 (56.62%)	2406 (51.32%)	2583 (55.17%)	2700 (57.62%)	2924 (62.37%)		
 TG (mg/dl), Mean ± SD	132.44 ± 120.73	79.33 ± 39.48	112.88 ± 63.48	146.64 ± 88.18	190.89 ± 195.25	 < 0.001	
 FBG (mg/dl), Mean ± SD	109.15 ± 36.22	95.99 ± 15.92	104.09 ± 26.67	110.25 ± 33.16	126.26 ± 51.87	 < 0.001	
 BMI (kg/m2), Mean ± SD	28.95 ± 6.66	22.05 ± 2.18	26.28 ± 1.85	29.92 ± 2.27	37.55 ± 5.86	 < 0.001	
SUI, n(%)						 < 0.001	
 No	14,399 (76.79%)	3851 (82.15%)	3717 (79.30%)	3628 (77.39%)	3203 (68.32%)		
 Yes	4352 (23.21%)	837 (17.85%)	970 (20.70%)	1060 (22.61%)	1485 (31.68%)		
UUI, n(%)						 < 0.001	
 No	14,487 (77.26%)	3906 (83.32%)	3717 (79.30%)	3616 (77.13%)	3248 (69.28%)		
 Yes	4264 (22.74%)	782 (16.68%)	970 (20.70%)	1072 (22.87%)	1440 (30.72%)		
MUI, n(%)						 < 0.001	
 No	16,781 (89.49%)	4380 (93.43%)	4269 (91.08%)	4200 (89.59%)	3932 (83.87%)		
 Yes	1970 (10.51%)	308 (6.57%)	418 (8.92%)	488 (10.41%)	756 (16.13%)		
Mean ± SD for continuous variables: the P value was calculated by the weighted linear regression model; n (%) for categorical variables: the P value was calculated by the weighted chi-square test

Abbreviation: TyG-BMI Triglyceride glucose body mass index, TG triglyceride, FBG fasting blood glucose, BMI body mass index, SUI Stress Urinary incontinence, UUI Urge urinary incontinence, MUI Mixed urinary incontinence

Among the participants, 23.21% self-reported previous SUI, 22.74% reported UUI, and 10.51% reported MUI. The designated quartiles for triglyceride-glucose body mass index were Q1 (112.58–204.87), Q2 (204.87–242.54), Q3 (242.54–287.23), and Q4 (287.23–679.46). A substantial rise in the incidence of UI was linked to higher TyG-BMI categories. Additionally, individuals in the upper TyG-BMI quartile were more inclined to be women, white, possess advanced education, be married or cohabiting, experience middle household poverty rates, consume alcohol, have elevated blood pressure, and engage in lower levels of physical activity.

Correlation of TyG-BMI with the likelihood of urinary incontinence (SUI, UUI, MUI)

The correlation between TyG-BMI and the likelihood of developing UI is shown in Table 2. Weighted multivariate logistic regression was used, adjusting models in a tiered approach: unadjusted (Model 1), moderately adjusted (Model 2), and fully adjusted (Model 3) for a precise assessment of the relationship. This research revealed that the three forms of UI had substantially greater likelihoods linked with increasing TyG-BMI values. Table 2 Associations between TyG-BMI and urinary incontinence

SUI	OR (95% CI), P-value	
Model 1	Model 2	Model 3	
Continuous	1.00 (1.00,1.01),

 < 0.0001

	1.01 (1.00,1.03),

 < 0.0001

	1.01 (1.00,1.01),

 < 0.0001

	
Categories				
Q1	Reference	Reference	Reference	
Q2	1.21 (1.08,1.33),

0.0005

	1.36 (1.17,1.59),

 < 0.0001

	1.38 (1.17,1.62),

 < 0.0001

	
Q3	1.34 (1.21,1.49),

 < 0.0001

	1.53 (1.33,1.77),

 < 0.0001

	1.49 (1.25,1.71),

 < 0.0001

	
Q4	1.86 (1.63,2.11),

 < 0.0001

	2.46 (2.14,2.84),

 < 0.0001

	2.36 (2.03,2.78),

 < 0.0001

	
P for trend	 < 0.001	 < 0.001	 < 0.001	
UUI	OR (95% CI), P-value	
Model 1	Model 2	Model 3	
Continuous	1.00 (1.00,1.01),

