Response to Letter: Are We Really Sure that Subclinical Hypothyroidism and Thyroid Autoimmunity Are Not Associated With Fecundity, Pregnancy Loss, or Live Birth?

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Addressing critiques, this response defends the methodology of a study on subclinical hypothyroidism and fecundity in women with prior pregnancy losses who had not been diagnosed with endometriosis or other gynecologic conditions.

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This response to a letter defends the methodological validity of a study examining subclinical hypothyroidism and thyroid autoimmunity in relation to fecundity and pregnancy loss. The authors argue that relying on patient questionnaires for data collection is necessary because conditions like endometriosis and tubal disease often require invasive procedures or surgery for definitive diagnosis, making clinical visits insufficient proxies. They acknowledge potential limitations regarding undiagnosed endocrinopathies but contend that this approach enhances the generalizability of their findings to a broader population of women with prior pregnancy losses. Relevance to endometriosis: endometriosis is mentioned solely as an exclusion criterion that cannot be easily diagnosed without surgery, highlighting the reliance on self-reported health history rather than serving as a primary subject of investigation.

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We appreciate Paparodis' thoughtful comments regarding our research. Although it is possible that patient self-report can be incorrect, questionnaires can collect personal or risk factor data that often are not included in hospital records. Additionally, questionnaires offer a method for collect data in a standardized fashion (1). Further, although a visit with a gynecologist could rule out current issues (ie, active pelvic inflammatory disease), it would be of little use in diagnosing a prior episode of pelvic inflammatory disease. Many of the disorders we used as exclusion criteria cannot be diagnosed without surgery or an invasive procedure (ie, tubal disease and endometriosis), and a simple visit to the gynecologist is a poor proxy for diagnosis of these disorders. Furthermore, infertility cannot be diagnosed without a careful history, and we must rely on our patients to provide this important information. However, although possible that some women in this population had undiagnosed or unreported endocrinopathy, we believe this actually improves the generalizability of our findings, because they apply to a broader population of women with a history of 1–2 prior losses and have not been diagnosed with these gynecologic conditions. The clinical impact of both thyroid peroxidase (TPO) and thyroglobulin antibodies has been disputed in the literature, and in fact some evidence seems to point to the particular importance of anti-TPO (2, 3). We too were interested in the possible differences in these antibodies and did examine our data based on presence of anti-TPO antibodies vs presence of anti-thyroglobulin antibodies separately and did not observe any differences. However, it is possible that this subanalysis was underpowered; therefore, we combined the antibody positive women into 1 group. In addition, comparison of the mean titer levels between TSH groups yielded similar results. There are certainly some limits to our study, which were noted in our original article. However, to date, this study offers the most insight on the relationship of subclinical hypothyroidism markers and fecundity and early pregnancy loss among a population of generally healthy women with a history of prior losses. We encourage other researchers to further our attempt to address these important clinical questions. Acknowledgments This work was supported by the Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health, Bethesda, MD (Contract Nos. HHSN267200603423, HHSN267200603424, HHSN267200603426). Funding Statement This work was supported by the Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health, Bethesda, MD (Contract Nos. HHSN267200603423, HHSN267200603424, HHSN267200603426). Footnotes - TPO - thyroid peroxidase. References - 1. Saczynski JS, McManus DD, Goldberg RJ. Commonly used data-collection approaches in clinical research. Am J Med. 2013;126(11):946–950. [DOI] [PMC free article] [PubMed] [Google Scholar] - 2. Mehran L, Tohidi M, Sarvghadi F, et al. Management of thyroid peroxidase antibody euthyroid women in pregnancy: comparison of the American Thyroid Association and The Endocrine Society guidelines. J Thyroid Res. 2013;2013:542692. [DOI] [PMC free article] [PubMed] [Google Scholar] - 3. Poppe K, Velkeniers B, Glinoer D. The role of thyroid autoimmunity in fertility and pregnancy. Nat Clin Pract Endocrinol Metab. 2008;4(7):394–405. [DOI] [PubMed] [Google Scholar]

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Autoimmunity Live Birth Female Fertility Humans Hypothyroidism Pregnancy Pregnancy Complications

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