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[重症肌无力——性别因素与计划生育]

[Myasthenia gravis-Gender aspects and family planning].

作者信息

Hoffmann Sarah, Verlohren Stefan, Herdick Meret

机构信息

Department of Neurology, Neuroscience Clinical Research Center (NCRC) and Integrated Myasthenia Gravis Center, Charité - Universitätsmedizin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Charitéplatz 1, 10117, Berlin, Deutschland.

Department of Obstetrics, Charité - Universitätsmedizin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Deutschland.

出版信息

Nervenarzt. 2024 Apr;95(4):316-328. doi: 10.1007/s00115-024-01640-6. Epub 2024 Mar 18.

DOI:10.1007/s00115-024-01640-6
PMID:38499774
Abstract

BACKGROUND

There is evidence that gender-specific differences can influence the diagnostics, treatment and long-term disease course of myasthenia gravis (MG). In women the diagnosis is often made during childbearing age.

OBJECTIVE

Gender-specific differences in MG and relevant aspects in routine clinical practice are presented. In addition, current studies on family planning, pregnancy and childbirth in MG are highlighted and treatment recommendations are derived.

MATERIAL AND METHODS

Narrative literature review.

RESULTS

In addition to sociodemographic data, gender-specific differences encompass clinical as well as paraclinical factors, such as disease severity and antibody status. With few exceptions pregnancy is possible with good maternal and neonatal outcome. During pregnancy and peripartum, children of MG patients should be closely monitored for early detection and treatment of potential syndromes caused by diaplacental transfer of maternal antibodies.

CONCLUSION

Gender-specific factors can influence the course of MG. Adequate medical counselling and multidisciplinary collaboration are essential for MG patients who wish to have children.

摘要

背景

有证据表明,性别差异会影响重症肌无力(MG)的诊断、治疗及疾病的长期病程。女性的诊断通常在育龄期作出。

目的

阐述MG中的性别差异及常规临床实践中的相关方面。此外,重点介绍目前关于MG患者计划生育、妊娠及分娩的研究,并得出治疗建议。

材料与方法

叙述性文献综述。

结果

除社会人口统计学数据外,性别差异还包括临床及辅助临床因素,如疾病严重程度和抗体状态。除少数例外情况,妊娠是可行的,母婴结局良好。在妊娠及围产期,应密切监测MG患者的子女,以便早期发现和治疗由母体抗体经胎盘转移引起的潜在综合征。

结论

性别因素可影响MG的病程。对于希望生育的MG患者,充分的医学咨询和多学科协作至关重要。

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1
[Myasthenia gravis-Gender aspects and family planning].[重症肌无力——性别因素与计划生育]
Nervenarzt. 2024 Apr;95(4):316-328. doi: 10.1007/s00115-024-01640-6. Epub 2024 Mar 18.
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本文引用的文献

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Maternal immunoglobulin treatment can reduce severity of fetal acetylcholine receptor antibody-associated disorders (FARAD).母体免疫球蛋白治疗可降低胎儿乙酰胆碱受体抗体相关疾病(FARAD)的严重程度。
Neurol Res Pract. 2023 Oct 26;5(1):58. doi: 10.1186/s42466-023-00280-6.
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Pregnancy outcomes for women with myasthenia gravis and their newborns: A nationwide register-based cohort study.患有重症肌无力的女性及其新生儿的妊娠结局:一项全国范围内基于登记的队列研究。
Eur J Neurol. 2024 Jan;31(1):e16100. doi: 10.1111/ene.16100. Epub 2023 Oct 16.
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Safety and efficacy of zilucoplan in patients with generalised myasthenia gravis (RAISE): a randomised, double-blind, placebo-controlled, phase 3 study.
在全身性重症肌无力患者中zilucoplan 的安全性和疗效(RAISE):一项随机、双盲、安慰剂对照、3 期研究。
Lancet Neurol. 2023 May;22(5):395-406. doi: 10.1016/S1474-4422(23)00080-7.
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Safety and efficacy of rozanolixizumab in patients with generalised myasthenia gravis (MycarinG): a randomised, double-blind, placebo-controlled, adaptive phase 3 study.Rozanolixizumab 在全身性重症肌无力患者中的安全性和疗效(MycarinG):一项随机、双盲、安慰剂对照、适应性 3 期研究。
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The diagnostic and prognostic utility of repetitive nerve stimulation in patients with myasthenia gravis.重复神经刺激在重症肌无力患者中的诊断和预后价值。
Sci Rep. 2023 Feb 20;13(1):2985. doi: 10.1038/s41598-023-30154-5.
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Myasthenia gravis in pregnancy: Systematic review and case series.妊娠合并重症肌无力:系统评价与病例系列
Obstet Med. 2022 Jun;15(2):108-117. doi: 10.1177/1753495X211041899. Epub 2022 Jan 10.
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Independent risk factors for myasthenic crisis and disease exacerbation in a retrospective cohort of myasthenia gravis patients.回顾性重症肌无力患者队列中肌无力危象和疾病恶化的独立危险因素。
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Lancet Neurol. 2022 Feb;21(2):163-175. doi: 10.1016/S1474-4422(21)00357-4.
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Burden of disease in myasthenia gravis: taking the patient's perspective.重症肌无力的疾病负担:从患者角度出发。
J Neurol. 2022 Jun;269(6):3050-3063. doi: 10.1007/s00415-021-10891-1. Epub 2021 Nov 20.