==== Front J Evid Based Integr MedJ Evid Based Integr MedCHPspchpJournal of Evidence-based Integrative Medicine2515-690XSAGE Publications Sage CA: Los Angeles, CA 10.1177/2515690X1878937410.1177_2515690X18789374Original ArticleInhibitory Effect of Chunghyul-dan on Stroke Recurrence in Small Vessel Disease Patients: A 5-Year Observational Study Jung Woo-Sang MD, PhD1*Min In Kyu MD, PhD1*Jin Chul MD, MS1Park Joo Young MD, MS1Kim Hyung Gyu MD, PhD2Kwak Young MD, PhD3Kim Kyung Wook MD, PhD4Cho Seung-Yeon MD, PhD1Park Seong-Uk MD, PhD1Moon Sang-Kwan MD, PhD1Park Jung-Mi MD, PhD1Ko Chang-Nam MD, PhD1Cho Ki-Ho MD, PhD1http://orcid.org/0000-0002-1857-3515Kwon Seungwon MD, PhD1 1 Department of Cardiology and Neurology, College of Korean Medicine, Kyung Hee University, Seoul, Republic of Korea 2 Se-Bong Korean Medical Clinic, Busan, Republic of Korea 3 In-Soo Korean Medical Clinic, Gyunggi-do, Republic of Korea 4 Seo-Cho Korean Medical Clinic, Seoul, Republic of Korea * Both authors contributed equally to this work as co-first authors.Seungwon Kwon MD, PhD, Department of Cardiology and Neurology, College of Korean Medicine, Kyung Hee University, 23 KyunHee-daero, Dongdaemun-gu, Seoul 02447, Republic of Korea. Email: kkokkottung@hanmail.net26 7 2018 2018 23 2515690X1878937412 2 2018 29 3 2018 26 6 2018 © The Author(s) 20182018SAGE Publications Inc unless otherwise noted. Manuscript content on this site is licensed under Creative Commons LicensesThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).We investigated the stroke recurrence rate and the rate of adverse effects induced by an herbal medicine, Chunghyul-dan, administered to patients over a 5-year period. We prescribed 600 mg Chunghyul-dan a day to patients with small vessel diseases and investigated stroke recurrence, adverse effects, and drug compliance for 5 years. The primary outcome was the prevalence of stroke recurrence (in 3, 4, and 5 years). The secondary outcome was the frequency of adverse effects induced by Chunghyul-dan. We recruited 400 patients. Among them, 270, 233, and 195 patients completed 3, 4, and 5 years of follow-up, respectively. Among patients who completed 3, 4, and 5 years of follow-up, cumulative recurrent stroke occurred in 7 (2.6%), 11 (4.7%), and 12 (6.2%) patients. There were no adverse effects. We suggest that Chunghyul-dan might be useful for the inhibition of stroke recurrence by reducing microangiography progression. Further study is needed to confirm our hypothesis. Chunghyul-danischemic strokesmall vessel diseasesecondary preventionherbal medicineKyung Hee Universityhttps://doi.org/10.13039/501100002597KHU-20120328cover-dateJanuary-December 2018 ==== Body To prevent stroke recurrence, antiplatelet agents have been used worldwide as conventional therapy. However, adverse effects including an increase in hemorrhagic tendency, gastrointestinal disturbance, neutropenia, and purpura are associated with the use of antiplatelet agents.1 Furthermore, the inhibitory effect of antiplatelet agents is not sufficient (8% to 13%).2–8 Therefore, we need another strategy for secondary stroke prevention. Chunghyul-dan is an herbal complex consisting of Scutellariae Radix, Coptidis Rhizoma, Phellodendri Cortex, Gardeniae Fructus, and Rhei Rhizoma. Chunghyul-dan can inhibit 3-hydroxy-3-methylglutaryl (HMG) coenzyme A (CoA) reductase.9 It also has anti-apoptotic,10 anti-oxidative,11 anti-inflammatory,11 antihypertensive,12 and antilipidemic effects.13 We believe that these biochemical effects of Chunghyul-dan reduce the progress of microangiopathy, which is a supposedly major factor in the progression of small vessel disease. Therefore, we propose that Chunghyul-dan has an inhibitory effect on stroke occurrence induced by small vessel disease. Two previous clinical studies led to the confirmation that the administration of Chunghyul-dan for 1 or 2 years inhibits the recurrence of a secondary stroke in silent cerebral infarction patients or small vessel diseases of the brain.14,15 To expand these results, we investigated the stroke recurrence rate and the rate of adverse effects induced by Chunghyul-dan, which was administered to patients over a 5-year period. Methods We recruited study participants with small vessel diseases from January 1, 2001, to December 31, 2009, in the Stroke Center of Kyung Hee University Korean Medicine Hospital, Seoul, Korea. Small vessel disease was diagnosed using the Classification of Cerebrovascular Disease III16 (see the appendix). In addition, cases with potential