 < 0.0001

	1.01 (1.00,1.02),

 < 0.0001

	1.01 (1.00,1.01),

 < 0.0001

	
Categories				
Q1	Reference	Reference	Reference	
Q2	1.26 (1.11,1.43),

0.0011

	1.13 (0.97,1.31),

0.1076

	1.19 (1.06,1.334),

0.0042

	
Q3	1.35 (1.17,1.55),

 < 0.0001

	1.23 (1.05,1.43),

 < 0.0101

	1.28 (1.14,1.44),

 < 0.0001

	
Q4	2.01 (1.76,2.28),

 < 0.0001

	1.82 (1.58,2.08),

 < 0.0001

	1.86 (1.65,2.09),

 < 0.0001

	
P for trend	 < 0.001	 < 0.001	 < 0.001	
MUI	OR (95% CI), P-value	
Model 1	Model 2	Model 3	
Continuous	1.01 (1.00,1.01),

 < 0.0001

	1.00 (1.00,1.01),

 < 0.0001

	1.01 (1.00,1.02),

 < 0.0001

	
Categories				
Q1	Reference	Reference	Reference	
Q2	1.32 (1.11,1.59),

0.0034

	1.38 (1.13,1.69),

0.0017

	1.34 (1.09,1.65),

0.0004

	
Q3	1.47 (1.22,1.78),

 < 0.0001

	1.62 (1.32,1.94),

 < 0.0001

	1.41 (1.12,1.76),

 < 0.0001

	
Q4	2.38 (2.01,2.84),

 < 0.0001

	2.46 (2.03,2.98),

 < 0.0001

	2.07 (1.71,2.51),

 < 0.0001

	
P for trend	 < 0.001	 < 0.001	 < 0.001	
Model 1: unadjusted

Model 2: adjusted for age, gender and race/ethnicity

Model 3: adjusted for variables, including age, gender, race/ethnicity, education level, marital status, the family poverty ratio, smoking status, alcohol use, vigorous activity, moderate activity, diabetes, hypertension, high cholesterol, and health insurance coverage

Abbreviation: TyG-BMI Triglyceride glucose body mass index, SUI Stress Urinary incontinence, UUI Urge urinary incontinence, MUI Mixed urinary incontinence, OR odds ratio, 95%CI 95% confidence interval

The likelihood of UI and TyG-BMI all exhibited statistically significant positive connections in all three different adjusted models, with statistical significance confirmed (P < 0.0001). For additional validation, the TyG-BMI variable was analyzed as a continuous variable in categorical form, dividing the cohort into quartiles (Q1–Q4). Individuals in the top quartile (Q4) had a much higher probability of experiencing any UI compared to those in the bottom quartile (Q1). This association remained significant in all three different adjusted models: unadjusted (SUI: OR = 1.86; 95% CI = 1.63–2.11, UUI: OR = 2.01; 95% CI = 1.76–2.28, MUI: OR = 2.38; 95% CI = 2.01–2.84); moderately adjusted (SUI: OR = 2.46; 95% CI = 2.14–2.84, UUI: OR = 1.82; 95% CI = 1.58–2.08, MUI: OR = 2.46; 95% CI = 2.03–2.98); and fully adjusted (SUI: OR = 2.36; 95% CI = 2.03–2.78, UUI: OR = 1.86; 95% CI = 1.65–2.09, MUI: OR = 2.07; 95% CI = 1.71–2.51).

