Ezzedine Khaled, Soliman Ahmed M, Li Chao, Camp Heidi S, Pandya Amit G
Department of Dermatology, AP-HP, Henri Mondor University Hospital, UPEC, 51 Avenue de Lattre de Tassignv, 94000, Créteil, France.
EA 7379 EpiDermE, Université Paris-Est Créteil (UPEC), Créteil, France.
Dermatol Ther (Heidelb). 2023 Oct;13(10):2265-2277. doi: 10.1007/s13555-023-01001-2. Epub 2023 Sep 5.
Vitiligo is often associated with comorbid conditions that may increase economic burden and affect patients' health-related quality of life. No large-scale study has been published to date using claims databases to evaluate the burden of comorbidities among patients with vitiligo. Herein, we evaluate the comorbidity burden among patients diagnosed with vitiligo from the US.
This retrospective cohort analysis used the Merative MarketScan Commercial Database. Eligible patients were diagnosed with vitiligo between January 2008 and December 2020 and matched 1:4 (vitiligo:control) with control subjects with no diagnosis of vitiligo between January 2007 and December 2021. Study outcomes were the incidence of comorbidities after matching, adjusted hazard ratios of comorbidity incidence among patients with vitiligo relative to matched control subjects, and time to comorbidity diagnosis or incidence.
Baseline demographics were well balanced between matched vitiligo (n = 13,687) and control cohorts (n = 54,748). Incidence rates of comorbidities were higher among patients compared with control subjects (psychiatric, 28.4% vs 22.8%; autoimmune, 13.4% vs 5.1%; and non-autoimmune, 10.0% vs 7.0%). The most common psychiatric and autoimmune comorbidities in patients with vitiligo compared with control subjects included anxiety (14.3% vs 11.0%, respectively), sleep disturbance (9.1% vs 7.1%), depression (8.0% vs 6.3%), atopic dermatitis (3.1% vs 1.1%), psoriasis (2.7% vs 0.6%), and linear morphea (1.5% vs 0.1%). The risk of developing any psychiatric (hazard ratio 1.31; P < 0.01), autoimmune (hazard ratio 2.77; P < 0.01), or non-autoimmune (hazard ratio 1.45; P < 0.01) comorbidity was significantly higher among patients with vitiligo. Time to diagnosis of most vitiligo comorbidities was 1-3 years, although linear morphea was diagnosed at < 1 year.
Results of this retrospective analysis demonstrated that patients were much more likely to be diagnosed with autoimmune or psychiatric comorbidities following a vitiligo diagnosis, which likely contributed to increased economic burden and lower quality of life.
白癜风常与合并症相关,这些合并症可能增加经济负担并影响患者的健康相关生活质量。迄今为止,尚未发表使用索赔数据库评估白癜风患者合并症负担的大规模研究。在此,我们评估了来自美国的白癜风确诊患者的合并症负担。
这项回顾性队列分析使用了默克多市场扫描商业数据库。符合条件的患者在2008年1月至2020年12月期间被诊断为白癜风,并与2007年1月至2021年12月期间未诊断为白癜风的对照受试者按1:4(白癜风:对照)进行匹配。研究结果包括匹配后合并症的发病率、白癜风患者相对于匹配对照受试者的合并症发病率调整后风险比,以及合并症诊断或发病时间。
匹配的白癜风队列(n = 13,687)和对照队列(n = 54,748)之间的基线人口统计学特征平衡良好。患者的合并症发病率高于对照受试者(精神疾病,28.4%对22.8%;自身免疫性疾病,13.4%对5.1%;非自身免疫性疾病,10.0%对7.0%)。与对照受试者相比,白癜风患者最常见的精神疾病和自身免疫性合并症包括焦虑(分别为14.3%对11.0%)、睡眠障碍(9.1%对7.1%)、抑郁症(8.0%对6.3%)、特应性皮炎(3.1%对1.1%)、银屑病(2.7%对0.6%)和线状硬皮病(1.5%对0.1%)。白癜风患者发生任何精神疾病(风险比1.31;P < 0.01)、自身免疫性疾病(风险比2.77;P < 0.01)或非自身免疫性疾病(风险比1.45;P < 0.01)合并症的风险显著更高。大多数白癜风合并症的诊断时间为1至3年,尽管线状硬皮病的诊断时间<1年。
这项回顾性分析的结果表明,白癜风诊断后患者更有可能被诊断出患有自身免疫性或精神疾病合并症,这可能导致经济负担增加和生活质量下降。