原文 | English |
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頁(從 - 到) | e773-e775 |
期刊 | Journal of the European Academy of Dermatology and Venereology |
卷 | 37 |
發行號 | 6 |
DOIs | |
出版狀態 | Published - 6月 2023 |
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於: Journal of the European Academy of Dermatology and Venereology, 卷 37, 編號 6, 06.2023, p. e773-e775.
研究成果: Letter › 同行評審
TY - JOUR
T1 - Lack of association between vitiligo and major adverse cardiovascular events
T2 - A population-based cohort study
AU - Wu, Po Chien
AU - Ma, Sheng Hsiang
AU - Wu, Chun Ying
AU - Pan, Tzu Yun
AU - Chang, Yun Ting
AU - Wu, Chen Yi
N1 - Funding Information: This study was funded by grants from the Ministry of Science and Technology, Taiwan, R.O.C. (MOST 108-2314-B-075-041-MY3) and Taipei Veterans General Hospital (V111C-022). Vitiligo is a common skin depigmentation disorder drawing disturbances in quality of life and psychological concerns.1 Several mechanisms have been postulated for the development of vitiligo, including T cell-mediated inflammation, oxidative stress impairment and generation of pro-inflammatory cytokines, which may be associated with the risk of major adverse cardiovascular events (MACE).2,3 Studies have explored the relationship between MACE and other skin inflammatory conditions such as psoriasis, atopic dermatitis and alopecia areata,4–6 but the association between vitiligo and MACE remains obscure. Therefore, we conducted this population-based cohort study to investigate this issue. Based on Taiwan's National Health Insurance Research Database between 2007 and 2018, this study was performed in accordance with the Declaration of Helsinki and approved by the National Health Research Institute and the Institutional Review Board of Taipei Veterans General Hospital, Taipei, Taiwan (IRB:2020-06-016BC). All patients diagnosed with vitiligo (ICD-9-CM code 709.01; ICD-10-CM code L80) more than three times in an outpatient department or once in hospitalization by dermatologists were eligible for inclusion. We identified MACE with diagnostic codes of cardiovascular events, including acute myocardial infarction and ischemic heart disease, and cerebrovascular events, including ischemic stroke and haemorrhagic stroke. Certain factors such as age, sex and comorbidities used in propensity-score matching were considered as potential confounders. Comorbidities included hypertension, diabetes mellitus, hyperlipidaemia, renal disease, chronic liver disease, cirrhosis, chronic obstructive pulmonary disease, psychiatric diseases including schizophrenia, autoimmune connective tissue disease and autoimmune thyroid disease and cancer. Other possible risk factors for MACE, such as number of hospital visits, income, phototherapy and vitiligo medications were also analysed. The cumulative incidence and Cox proportional hazards models were used to investigate the risk of MACE. A total of 19,643 patients with vitiligo and 78,572 matched controls were enrolled. Figure 1 presents the cumulative incidence rate of MACE, which showed no significant difference between the vitiligo and non-vitiligo cohorts in 5 years (2.75%; 95% confidence interval [CI], 2.49–3.01 for vitiligo vs. 2.41%; 95% CI, 2.29–2.53 for control, p = 0.08). Table 1 presents the risk factors associated with MACE during the 5-year follow-up period. After adjusting for age, sex, number of hospital visits, income and comorbidities, the association between vitiligo and MACE revealed no significant difference (HR, 1.05; 95% CI, 0.94–1.17; p = 0.37). No significant differences were found between vitiligo and MACE in patients with different subgroups. Abbreviations: CI, confidence interval; HR, hazard ratio; MACE, major adverse cardiovascular events. Adjusted for age, sex, hospital visit number, income, hypertension, diabetes mellitus, hyperlipidaemia, renal disease, chronic liver disease and cirrhosis, chronic obstructive pulmonary disease, psychiatric diseases including schizophrenia, autoimmune connective tissue disease, autoimmune thyroid disease and cancer. To our knowledge, this is the first study to include a large cohort of Asian patients with vitiligo to assess the risk of MACE. Vitiligo has a controversial relationship with cardiovascular risk factors. Greater risks of developing atherosclerosis, metabolic syndrome, dyslipidaemia and myocardial infarction were observed.3,7,8 On the contrary, other evidence found a better lipid profile among vitiligo patients than controls.2,9 There were no consistent findings about the association between vitiligo and cardiovascular risk factors. In addition, a causal relationship required a dose–response effect and plausible pathogenesis, which was not provided in previous literature. Multiple comorbidities, such as hypertension, diabetes mellitus and hyperlipidaemia,10 are well-known risk factors for MACE. To scrutinize the exact effect of vitiligo on the following MACE, we chose the control group by propensity score-matched comorbidities, which was a major advantage over former case–control studies. We provided solid epidemiological evidence for the lack of association between vitiligo and MACE. Limitations of this study included misclassification bias, uncontrolled comorbidities of vitiligo and MACE, and the concern of external validity in non-Asian ethnicities. In conclusion, our study suggests no significant association between vitiligo and the risk of MACE. No significant differences were found between vitiligo and MACE in patients with different age groups, sex and multiple comorbidities. Funding Information: This study was funded by grants from the Ministry of Science and Technology, Taiwan, R.O.C. (MOST 108‐2314‐B‐075‐041‐MY3) and Taipei Veterans General Hospital (V111C‐022).
PY - 2023/6
Y1 - 2023/6
UR - http://www.scopus.com/inward/record.url?scp=85147990711&partnerID=8YFLogxK
U2 - 10.1111/jdv.18936
DO - 10.1111/jdv.18936
M3 - Letter
C2 - 36734285
AN - SCOPUS:85147990711
SN - 0926-9959
VL - 37
SP - e773-e775
JO - Journal of the European Academy of Dermatology and Venereology
JF - Journal of the European Academy of Dermatology and Venereology
IS - 6
ER -