Psychiatric Comorbidities in Women with Complete Androgen Insensitivity Syndrome or Müllerian Aplasia/Agenesis.

IF 5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Clinical Endocrinology & Metabolism Pub Date : 2024-10-11 DOI:10.1210/clinem/dgae720
Behzad Sorouri Khorashad, Oumaima Kaabi, Melissa D Gardner, Darios Getahun, Michael Goodman, Timothy L Lash, Peter A Lee, Courtney McCracken, Joshua May, Maria Muzik, Suma Vupputuri, Rami Yacoub, David E Sandberg
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Abstract

Context: Understanding mental health issues facing individuals with disorders/differences of sex development (DSD) is crucial for optimizing evidence-based practices in this population.

Objectives: To compare the prevalence of psychiatric diagnoses among patients diagnosed with complete androgen insensitivity syndrome (CAIS) or Müllerian duct aplasia/agenesis (MA) to male and female reference groups.

Design: Retrospective cohort study.

Setting: Three large integrated health systems.

Participants: All individuals with confirmed CAIS or MA enrolled in one of three Kaiser Permanente healthcare systems between January 1, 1988, and January 31, 2017. For each DSD patient, age-, race/ethnicity- and health system-matched male and female referents with typical sex development were randomly selected.

Outcomes/measures: Mental health diagnoses and use of psychiatric medications.

Results: The prevalence of anxiety and depressive disorders in the CAIS and MA cohorts was approximately twice as high as in male referents without DSD, but the corresponding differences relative to female referents were less evident. A subgroup of MA patients with uterine agenesis had higher prevalence of bipolar disorder than either reference group, but these results were accompanied by wide confidence intervals. Women with CAIS and MA more frequently filled psychiatric medications compared to male but not female referents.

Conclusion: On balance, these findings are reassuring, albeit requiring confirmation in other settings. Future studies using longitudinal designs and patient-reported outcomes are needed to evaluate changes in mental health status of CAIS and MA patients at different ages and different intervals following initial diagnosis.

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患有完全雄激素不敏感综合征或缪勒氏腺增生症/先天性缪勒氏腺发育不良的女性的精神并发症。
背景:了解性别发育障碍/差异(DSD)患者面临的心理健康问题对于优化该人群的循证治疗至关重要:目的:比较被诊断为完全雄激素不敏感综合征(CAIS)或穆勒氏管增生/发生(MA)的患者与男性和女性参照组的精神病诊断率:设计:回顾性队列研究:环境:三个大型综合医疗系统:1988年1月1日至2017年1月31日期间在三个凯撒医疗保健系统中的一个系统注册的所有确诊CAIS或MA患者。对于每位DSD患者,随机选取年龄、种族/民族和医疗系统匹配的具有典型性发育的男性和女性参照者:结果/测量:精神健康诊断和精神科药物使用:结果:在 CAIS 和 MA 群体中,焦虑症和抑郁症的发病率约为无 DSD 的男性参照者的两倍,但与女性参照者相比,相应的差异并不明显。子宫无发育的躁狂症患者亚组的躁狂症发病率高于任何一个参照组,但这些结果的置信区间较宽。与男性参照组相比,患有 CAIS 和 MA 的女性更经常服用精神科药物,但女性参照组则没有:总的来说,这些研究结果令人欣慰,尽管还需要在其他环境中得到证实。未来的研究需要采用纵向设计和患者报告结果,以评估CAIS和MA患者在初次诊断后不同年龄段和不同间隔期的心理健康状况变化。
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来源期刊
Journal of Clinical Endocrinology & Metabolism
Journal of Clinical Endocrinology & Metabolism 医学-内分泌学与代谢
CiteScore
11.40
自引率
5.20%
发文量
673
审稿时长
1 months
期刊介绍: The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.
期刊最新文献
Arterial Stiffness Associated with Long-Term Major Adverse Cardiac Events in Patients of Primary Aldosteronism. Dose-specific effects of denosumab on serum calcium levels in patients with osteoporosis and various renal functions. Gestational diabetes: an update sixty years after O'Sullivan and Mahan. Psychiatric Comorbidities in Women with Complete Androgen Insensitivity Syndrome or Müllerian Aplasia/Agenesis. Signs of Potential Androgen Excess Across the Lifespan in a US-based Digital Cohort Study.
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