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女性脆性X前突变:认识到原发性卵巢功能不全之外的健康挑战。

Fragile X premutation in women: recognizing the health challenges beyond primary ovarian insufficiency.

作者信息

Hoyos Luis R, Thakur Mili

机构信息

Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.

Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.

出版信息

J Assist Reprod Genet. 2017 Mar;34(3):315-323. doi: 10.1007/s10815-016-0854-6. Epub 2016 Dec 19.

Abstract

Fragile X premutation carriers have 55-200 CGG repeats in the 5' untranslated region of the FMR1 gene. Women with this premutation face many physical and emotional challenges in their life. Approximately 20% of these women will develop fragile X-associated primary ovarian insufficiency (FXPOI). In addition, they suffer from increased rates of menstrual dysfunction, diminished ovarian reserve, reduction in age of menopause, infertility, dizygotic twinning, and risk of having an offspring with a premutation or full mutation. Consequent chronic hypoestrogenism may result in impaired bone health and increased cardiovascular risk. Neuropsychiatric issues include risk of developing fragile X-associated tremor/ataxia syndrome, neuropathy, musculoskeletal problems, increased prevalence of anxiety, depression, and sleep disturbances independent of the stress of raising an offspring with fragile X syndrome and higher risk of postpartum depression. Some studies have reported a higher prevalence of thyroid abnormalities and hypertension in these women. Reproductive health providers play an important role in the health supervision of women with fragile X premutation. Awareness of these risks and correlation of the various manifestations could help in early diagnosis and coordination of care and services for these women and their families. This paper reviews current evidence regarding the possible conditions that may present in women with premutation-sized repeats beyond FXPOI.

摘要

脆性X前突变携带者在FMR1基因的5'非翻译区有55 - 200个CGG重复序列。携带这种前突变的女性在生活中面临许多身体和情感挑战。这些女性中约20%会发展为脆性X相关原发性卵巢功能不全(FXPOI)。此外,她们还存在月经功能障碍发生率增加、卵巢储备功能下降、绝经年龄提前、不孕、双卵双胎以及生育携带前突变或全突变后代的风险。随之而来的慢性雌激素缺乏可能导致骨骼健康受损和心血管疾病风险增加。神经精神问题包括发展为脆性X相关震颤/共济失调综合征、神经病变、肌肉骨骼问题的风险,焦虑、抑郁和睡眠障碍的患病率增加,这些与抚养患有脆性X综合征的后代所带来的压力无关,且产后抑郁症的风险更高。一些研究报告称这些女性甲状腺异常和高血压的患病率较高。生殖健康提供者在对携带脆性X前突变的女性进行健康监测方面发挥着重要作用。了解这些风险以及各种表现之间的关联有助于对这些女性及其家庭进行早期诊断以及护理和服务的协调。本文综述了关于携带前突变大小重复序列的女性除FXPOI外可能出现的其他病症的现有证据。

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