cardioembolic sources or significant proximal arterial stenosis in brain imaging were excluded. Chunghyul-dan is a capsulated 80% ethanol extract (300 mg per capsule) composed of Scutellariae Radix, Coptidis Rhizoma, Phellodendri Cortex, Gardeniae Fructus, and Rhei Rhizoma (Table 1). Extraction of each herb was performed with 80% ethanol in boiling water for 2 hours. The extracts were filtered and evaporated in a rotary vacuum evaporator and finally lyophilized with a freezing dryer. To standardize the quality of Chunghyul-dan, berberine in Coptidis Rhizoma and Phellodendri Cortex, baicalin in Scutellariae Radix, geniposide in Gardeniae Fructus, and sennoside A in Rhei Rhizoma were quantitatively assayed according to previous methods.17 Table 1. Composition of Chunghyul-dan. Constituent Herbs Binomial Name Weight (g) Scutellariae Radix Scutellaria baicalensis Georgi (from Korea) 0.28 Coptidis Rhizoma Coptis japonica Makino (from Korea) 0.28 Phellodendri Cortex Phellodendron amurense Ruprecht (from Korea) 0.28 Gardenia Fructus Gardenia jasminodes Ellis (from Korea) 0.28 Rhei Rhizoma Rheum palmatum L. (from Korea) 0.07 Total 1.2 The study protocol was as follows (Figure 1). We used an observational cohort study design. Details of concomitant diseases such as previous stroke, hypertension, diabetes mellitus, dyslipidemia, and smoking habits were obtained from all patients at the time of enrollment. The diagnoses of hypertension, diabetes mellitus, and dyslipidemia were assigned to patients already receiving medication or when the World Health Organization diagnostic criteria were fulfilled. Every participant confirmed eligible. Figure 1. Flow chart. We prescribed 600 mg (2 capsules) per day of Chunghyul-dan to the patients and monitored their drug compliance, adverse effects, and stroke recurrence every 2 months for a period of 5 years. Data collection was conducted by a single independent researcher every 2 to 3 months, and the following outcomes were evaluated based on these data. The primary outcome of this study was the prevalence of ischemic stroke recurrence during the follow-up period (36 months, 48 months, and 60 months after consecutive administration of Chunghyul-dan). The secondary outcome was the frequency of adverse effects due to the administration of Chunghyul-dan. Stroke recurrence was defined as the occurrence of a new clinical syndrome—characterized by rapidly developing clinical symptoms and signs of focal and at times global loss of brain function—accompanied by evidence (from a brain imaging) of new cerebral infarction in the clinically relevant area of the brain. If there is the detection of a new lesion of the brain through brain magnetic resonance imaging without neurological symptoms in medical checkup, we also defined it as asymptomatic ischemic stroke recurrence. When a patient completed 5 years of Chunghyul-dan administration and showed lesions with magnetic resonance imaging scan, we performed follow-up brain magnetic resonance imaging to confirm the presence of new lesions by comparing it to the baseline image, which was taken 5 years ago. Results We recruited 400 patients with small vessel diseases of the brain. Among them, 270, 233, and 195 patients completed 3, 4, and 5 years of follow-up, respectively. Chunghyul-dan was administered for 35.5 ± 3.2 months (average ± standard deviation) in 270 subjects who completed 3 years of follow-up. Two hundred thirty-three patients who completed 4 years of follow-up took Chunghyul-dan for 47.0 ± 5.4 months. Furthermore, Chunghyul-dan was administered for 58.1 ± 8.3 months in patients (195 patients) who completed 5 years of follow-up. The other 205 patients did not complete the 5-year follow-up period. We tried to contact them by telephone to assess their prognosis and to investigate the causes of drop out. Information was obtained about 63 patients. Specific causes of drop out are shown in Figure 1. Among the 270 patients who completed the 3-year follow-up, recurrent stroke occurred in 7 patients. The recurrent rate was estimated as 2.6%. From 3 to 4 years of follow-up, recurrent stroke occurred in 4 of 233 patients. The cumulative recurrent rate of 4 years of follow-up was estimated as 4.7%. After 5 years of follow-up, 12 of 195 patients revealed recurrent stroke. Therefore, the cumulative recurrent rate of 5 years was estimated as 6.2%. The survival curve of survival probability without recurrence is shown in Figure 2. Figure 2. Survival curve of survival probability without ischemic stroke recurrence. There were no adverse effects induced by Chunghyul-dan administration. Among the patients, 63.3% to 69.2% were co-administered antiplatelet medications such as aspirin or clopidogrel (Table 2). The specific time information on the 12 patients who revealed stroke recurrence is outlined in Figure 1. Table 2. Patients’ Demographic Data and 5-Year Follow-up Results. 