Further investigation of the relationship between UI likelihood and TyG-BMI, employing smoothed curve fitting techniques, verified a statistically significant, consistent positive relationship across all three models (Fig. 2).Fig. 2 Smooth curve fitting for the relationship between TyG-BMI and three UI types. A, B, and C represent the linear associations between TyG-BMI and SUI, UUI, and MUI, respectively. The solid red line represents the smooth curve fit between variables. Blue bands represent the 95% confidence interval from the fit. The Y-axis represents the probability of occurrence of each of the three UI types

Subgroup analysis

In this study, subgroup analyses were conducted, and interactions within diverse demographic segments were tested to assess the robustness of the UI and TyG-BMI association. Notably, gender was found to modulate the link between SUI and TyG-BMI, with a more pronounced association observed in females than in males, as evidenced by a significant interaction term (P < 0.05) (Fig. 3A). Conversely, gender-based analyses for UUI and MUI failed to reveal significant differences, with all interaction P-values exceeding 0.05 (Fig. 3B and C). Furthermore, subgroup evaluations across various classifications did not significantly alter the positive connection between UI and TyG-BMI, affirming the consistency across all examined cohorts.Fig. 3 Subgroup analysis of the association between TyG-BMI and three UI types. A, B and C represent the subgroup analysis results for the relationships between TyG-BMI and SUI, UUI, and MUI in different stratifications

The ROC curve of TyG-BMI for the UI

The relationship between TyG-BMI and the risk of UI (SUI, MUI, UUI) was assessed using the ROC curve. Figure 4 shows that the association of TyG-BMI with the risk of UI is indicated by AUC values for SUI (AUC = 0.828, 95% CI 0.822–0.835), MUI (AUC = 0.806, 95% CI 0.797–0.816), and UUI (AUC = 0.744, 95% CI 0.735–0.752). Table 3 provides detailed information on the performance of TyG-BMI in predicting the three types of UI, including cutoff values, sensitivity, and specificity. For SUI, the optimal cutoff value was 1.164, yielding a sensitivity of 69.4% and a specificity of 86.3%. In the case of MUI, the cutoff value was 2.193, with corresponding sensitivity and specificity values of 70.3% and 77.5%, respectively. For UUI, the optimal cutoff value was 1.262, with a sensitivity of 66.1% and a specificity of 70.6%. These cutoff points represent the optimal thresholds between the TyG-BMI index and UI risk.Fig. 4 Receiver operating characteristic (ROC) curve analysis for assessing the association with UI. A TyG-BMI was assessed to identify SUI. B TyG-BMI was assessed to identify MUI. (C) TyG-BMI was assessed to identify UUI

Table 3 The TyG-BMI for assessing the association with three types of UI

Test	AUC	95%CI low	95%CI upp	Cut-off value	Specificity	Sensitivity	
SUI	
TyG-BMI	0.828	0.822	0.835	1.164	0.863	0.694	
UUI	
TyG-BMI	0.744	0.735	0.752	1.262	0.706	0.661	
MUI	
TyG-BMI	0.806	0.797	0.816	2.193	0.775	0.703	
AUC area under curve, 95% CI 95% confidence interval

Discussion

This investigation elucidates the relationship between UI and the TyG-BMI in a diverse cohort of US citizens, analyzing NHANES data from 2001 to 2018. Our findings show a robust correlation between higher TyG-BMI values and a higher chance of developing several types of UI, such as SUI, UUI, and MUI. Converting TyG-BMI from a numerical to a grouped variable by dividing it into quartiles confirmed the strong connection between increases in TyG-BMI and susceptibility to UI. Subgroup analyses further revealed a pronounced predisposition for SUI in females over males, underscoring the potential gender-specific impacts of TyG-BMI on UI. The possible reason for the differences in subgroup analyses is that pregnancy, childbirth, and the decline in estrogen in menopausal women can cause damage to the pelvic support structures and atrophy of the tissues around the vesico-urethral area in women [1, 2], all of which increase the risk of SUI in women. Secondly, UUI is often associated with overactive bladder (OAB), and the primary cause of OAB is abnormal contractions of the detrusor muscle. This process is regulated by the autonomic nervous system, which functions similarly in both males and females. Hence, gender has a lesser impact on UUI [21, 22].

We found that an elevated TyG-BMI is associated with a higher incidence of UI, consistent with previous studies linking IR with UI. For example, Uzun et al. demonstrated a correlation between IR and OAB in women, indicating that IR increases the incidence of urgency [8]. Furthermore, Nazzal et al. found that the significantly higher incidence of UI in women with diabetes is related to IR [23]. Our study further validates this association by using TyG-BMI as a surrogate marker for IR in evaluating UI. Compared to TyG, the TyG-BMI index, by incorporating weight factors, provides a more comprehensive assessment of metabolic status.

