Vogt Elinor Chelsom, Real Francisco Gómez, Husebye Eystein Sverre, Björnsdottir Sigridur, Benediktsdottir Bryndis, Bertelsen Randi Jacobsen, Demoly Pascal, Franklin Karl Anders, de Aja Gallastegui Leire Sainz, González Francisco Javier Callejas, Heinrich Joachim, Holm Mathias, Jogi Nils Oscar, Leynaert Benedicte, Lindberg Eva, Malinovschi Andrei, Martínez-Moratalla Jesús, Mayoral Raúl Godoy, Oudin Anna, Pereira-Vega Antonio, Semjen Chantal Raherison, Schlünssen Vivi, Triebner Kai, Øksnes Marianne
Department of Clinical Science, University of Bergen, Bergen, Norway.
K.G. Jebsen Center for Autoimmune Disorders, University of Bergen, Bergen, Norway.
Endocr Connect. 2022 May 25;11(5):e220024. doi: 10.1530/EC-22-0024.
To investigate markers of premature menopause (<40 years) and specifically the prevalence of autoimmune primary ovarian insufficiency (POI) in European women.
Postmenopausal women were categorized according to age at menopause and self-reported reason for menopause in a cross-sectional analysis of 6870 women.
Variables associated with the timing of menopause and hormone measurements of 17β-estradiol and follicle-stimulating hormone were explored using multivariable logistic regression analysis. Specific immunoprecipitating assays of steroidogenic autoantibodies against 21-hydroxylase (21-OH), side-chain cleavage enzyme (anti-SCC) and 17alpha-hydroxylase (17 OH), as well as NACHT leucine-rich-repeat protein 5 were used to identify women with likely autoimmune POI.
Premature menopause was identified in 2.8% of women, and these women had higher frequencies of nulliparity (37.4% vs 19.7%), obesity (28.7% vs 21.4%), osteoporosis (17.1% vs 11.6%), hormone replacement therapy (59.1% vs 36.9%) and never smokers (60.1% vs 50.9%) (P < 0.05), compared to women with menopause ≥40 years. Iatrogenic causes were found in 91 (47%) and non-ovarian causes in 27 (14%) women, while 77 (39%) women were classified as POI of unknown cause, resulting in a 1.1% prevalence of idiopathic POI. After adjustments nulliparity was the only variable significantly associated with POI (odds ratio 2.46; 95% CI 1.63-3.42). Based on the presence of autoantibodies against 21 OH and SCC, 4.5% of POI cases were of likely autoimmune origin.
Idiopathic POI affects 1.1% of all women and almost half of the women with premature menopause. Autoimmunity explains 4.5% of these cases judged by positive steroidogenic autoantibodies.
调查欧洲女性中过早绝经(<40岁)的标志物,特别是自身免疫性原发性卵巢功能不全(POI)的患病率。
在对6870名女性的横断面分析中,根据绝经年龄和自我报告的绝经原因对绝经后女性进行分类。
使用多变量逻辑回归分析探讨与绝经时间以及17β-雌二醇和促卵泡激素的激素测量相关的变量。采用针对21-羟化酶(21-OH)、侧链裂解酶(抗SCC)和17α-羟化酶(17 OH)的类固醇生成自身抗体的特异性免疫沉淀测定,以及NACHT富含亮氨酸重复蛋白5来识别可能患有自身免疫性POI的女性。
2.8%的女性被确定为过早绝经,与40岁及以上绝经的女性相比,这些女性未生育(37.4%对19.7%)、肥胖(28.7%对21.4%)、骨质疏松(17.1%对11.6%)、激素替代治疗(59.1%对36.9%)和从不吸烟(60.1%对50.9%)的频率更高(P<0.05)。91名(47%)女性为医源性原因,27名(14%)女性为非卵巢原因,而77名(39%)女性被归类为病因不明的POI,特发性POI的患病率为1.1%。调整后,未生育是唯一与POI显著相关的变量(优势比2.46;95%可信区间1.63 - 3.42)。基于抗21 OH和SCC自身抗体的存在,4.5%的POI病例可能源于自身免疫。
特发性POI影响所有女性的1.1%以及几乎一半的过早绝经女性。通过类固醇生成自身抗体阳性判断,自身免疫解释了这些病例中的4.5%。