Wang Victoria, Walsh Jessica, Zell JoAnn, Verrilli Lauren E, Letourneau Joseph, Johnstone Erica B, Allen-Brady Kristina, Welt Corrine K
Division of Endocrinology, Metabolism and Diabetes, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT 84112.
Division of Rheumatology, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT 84112 USA.
J Clin Endocrinol Metab. 2024 Nov 28. doi: 10.1210/clinem/dgae828.
Autoimmune disease is common in women with primary ovarian insufficiency (POI) and the genetic etiology of autoimmune disease suggests that it could be hereditary in families of women with POI.
We hypothesized that a subset of women with POI and their family members would have increased risk for autoimmune disorders.
Population-based study using electronic health records from 1995-2022.
Two major Utah healthcare systems serving 85% of the state.
Women with POI (n=610) were identified using ICD codes and chart reviewed for accuracy. First-, second-, and third-degree relatives were identified using genealogy data in the Utah Population Database.
Autoimmune diagnoses were identified using ICD codes.
The relative risk of autoimmune disease in women with POI and relatives was estimated by comparison to population rates.
At least one autoimmune disease was identified in 25% of women with POI. The relative risk of autoimmune hypothyroidism (OR [95%CI] 6.88 [5.71, 8.22]; p<0.001), adrenal insufficiency (4.72 [1.73, 10.28]; p=0.0020), type 1 diabetes (4.13 [2.14, 7.22]; p=5.25X10-5), rheumatoid arthritis (5.66 [3.10, 9.50]; p=3.70X10-7), vitiligo (15.33 [6.16, 31.58]; p=5.25X10-7), celiac disease (7.58 [3.47, 14.39]; p=4.47X10-6), psoriasis (3.90 [2.01, 6.81]; p=9.04X10-5) and systemic lupus erythematosus (4.43 [1.63, 9.64]; p=0.0027) were increased in women with POI compared to population rates. There was no increased risk of autoimmune disease in family members.
Data confirm increased autoimmune disease in women with POI. The increased risk is largely related to autoimmune polyglandular syndrome types 1 through 4 and autoimmune hypothyroidism. The absence of risk in family members may result from differences in environmental influences or hormone milieu.
自身免疫性疾病在原发性卵巢功能不全(POI)女性中很常见,自身免疫性疾病的遗传病因表明,在POI女性家族中可能具有遗传性。
我们假设一部分POI女性及其家庭成员患自身免疫性疾病的风险会增加。
基于人群的研究,使用1995 - 2022年的电子健康记录。
犹他州两个主要的医疗保健系统,覆盖该州85%的人口。
使用国际疾病分类(ICD)编码识别POI女性(n = 610),并对病历进行准确性审查。利用犹他州人口数据库中的家谱数据识别一级、二级和三级亲属。
使用ICD编码识别自身免疫性诊断。
通过与总体发病率比较,估计POI女性及其亲属患自身免疫性疾病的相对风险。
25%的POI女性被诊断出至少患有一种自身免疫性疾病。与总体发病率相比,POI女性患自身免疫性甲状腺功能减退症(OR [95%CI] 6.88 [5.71, 8.22];p < 0.001)、肾上腺功能不全(4.72 [1.73, 10.28];p = 0.0020)、1型糖尿病(4.13 [2.14, 7.22];p = 5.25×10⁻⁵)、类风湿性关节炎(5.66 [3.10, 9.50];p = 3.70×10⁻⁷)、白癜风(15.33 [6.16, 31.58];p = 5.25×10⁻⁷)、乳糜泻(7.58 [3.47, 14.39];p = 4.47×10⁻⁶)、银屑病(3.90 [2.01, 6.81];p = 9.04×10⁻⁵)和系统性红斑狼疮(4.43 [1.63, 9.64];p = 0.0027)的相对风险增加。家庭成员患自身免疫性疾病的风险没有增加。
数据证实POI女性患自身免疫性疾病的几率增加。风险增加主要与1型至4型自身免疫性多腺体综合征和自身免疫性甲状腺功能减退症有关。家庭成员没有风险可能是由于环境影响或激素环境的差异。