Ezzedine Khaled, Diallo Abou, Léauté-Labrèze Christine, Seneschal Julien, Mossalayi Djavad, AlGhamdi Khalid, Prey Sorilla, Bouchtnei Serge, Cario-André Muriel, Boralevi Franck, Jouary Thomas, Taieb Alain
Department of Dermatology and National Reference Centre for Rare Skin Disorders, CHU St-André, 1, rue Jean Burguet 33075 Bordeaux, France.
Arch Dermatol. 2012 Apr;148(4):497-502. doi: 10.1001/archdermatol.2011.351.
To compare factors associated with halo nevi with nonsegmental vitiligo (NSV) vs NSV alone.
Prospective observational study in 553 patients with a confirmed diagnosis of NSV attending a vitiligo clinic between January 1, 2006, and July 1, 2010.
Vitiligo Clinic at the Department of Dermatology, University Hospital Center of Bordeaux, Bordeaux, France.
The Vitiligo European Task Force questionnaire was informed for each patient attending the clinic with a confirmed diagnosis of NSV after the exclusion of other forms of vitiligo (focal, mucosal, and not classifiable). Thyroid function and antithyroid antibodies were screened if not obtained in the previous year.
Extent of disease and markers of autoimmunity or autoinflammation.
Of the 553 patients, 130 had halo nevi-NSV and 423 had NSV. Family history of premature hair graying (odds ratio, 1.74; P < .01) was positively associated with halo nevi-NSV by univariate analysis. Using multivariate analysis, age at onset younger than 18 years, phototype, total body area, localization on the trunk, involvement of hands and feet, and total staging were found to be independent factors. Age at onset younger than 18 years; phototypes I, II, and III; trunk involvement; and staging were positively associated with halo nevi-NSV, whereas this association was negative for total affected area and involvement of hands and feet.
Halo nevi association in NSV affects age at onset and depigmentation pattern and has a stronger link with familial premature hair graying, suggesting that premature hair graying may involve, at least partly, an autoimmune pathway.
比较与晕痣合并非节段性白癜风(NSV)相关的因素与仅患NSV的因素。
对2006年1月1日至2010年7月1日期间在一家白癜风诊所确诊为NSV的553例患者进行前瞻性观察研究。
法国波尔多大学医院中心皮肤科白癜风诊所。
在排除其他形式的白癜风(局限性、黏膜性和不可分类性)后,对诊所中每例确诊为NSV的患者填写白癜风欧洲工作组问卷。如果上一年未检测,则筛查甲状腺功能和抗甲状腺抗体。
疾病范围以及自身免疫或自身炎症标志物。
553例患者中,130例有晕痣合并NSV,423例仅有NSV。单因素分析显示,早生白发家族史(比值比,1.74;P <.01)与晕痣合并NSV呈正相关。多因素分析发现,发病年龄小于18岁、光型、全身面积、躯干部位、手足受累情况和总体分期是独立因素。发病年龄小于18岁;光型I、II和III;躯干受累;以及分期与晕痣合并NSV呈正相关,而与总受累面积和手足受累情况呈负相关。
NSV中的晕痣关联影响发病年龄和色素脱失模式,且与家族性早生白发有更强的联系,提示早生白发可能至少部分涉及自身免疫途径。