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Postpartum Autoimmune Thyroid Syndrome

机译:产后自身免疫甲状腺综合征

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References(55) Cited-By(26) Postpartum thyroid dysfunction is rather a common problem during postpartum period, found in approximately 5% of mothers in the general population. It occurs from subclinical autoimmune thyroiditis that is aggravated after parturition and causes various types of thyroid dysfunction. Immune activity is physiologically suppressed during pregnancy so that the fetus is not rejected, and rebounds above the normal level after parturition. Graves' disease and Hashimoto's thyroiditis spontaneously ameliorate during pregnancy, and are often aggravated after parturition. The high-risk mothers for postpartum thyroid dysfunction can be well screened by anti-thyroid microsomal antibody (MCAb) and 60% to 70% of MCAb-positive mothers develop postpartum thyroid dysfunction, which is transient in most cases. New onset of Graves' disease may be screened by thyroid stimulating antibody (TSAb) and 70% of TSAb-positive mothers develop either transient or persistent postpartum Graves' disease that usually occurs at 3-6 months postpartum. Immune rebound after parturition may not cause only autoimmune thyroid diseases but other autoimmune Table 4. Various types of postpartum autoimmune disease diseases, which may be investigated with the similar strategies to those in postpartum autoimmune thyroid disease. Thus, we found that postpartum onset of rheumatoid arthritis occured in 0.08% of women in the general population and could be partially predicted by measuring rheumatoid factors in early pregnancy. There are several case reports of other autoimmune diseases developed after delivery; postpartum renal failure or post-delivery hemolyticuremic syndrome, postpartum idiopathic polymyositls, postpartum syndrome with antiphospholipid antibodies, postpartum autoimmune myocarditis. Many other possible postpartum autoimmune diseases are still unexplored. Postpartum autoimmune thyroid syndrome is a good model for understanding the mechanism of onset and aggravation of other autoimmune diseases. Prediction and prevention of postpartum onset of many autoimmune diseases could be established in the near future.
机译:参考文献(55)引用(26)产后甲状腺功能异常在产后时期是一个普遍的问题,在普通人群中约有5%的母亲发现。它由分娩后加重的亚临床自身免疫性甲状腺炎引起,并引起各种类型的甲状腺功能障碍。在怀孕期间,免疫活动在生理上受到抑制,因此胎儿不会被拒绝,并且在分娩后会反弹到正常水平之上。怀孕期间,格雷夫斯氏病和桥本氏甲状腺炎会自发缓解,分娩后通常会加重病情。可以通过抗甲状腺微粒体抗体(MCAb)很好地筛查产后甲状腺功能异常的高危母亲,并且60%至70%的MCAb阳性母亲会发生产后甲状腺功能异常,在大多数情况下是短暂的。可以通过甲状腺刺激抗体(TSAb)来筛查新的Graves病发作,并且70%的TSAb阳性母亲会发展出暂时性或持续性的产后Graves病,通常发生在产后3-6个月。分娩后的免疫反弹可能不仅会导致自身免疫性甲状腺疾病,还会导致其他自身免疫性。表4.各种类型的产后自身免疫性疾病,可以采用与产后自身免疫性甲状腺疾病相似的策略进行研究。因此,我们发现一般人群中有0.08%的女性发生了类风湿关节炎的产后发作,并且可以通过测量妊娠早期的类风湿因子来部分预测。分娩后还有其他一些自身免疫性疾病的病例报告。产后肾衰竭或产后溶血尿毒症综合征,产后特发性多肌炎,具有抗磷脂抗体的产后综合征,产后自身免疫性心肌炎。许多其他可能的产后自身免疫性疾病仍未开发。产后自身免疫性甲状腺综合征是了解其他自身免疫性疾病发病和加重机制的良好模型。在不久的将来,可以建立许多自身免疫性疾病的预测和预防方法。

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