3-Year Follow-up 4-Year Follow-up 5-Year Follow-up Number of patients 270 233 195 Gender (male–female) 137:133 119:114 97:98 Age (years), mean (SD) 66.7 (8.5) 66.9 (8.3) 67.1 (8.5) Concomitant diseases, n (%)  Previous stroke 101 (37.4) 97 (41.6) 90 (46.2)  Hypertension 191 (70.7) 172 (73.8) 147 (75.4)  Diabetes mellitus 82 (30.4) 71 (30.5) 62 (31.8)  Dyslipidemia 79 (29.3) 79 (33.9) 71 (36.4) Current smoker, n, (%) 24 (8.9) 21 (9.0) 15 (7.7) Family history of stroke, n, (%) 82 (30.4) 71 (30.5) 67 (34.4) Use of combined antiplatelet therapy, n, (%) 171 (63.3) 152 (65.2) 135 (69.2)   Aspirin 128 (47.4) 112 (48.1) 101 (51.8)   Clopidogrel 55 (20.4) 48 (20.6) 40 (20.5) Period of CHD administration (months), mean (SD) 35.5 (3.2) 47.0 (5.4) 58.1 (8.3) Cumulative number of stroke recurrence, n, (%) 7 (2.6) 11 (4.7) 12 (6.2) Number of adverse effect, n, (%) 0 0 0 Abbreviation: CHD, Chunghyul-dan. Discussion In the present study, we demonstrated that the 5-year stroke recurrence rate of Chunghyul-dan-treated patients (Chunghyul-dan mono or Chunghyul-dan combined therapy) was 6.2%. There were no adverse effects induced by Chunghyul-dan intake. Although there is no control in this study, to show the superiority of Chunghyul-dan over conventional antiplatelet agents, we suggest historical controls, which used antiplatelet agents for the secondary prevention of stroke (Table 3).2–8 Considering that previous studies reported that the inhibitory rate of aspirin, clopidogrel, dipyridamole, and dual antiplatelet therapies on stroke recurrence was 8.0% to 12.8% during a relatively short period (18-72 months), the recurrence rate of stroke in this study is much lower (6.2%). Although we think that we cannot directly compare the recurrence rate of our study with these studies, we believe that these results indirectly show the superiority of Chunghyul-dan on secondary stroke prevention compared with conventional antiplatelet agents. Chunghyul-dan is safe to use. There were no adverse effects induced by Chunghyul-dan. These results are in accordance with the previous studies.14,15 Table 3. Prevalence of Ischemic Stroke Recurrence in the Historical Controls in the Previous Studies.2–8 Articles Patients Interventions and Follow-up Period Prevalence of Stroke Recurrence, % ESPS Group (1990)2 Previous TIA or stroke Aspirin 75 mg + dipyridamole 330 mg/day for 24 months 9.1 Farrell et al (1991)3 Previous TIA Aspirin 1200 mg/day for 72 months 12.4 Aspirin 300 mg/day for 72 months 12.4 The SALT Collaborative Group (1991)4 Previous TIA or stroke Aspirin 75 mg/day for 32 months 12.1 Diener et al (1996)5 Previous TIA or stroke Aspirin 50 mg/day for 24 months 12.5 Dipyridamole 400 mg/day for 24 months 12.8 Aspirin 50 mg + dipyridamole 400 mg/day for 24 months 9.5 Matia-Guiu et al (2003)8 Previous TIA or stroke Aspirin 325 mg for 30.1 months 9.6 Triflusal 600 mg for 30.1 months 9.7 Diener et al (2004)6 Previous TIA or stroke Clopidogrel 75 mg for 18 months 8.0 Aspirin 75 mg + clopidogrel 75 mg for 18 months 8.0 Shinohara et al (2010)7 Previous ischemic stroke Aspirin 81 mg/day for 29 months 8.9 Cilostazol 100 mg/day for 29 months 6.1 Abbreviation: transient ischemic attack. We assume that the mechanism of the preventive effect of Chunghyul-dan in secondary stroke might be based on various biochemical effects on microangiopathy that are closely related to cell cycle progression, hypertension, dyslipidemia, vascular inflammation, and oxidative damage. Previous clinical studies using Chunghyul-dan showed that it has anti-hypertensive12 and anti-hyperlipidemic effects.13 Previous experimental studies including in vivo and in vitro studies also suggested that Chunghyul-dan inhibits HMG-CoA reductase and pancreatic lipase9 and shows anti-oxidative (by scavenging free radicals) and anti-inflammatory activity.11 Another experimental study also suggested that Chunghyul-dan acts as an anti-apoptotic agent, a cell cycle progressive agent, and a cell-migration–inducing agent.10 In this study, Chunghyul-dan was prescribed at 600 mg (2 capsules) per day. In a previous study that examined the clinical effects of Chunghyul-dan on