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Thyroid autoimmunity and obstetric outcomes in women with recurrent miscarriage: a case–control study
Kusum Lata1,
Pinaki Dutta2,
Subbiah Sridhar2,
Minakshi Rohilla1,
Anand Srinivasan3,
G R V Prashad1,
Viral N Shah2 and
Anil Bhansali2?
+ Author Affiliations
1Departments of Obstetrics and Gynecology
2Endocrinology
3Pharmacology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India
Correspondence should be addressed to A Bhansali Email: anilbhansaliendocrine@rediffmail.com
Abstract
Objectives Thyroid antibody positivity during pregnancy has been associated with adverse outcomes including miscarriage and preterm delivery. The aim of the study is to evaluate the obstetric outcome in pregnant women with recurrent miscarriage and their response to levothyroxine (l-T4) therapy.
Study design and methods All pregnant and non-pregnant women between 21 and 35 years of age with a history of two or more consecutive miscarriages were included in the study. A third group comprising 100 pregnant women without a history of miscarriage were taken as healthy controls. Thyroid autoimmunity, prevalence of subclinical hypothyroidism and maternal and foetal complications were analysed in all the groups with appropriate statistical methods.
Results The mean age of the patients included in the study was 27.0±3.1 years. Of 100 pregnant patients with previous recurrent miscarriage, thyroid autoimmunity (thyroid peroxidase antibody (TPOAb+) >34?U/ml) was found in 31% of the cases. The incidence of subclinical hypothyroidism was higher in TPOAb+ group than in TPOAb- group (52 vs 16%; P=0.0002). There was no difference in the prevalence of miscarriage or obstetric outcomes between recurrent miscarriage and healthy pregnant women group irrespective of TPO status.
Conclusions The prevalence of thyroid autoimmunity was higher in pregnant women with a history of recurrent abortion compared with healthy pregnant control population. Following l-T4 treatment, there was no difference in prevalence of miscarriage between hypothyroid and euthyroid individuals in TPOAb+ women.
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