# Association between hypothyroidism and risk of chronic kidney disease: evidence from a systematic review and meta-analysis

**Authors:** Wei-Kun Zhuang, Xin-Yu Hu, Yun-Jia An, De-Liang Liu, Hui-Lin Li

PMC · DOI: 10.3389/fendo.2026.1704228 · Frontiers in Endocrinology · 2026-02-11

## TL;DR

This study finds a link between hypothyroidism and increased risk of chronic kidney disease, based on a review and analysis of multiple studies.

## Contribution

The study provides a systematic review and meta-analysis confirming hypothyroidism as a risk factor for CKD.

## Key findings

- Hypothyroidism is significantly associated with CKD in cross-sectional studies (OR = 1.66).
- Cohort studies also show hypothyroidism increases CKD risk (HR = 1.21).
- The association remains significant after adjusting for publication bias.

## Abstract

Chronic kidney disease (CKD) has become a significant issue in global public health, with its prevalence showing a persistent upward trend. Traditional risk factors cannot fully explain the persistent increase in incidence rates. Hypothyroidism, a common endocrine disorder, is considered a potential non-traditional risk factor for CKD, but the evidence remains inconsistent. This study aims to systematically evaluate the association between hypothyroidism and CKD risk.

Search PubMed, Embase, Web of Science, and Cochrane Library databases for relevant literature up to September 1, 2025. Included observational studies reporting the association between overt or subclinical hypothyroidism and CKD risk, providing odds ratios (OR) or hazard ratios (HR) with 95% confidence intervals (CIs). Quality assessment was conducted using the Newcastle–Ottawa Scale (NOS) and the Agency for Healthcare Research and Quality (AHRQ) quality assessment tool. Calculate pooled risk estimates using random-effects models, and conduct subgroup analyses, sensitivity analyses, and publication bias analyses.

A total of 13 publications reporting 15 studies (11 cross-sectional and 4 cohort studies) involving approximately 5,101,102 participants were included. The pooled analysis of cross-sectional studies demonstrated that hypothyroidism was significantly associated with CKD (OR = 1.66, 95% CI: 1.43–1.94; I² = 78.6%). Subgroup analyses revealed consistent associations across different thyroid disease types, regions, diagnostic methods, and study quality group. Pooled results from cohort studies also demonstrated that hypothyroidism significantly increased CKD risk (HR = 1.21, 95% CI 1.08-1.36; I² = 50.08%). Sensitivity analysis results remained stable. Publication bias was present in cross-sectional studies, but the association remained significant after using the trim-and-fill method (adjusted OR = 1.29, 95% CI: 1.06–1.57).

This systematic review and meta-analysis suggests that hypothyroidism is associated with an increased risk of CKD. Future well-designed prospective and interventional studies are needed to clarify temporal and causal relationships and to elucidate the underlying mechanisms between hypothyroidism and renal dysfunction.

https://www.crd.york.ac.uk/prospero/, identifier CRD420251143834.

## Linked entities

- **Diseases:** chronic kidney disease (MONDO:0005300), hypothyroidism (MONDO:0005420)

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** D-LL (MESH:D014808), renal function (MESH:D058186), thyroid disease (MESH:D013959), tubulointerstitial (MESH:D009395), kidney abnormalities (MESH:D007674), obesity (MESH:D009765), metabolic dysregulation (MESH:D021081), proteinuria (MESH:D011507), Hypothyroidism (MESH:D007037), dyslipidemia (MESH:D050171), hypertension (MESH:D006973), inflammation (MESH:D007249), glomerulosclerosis (MESH:D005921), albuminuria (MESH:D000419), hyponatremia (MESH:D007010), CKD (MESH:D051436), cardiovascular disease (MESH:D002318), kidney insufficiency (MESH:D051437), endocrine disorder (MESH:D004700), thyroid insufficiency (MESH:D000309), chronic renal failure (MESH:D007676), diabetes (MESH:D003920)
- **Chemicals:** water (MESH:D014867), creatinine (MESH:D003404), alcohol (MESH:D000438), salt (MESH:D012492), sodium (MESH:D012964), levothyroxine (MESH:D013974), FT4 (-), aldosterone (MESH:D000450)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

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## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932160/full.md

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Source: https://tomesphere.com/paper/PMC12932160