Background and Aims: Accurate diagnosis and treatment of subclinical hypothyroidism (SCH) is challenging in clinical practice because of differing upper limits of normal (ULN) for thyroid-stimulating hormone (TSH). This review summarises the various definitions of SCH and their impact on reported SCH prevalence. Methodology: Articles reporting the prevalence of SCH in relation to the ULN of TSH in human studies were identified through an English-language PubMed search for 'subclinical hypothyroidism,' 'prevalence,' and 'TSH' within the title and/or abstract. Relevant articles and related literature were selected for inclusion. Results: Estimates for the prevalence of SCH varied by sex, age, race/ethnicity, and geographic location (range, 0.4-16.9%). Higher rates of SCH were consistently reported in women (0.9-16.9%) and older individuals (2.7-16.9%). However, the ULN of TSH in those considered free of thyroid disease and not at risk increased progressively with age, suggesting that reports of SCH prevalence in elderly people may be overestimated. Multiple studies reported an increased risk of progression to overt hypothyroidism among individuals with elevated TSH and antithyroid antibodies. Conclusions: Given the variable definition of SCH based on an inconsistent ULN for TSH, it is currently difficult to ascertain the true prevalence of SCH and to correctly label and treat patients with SCH; use of age-adjusted definitions may be considered when assessing prevalence. A diagnosis of SCH does not necessarily merit treatment, especially if TSH elevations are transient (i.e. not persistent for > 3-6 months) and the patient lacks other risk factors for developing overt hypothyroidism.
Review criteriaStudies were identified through a PubMed search for 'subclinical hypothyroidism' (SCH), 'prevalence,' and 'TSH' (thyroid-stimulating hormone) within the title and/or abstract field. The results were limited to English-language studies in humans. Abstracts were reviewed, and studies reporting the prevalence of SCH in relation to the upper limit of normal for TSH were selected for inclusion, as well as additional relevant articles.
Message for the clinicThe true prevalence of SCH is currently difficult to precisely assess, as the current definition of SCH has not been consistently applied in previous studies and does not account for individual patient factors, including the age-adjusted upper limit of normal for TSH, positivity for thyroid antibodies, and racial and ethnic differences. A diagnosis of SCH does not necessarily mean that treatment is merited.