The underlying pathophysiology is hypothesized to involve IR, a pivotal factor in metabolic syndrome, contributing to UI onset via mechanisms related to inflammation, neuronal disruption, oxidative stress, and alterations in muscle mass and functionality [24].

Identifying straightforward and clinically valuable indicators of IR has garnered significant interest due to the costly and cumbersome nature of the HIEC procedures for diagnosing IR [17]. The HOMA-IR is another often utilized technique for measuring IR. It is a non-invasive method for studying IR, but it is insulin-dependent and has limited utility in patients on insulin therapy or without functional β cells [25]. Therefore, there are few application situations for either approach, mostly due to the rarity of measuring fasting insulin levels in typical clinical settings and extensive epidemiological research. Within this context, Prof. Er first introduced the TyG-BMI in 2016 [10]—a composite variable comprising fasting plasma glucose (FPG), triglycerides (TG), and body mass index (BMI). TyG-BMI offers a more straightforward and economical way to evaluate IR. It may be used for any patient, regardless of whether they are receiving insulin therapy, and does not require the measurement of insulin.

According to recent research, the TyG-BMI is a more accurate indicator of IR, surpassing traditional measures such as the Triglyceride-Glucose (TyG) index, BMI, visceral adiposity index, lipid accumulation products, adipokines, and lipid ratios [10]. Findings showed that the TyG-BMI performed better in IR prediction than the TyG index [26]. Moreover, the application of TyG-BMI extends across diverse clinical contexts, highlighting its versatility. For instance, Yang X et al. [12] demonstrated that TyG-BMI and the severity of coronary artery disease (CAD) in females have a direct linear connection, while Du Z et al. [27] highlighted its substantial correlation with ischemic stroke and suggested its utility in refining risk stratification for these conditions. In a population-based study, HOMA-IR and the TyG index were less effective than the TyG-BMI [28]. Additionally, the TyG-BMI has been independently associated with osteoporotic fractures and non-small cell lung cancer (NSCLC), underscoring its potential to predict a broad spectrum of diseases beyond metabolic disorders [29, 30]. In summary, the TyG-BMI represents a practical and potent tool for identifying and assessing IR and its associated risks across diverse diseases.

Additionally, TyG-BMI is also closely associated with pre-hypertension, diabetes, all-cause mortality in patients suffering from atrial fibrillation, and non-alcoholic fatty liver disease [13, 31, 32]. Nevertheless, studies investigating the correlation between UI and TyG-BMI are scarce. The problem of UI may cause great suffering among a wide range of people, especially women and the elderly. Nonetheless, few markers exist that can reliably predict the onset of UI. The clinical application of TyG-BMI could, to some extent, reduce the incidence of UI by facilitating early intervention and health counselling for high-risk populations.

One fundamental process associated with IR is oxidative stress. Mitochondrial dysfunction, characterized by reduced mitochondrial size and DNA content that elevates oxidative stress, represents a primary pathogenic feature of IR [33]. Additionally, insulin regulates oxidative capacity and mitochondrial metabolism through PI3K/Akt signalling [34, 35]. The induction of oxidative stress in the bladder suggests that IR could likewise provoke oxidative damage within the urethral sphincter, potentially altering the functionality of the lower urinary tract [36]. Blaha I et al. showed that IR correlates with higher levels of cellular injury caused by oxidative stress. Furthermore, elevated oxidative stress and diminished blood flow to the bladder could lead to neurological dysfunction of the bladder and injury to the urethral muscle cells, culminating in urinary urgency [37]. These findings offer additional support for the distinct correlation between IR and UI. Moreover, mitochondrial damage leads to significant production of reactive oxygen species (ROS), which subsequently leads to higher levels of inflammatory cytokines, hindering the function of pancreatic β-cells, worsening IR, and starting a harmful cycle of IR, mitochondrial damage, and inflammation [38, 39].