dyslipidemia, we compared the effects of Chunghyul-dan 600 mg/day with 1200 mg/day.18 There was a statistically significant decrease in total cholesterol after 8 weeks at both 600 mg/day and 1200 mg/day, but no significant difference was observed between 600 mg/day and 1200 mg/day. Based on this result, a 600 mg dose was also used in a study that observed the effect of preventing the recurrence of small vessel disease for 2 years.15 Recently, a study of the prompt effect of Chunghyul-dan on cerebral hemodynamics showed that 600 mg was more effective than 1200 mg, once again supporting the 600 mg dose.19 The limitations of this study are as follows. First, there was no control group because it was not a randomized controlled trial. Due to lack of concurrent control, we suggest historical controls. However, there are also limitations because historical controls were mostly from non-Asian populations. Furthermore, these historical controls did not focus on small vessel diseases and there are some differences in demographic data between the historical control group and the patients. Second, about 65% of the patients used antiplatelet therapy such as aspirin and clopidogrel. Therefore, it cannot be concluded clearly whether the results of the present study were the effects of Chunghyul-dan alone or Chunghyul-dan combination. Finally, during a 5-year follow-up period, the patients showed a 50% high dropout rate and poor drug compliance. Because of these limitations, it is difficult to obtain a concrete conclusion about the effect of Chunghyul-dan to prevent the recurrence of small vessel disease. Conclusions We cannot draw a concrete conclusion from this study because of limitations as mentioned. However, considering that the stroke recurrence rate of subjects to whom Chunghyul-dan was administered was much lower than that of the historical control groups, we suggest that Chunghyul-dan might be useful in the prevention of ischemic stroke recurrence by reducing microangiography progression. Further study is needed to confirm our hypothesis. Author Contributions: Study design, writing, data interpretation (Seungwon Kwon, Woo-Sang Jung, and In Kyu Min), data collection (Chul Jin, Joo Young Park), data review and analysis (Hyung Gyu Kim, Young Kwak, and Kyung Wook Kim), data review and literature search (Seong-Uk Park, Sang-Kwan Moon, Jung-Mi Park, Chang-Nam Ko, and Ki-Ho Cho). Declaration of Conflicting Interests: The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. Funding: The authors received the following financial support for the research, authorship, and/or publication of this article: This work was supported by a grant from the Kyung Hee University in 2012 (KHU-20120328). ORCID iD: Seungwon Kwon, MD, PhD http://orcid.org/0000-0002-1857-3515 Ethical Approval: The Institutional Research Board of Kyung Hee University Korean Medicine Hospital approved this study (KOMCIRB-2011-34). Appendix Criteria for small vessel disease (either condition A, B, or C is true). Condition A Brain images show a deep infarct of 1.5 cm in its maximal diameter that is appropriate to a clinical classical lacunar syndrome. Condition B Brain image shows no lesion to explain the clinical syndrome, and the clinical presentation is one (including the following) classically associated with a small deep infarct: (1) Pure motor hemiplegia: hemiparesis or hemiplegia involving the face, arm and leg equally, or arm and leg equally, without other neurological findings. Although mild sensory symptoms can be present, there is no sensory loss on examination that is related to the infarct. (2) Pure sensory stroke: isolated sensory loss or disturbance involving the entire hemiface and hemibody or the hemibody alone. There may be incidental motor weakness from another cause. (3) Ataxia-hemiparesis: hemiparesis with ipsilateral ataxia. Paresis is more commonly crural. (4) Dysarthria-clumsy hand syndrome: dysarthria with a clumsy hand. Facial weakness is possible. (5) Hemiballismus, hemiathetosis, or hemidystonia; must be of acute onset. (6) Sensorimotor stroke: weakness and sensory loss involving face, arm and leg equally, without other neurological findings. Condition C Computed tomography scan shows a deep infarct of <1.5 cm in its maximal diameter that is appropriate to the clinical syndrome, but the syndrome is not one of the classical syndromes for lacunar stroke. ==== Refs References 1 McCabe DJ Brown MM Prevention of ischaemic stroke—antiplatelets . 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