Evidence map›Paper›PMID 42047117›Full record

SynthesisBiomolecules & biomedicine2026

Metabolic syndrome and incident thyroid cancer risk in adults: A systematic review and meta-analysis.

Zhengwen He, Jing Zhou, Xianxiang Lu

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Biomolecules & biomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Zhengwen HeDepartment of Endocrinology, the Fifth People's Hospital of Zhangjiagang City, Zhangjiagang, China.
Jing ZhouDepartment of Endocrinology, the Fifth People's Hospital of Zhangjiagang City, Zhangjiagang, China.
Xianxiang LuDepartment of Endocrinology, the Fifth People's Hospital of Zhangjiagang City, Zhangjiagang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The global incidence of thyroid cancer (TC) has increased, with metabolic syndrome (MetS) identified as a potential modifiable risk factor. However, epidemiological evidence regarding this association remains inconsistent. We conducted a meta-analysis to quantify the relationship between MetS and the risk of incident TC in adult populations. We searched PubMed, Embase, and Web of Science for longitudinal observational studies assessing MetS in relation to incident TC. Risk ratios (RRs) with 95% confidence intervals (CIs) were pooled using random-effects models to account for heterogeneity. Our analysis included six cohort studies comprising seven independent datasets and a total of 15,730,432 participants, among whom 83,351 incident TC cases were identified during follow-up periods ranging from 2.7 to 12.0 years. The results indicated that MetS was associated with a significantly increased risk of TC (RR = 1.26, 95% CI 1.10-1.46; p < 0.001), exhibiting substantial heterogeneity (I² = 91%). This association was consistent across prospective and retrospective cohorts, varying sample sizes, follow-up durations, and different strata of TC incidence (all p for subgroup differences > 0.05).  Moreover, sex-specific analyses revealed comparable associations in both men and women. Studies with higher methodological quality (Newcastle-Ottawa Scale score = 9) demonstrated a diminished yet still significant association compared to those with scores of 7-8 (RR = 1.15 vs. 1.80; p for subgroup difference < 0.001). In conclusion, MetS is associated with a moderately increased risk of TC in adults. However, due to the observational nature of the included studies and the potential for residual confounding, these findings should be interpreted as an association rather than definitive evidence of a causal relationship.

Indexed as

Metabolic SyndromeThyroid NeoplasmsAdultFemaleHumansIncidenceMaleRisk Factors

Identifiers

PMID42047117
PMCPMC13667998

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.