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Meta-Analysis
. 2021 Dec 1;78(12):1375-1383.
doi: 10.1001/jamapsychiatry.2021.2506.

Association of Hypothyroidism and Clinical Depression: A Systematic Review and Meta-analysis

Henry Bode  1 , Beatrice Ivens  1 , Tom Bschor  2 , Guido Schwarzer  3 , Jonathan Henssler  1   4 , Christopher Baethge  1
Affiliations
Meta-Analysis

Association of Hypothyroidism and Clinical Depression: A Systematic Review and Meta-analysis

Henry Bode et al. JAMA Psychiatry. .

Abstract

Importance: Hypothyroidism is considered a cause of or a strong risk factor for depression, but recent studies provide conflicting evidence regarding the existence and the extent of the association. It is also unclear whether the link is largely due to subsyndromal depression or holds true for clinical depression.

Objective: To estimate the association of hypothyroidism and clinical depression in the general population.

Data sources: PubMed, PsycINFO, and Embase databases were searched from inception until May 2020 for studies on the association of hypothyroidism and clinical depression.

Study selection: Two reviewers independently selected epidemiologic and population-based studies that provided laboratory or International Statistical Classification of Diseases and Related Health Problems diagnoses of hypothyroidism and diagnoses of depression according to operationalized criteria (eg, Diagnostic and Statistical Manual of Mental Disorders or International Statistical Classification of Diseases and Related Health Problems) or cutoffs in established rating scales.

Data extraction and synthesis: Two reviewers independently extracted data and evaluated studies based on the Newcastle-Ottawa Scale. Summary odds ratios (OR) were calculated in random-effects meta-analyses.

Main outcomes and measures: Prespecified coprimary outcomes were the association of clinical depression with either hypothyroidism or autoimmunity.

Results: Of 4350 articles screened, 25 studies were selected for meta-analysis, including 348 014 participants. Hypothyroidism and clinical depression were associated (OR, 1.30 [95% CI, 1.08-1.57]), while the OR for autoimmunity was inconclusive (1.24 [95% CI, 0.89-1.74]). Subgroup analyses revealed a stronger association with overt than with subclinical hypothyroidism, with ORs of 1.77 (95% CI, 1.13-2.77) and 1.13 (95% CI, 1.01-1.28), respectively. Sensitivity analyses resulted in more conservative estimates. In a post hoc analysis, the association was confirmed in female individuals (OR, 1.48 [95% CI, 1.18-1.85]) but not in male individuals (OR, 0.71 [95% CI, 0.40-1.25]).

Conclusions and relevance: In this systematic review and meta-analysis, the effect size for the association between hypothyroidism and clinical depression was considerably lower than previously assumed, and the modest association was possibly restricted to overt hypothyroidism and female individuals. Autoimmunity alone may not be the driving factor in this comorbidity.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Schwarzer reported personal fees from Roche Pharma as external statistical consultant outside the submitted work. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. PRISMA Flow Diagram
Figure 2.
Figure 2.. Association of Hypothyroidism and Depression
OR indicates odds ratio.
Figure 3.
Figure 3.. Association of Thyroid Peroxidase Antibodies Positivity and Depression
OR indicates odds ratio.
See this image and copyright information in PMC

Comment in

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