To our knowledge, prior research has established a correlation between inflammation and IR, and numerous studies have demonstrated that IR is positively correlated with high-sensitivity C-reactive protein [40–43]. Research involving ischemic stroke patients without diabetes also corroborated this association [44]. Moreover, IR not only diminishes enzyme activity in adipocytes but also activates the NLRP3 inflammasome, thereby leading to increased levels of inflammatory molecules like TNF-α and IL-6, which initiate the inflammatory process [45, 46]. Furthermore, although inflammation is both a cause and a result of insulin resistance, known to exacerbate each other cyclically [47], their synergistic role in driving UI still requires further investigation. And, their synergistic contribution to the pathophysiology of UI may involve complex multifactorial pathways. The study revealed that the inflammatory cytokine TNF-α impeded myogenic differentiation in human urethral transverse sphincter cells. This indicates that TNF-α could potentially elevate the likelihood of SUI among older individuals [48]. Moreover, overactive bladder syndrome (OAB) and UI, conditions exacerbated by inflammation, were studied. According to research by Chung SD et al. [22], individuals with OAB exhibited significantly elevated levels of CRP compared to those without OAB.

IR is strongly associated with the start of diabetes and is a significant contributor to the risk of the disease's progression [49, 50]. On the other hand, Nazzal Z et al. have indicated that diabetes significantly enhances the likelihood of UI. Among the 400 diabetic females in the study, 44%, aged 30–83, reported UI [23]. Furthermore, compared to females without Type 2 Diabetes Mellitus (T2DM), the prevalence of UI is considerably greater in females with T2DM, according to many research findings [51, 52].

The TyG-BMI, an adapted index derived from both BMI and TyG, is designed to assess the association with the incidence of UI more accurately. The potential benefits of TyG-BMI in relation to UI lie in its simple calculation method, which requires only routine physical examination data. Additionally, as an important assessment tool for IR, TyG-BMI can indirectly reflect the risk of UI. Our study presents multiple advantages. In order to increase the study's representativeness, we considered sample weights when analyzing NHANES data. Furthermore, adjustments were made for several confounding variables to bolster the data's reliability. Given the cross-sectional nature of our study, establishing causation was beyond our reach. Secondly, Self-reporting of UI is indeed the main means of obtaining disease diagnosis information, so the application and promotion of TyG-BMI does have limitations to a certain extent. Furthermore, despite accounting for numerous factors, the potential influence of additional confounders could only partially be excluded. Additionally, due to limitations inherent in the NHANES database's UI questionnaire design, symptoms and medical information for all three UI types were self-reported through interview responses, potentially reducing the count of verifiable UI cases. Given the reliance on NHANES database data, further high-quality cohort studies are necessary to support this connection.

Conclusions

The results of this investigation showed a correlation between elevated TyG-BMI levels and an increased risk of UI, a relationship that persisted even after adjusting for multiple covariates. We speculated that TyG-BMI could be used as a valuable clinical indicator. To confirm this relationship, additional prospective studies will be essential in the coming years.

Abbreviations

NHANES National Health and Nutrition Examination Survey

TyG-BMI Triglyceride glucose body mass index

UI Urinary incontinence

SUI Stress Urinary incontinence

UUI Urge urinary incontinence

MUI Mixed urinary incontinence

OR Odds ratio

CI Confidential interval

IR Insulin resistance

METS Metabolic syndrome

PIR Income-to-Poverty Ratio

OAB Overactive bladder

Acknowledgements

We are grateful to the National Health and Nutrition Examination Survey for the data provided and to all participants for their selfless dedication.

Authors’ contributions

JHL and RJX designed the research. JHL, DW, and MMS collected, analyzed the data and drafted the manuscript. HT, WBG, and JKY revised the manuscript. All authors read and approved the final manuscript.

Funding

This study was supported in part by grants from the Natural Science Foundation of Guangdong Province (2020A1515010541).

Availability of data and materials

No datasets were generated or analysed during the current study.

Declarations

Ethics approval and consent to participate

The portions of this study involving human participants, human materials, or human data were conducted in accordance with the Declaration of Helsinki and were approved by the NCHS Ethics Review Board. The patients/participants provided their written informed consent to participate in this study.

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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