Cited by 174Thyroid Disorders and TreatmentsThyroid and Parathyroid SurgeryThyroid Cancer Diagnosis and Treatment

Subclinical thyroid dysfunction and mortality: an estimate of relative and absolute excess all-cause mortality based on time-to-event data from cohort studies

Haentjens, Patrick, Van Meerhaeghe, Alain, Poppe, Kris, Velkeniers, Brigitte·2008·European Journal of Endocrinology

Abstract

Objectives: To what extent persons with subclinical hyper- or hypothyroidism are more (or less) likely to die than euthyroid control subjects remains a matter of controversy. Methods: We searched electronic reference databases up to July 31, 2007. Three reviewers independently assessed eligibility. Cohort studies published in full that reported data on the hazard ratio (HR) for mortality from all causes in persons with subclinical thyroid dysfunction versus euthyroid controls were included. Results: Based on seven cohorts including 290 participants with subclinical hyperthyroidism, random-effects models estimated that the pooled HR for all-cause mortality was 1.41 (95% confidence interval (CI), 1.12–1.79; P=0.004). Using the pooled HR and standard life-table methods applied to a US reference population, we estimated that a white US woman, when diagnosed with subclinical hyperthyroidism at age of 70, has an excess mortality of 1.5, 4.0, and 8.7% at 2, 5, and 10 years respectively after diagnosis. Likewise, a white US man has an excess mortality of 2.3, 5.7, and 10.7%. For the nine cohorts including 1580 participants with subclinical hypothyroidism, observed heterogeneity (Q test P=0.006; I2=63%) disappeared after pooling cohorts in predefined subgroups according to the presence or absence of a comorbid condition. In doing so, the pooled HR for all-cause mortality was 1.03 (95% CI, 0.78–1.35; P=0.83) in cohorts from the community and 1.76 (95% CI, 1.36–2.30; P<0.001) in cohorts of participants with comorbidities (P=0.014 for heterogeneity among study groups). Conclusions: Individuals with subclinical hyperthyroidism demonstrate a 41% increase in relative mortality from all causes versus euthyroid control subjects. Mathematical modeling suggests that absolute excess mortality after diagnosis might depend on age, with an increase beyond the age of 60, especially in aging men. For patients with subclinical hypothyroidism, the relative risk of all-cause mortality is increased only in patients with comorbid conditions.

Integrity signals

Registry

Crossref · 10.1530/eje-08-0110

Cites

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Cardiovascular morbidity and mortality are particularly increased in men, in elderly patients with high-normal FT4 levels and in patients with underlying heart disease.

    “Cardiovascular morbidity and mortality are particularly increased in men, in elderly patients with high-normal FT 4 levels and in patients with underlying heart disease [71-73, 76, 77, 87, 91, 92, 94] .”
  • Four meta-analyses found an association between subclinical hyperthyroidism and cardiovascular or all-cause mortality, especially in elderly patients and in patients with co-morbidities.

    “Two did not find a link between SHyper and mortality [89,90] , whereas four other meta-analyses found an association between SHyper and cardiovascular or all-cause mortality [71,[91][92][93] , especially in elderly patients and in patients with co-morbidities [91,92] .”
  • Subclinical hyperthyroidism with low but detectable TSH is associated with increased overall mortality in older subjects.

    “Some of these studies re-ported increased risks of overall mortality in older subjects (380,429), cardiovascular events (391), heart failure (381), and atrial fibrillation in all subjects (401) or in older subjects (384), and vertebral fractures in older women (408).”

The citation lists haven’t been fetched yet

References 80 · Cited by 174

Authors
Haentjens, P., Van Meerhaeghe, A., Poppe, K., & Velkeniers, B.
Affiliations
Vrije Universiteit Brussel (BE)
Corresponding author
Haentjens, Patrick
Venue
European Journal of Endocrinology
Published
2008-09
Volume
159
Issue
3
Pages
329-341
ISSN
  • 0804-4643 (ISSN-L)
  • 1479-683X
OpenAlex
W2169217046
Cited by
174
References
80
Citations by year
2025: 4 · 2024: 1 · 2023: 2 · 2022: 3 · 2021: 4 · 2020: 6 · 2019: 9 · 2018: 7 · 2017: 10 · 2016: 7 · 2015: 11 · 2014: 18 · 2013: 15 · 2012: 24
FWCI
12.79
Type
journal article
Language
en
Open access
closed
Locations
  • European Journal of Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
  • VUBIR (Vrije Universiteit Brussel) (submittedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Thyroid Disorders and Treatments
  • Health Sciences › Medicine › Surgery › Thyroid and Parathyroid Surgery
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Thyroid Cancer Diagnosis and Treatment
Keywords
subclinical hyperthyroidism, subclinical hypothyroidism, subclinical thyroid dysfunction, all-cause mortality, excess mortality, comorbidities, pooled hazard ratio, time-to-event data, cohort studies, older men, women's health, mortality prediction, age at diagnosis, sex differences in mortality
MeSH terms
Adult, Aged, Aged, 80 and over, Algorithms, Cause of Death, Female, Humans, Hyperthyroidism, Hypothyroidism, Male, Middle Aged, Thyroid Diseases, Time Factors, Models, Statistical, Cohort Studies, Case-Control Studies, Age of Onset

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review