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Peer-reviewedCC BY 4.0Frontiers in Endocrinology

Association of remnant cholesterol with kidney outcomes in adults with type 2 diabetes: a systematic review and meta-analysis

4 affiliations
  1. 1The First Clinical Medical College, Yan'an Medical College, Yan'an University
  2. 2Yan'an Medical College, Yan'an University
  3. 3Department of Endocrinology, Affiliated Hospital of Yan'an University
  4. 4Department of Nephrology, The Second Affiliated Hospital of Xi’an Jiaotong University

Abstract

Introduction: Remnant cholesterol (RC) reflects the cholesterol carried by triglyceride-rich lipoprotein remnants and may capture lipid-related kidney risk not fully represented by conventional lipid measures. We evaluated the associations between RC and kidney outcomes in adults with type 2 diabetes mellitus (T2DM).

Methods: Following PRISMA 2020, PubMed/MEDLINE, Scopus, the Cochrane Library, Google Scholar, Wiley Online Library, and ScienceDirect were searched for longitudinal and cross-sectional observational studies evaluating circulating RC and kidney outcomes in adults with T2DM. Studies of mixed populations were eligible only when T2DM-specific data could be extracted. Adjusted effect estimates were pooled separately by study design and kidney outcome using restricted maximum likelihood random-effects models with Hartung–Knapp adjustment.

Results: Seventeen articles contributed 18 independent estimates from 2,817,820 participants with T2DM. The exploratory all-study model showed an association between higher RC and adverse kidney outcomes (association ratio 1.50, 95% CI 1.32–1.72, P < 0.001; I ² = 87.6%). The longitudinal model, comprising 12 independent estimates from 11 articles, showed a similar association (HR 1.27, 95% CI 1.17–1.37, P < 0.001; I ² = 42.9%). Outcome-specific analyses showed an association with incident diabetic kidney disease (DKD; HR 1.27, 95% CI 1.15–1.41, P = 0.0029). The estimate for kidney failure/end-stage kidney disease was positive but not statistically significant (HR 1.56, 95% CI 0.82–2.97, P = 0.115). The association with DKD progression also did not reach statistical significance (HR 1.17, 95% CI 1.00–1.37, P = 0.052), while one study reported an association with incident albuminuria (HR 1.23, 95% CI 1.06–1.43, P = 0.007). Six cross-sectional studies showed an association between higher RC and prevalent or early DKD in adults with T2DM (OR 2.03, 95% CI 1.71–2.42, P < 0.001; I ² = 2.5%). The longitudinal association remained after restricting the analysis to estimates adjusted for blood pressure, glycemia, and adiposity (HR 1.28, 95% CI 1.21–1.37, P < 0.001). A smaller subset that included continuous estimates showed that a 0.1 mmol/L increase in RC was not associated with incident DKD (HR 1.02, 95% CI 0.98–1.07, P = 0.197).

Conclusions: Higher RC was associated with incident and prevalent DKD and with adverse longitudinal kidney outcomes overall in adults with T2DM. RC may serve as a complementary kidney-risk marker, but the observational evidence does not establish causality or a clinical threshold.

Systematic review registration : https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD420261475085 , identifier CRD420261475085.

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BibTeX
@article{gao2026association,
  title = {{Association of remnant cholesterol with kidney outcomes in adults with type 2 diabetes: a systematic review and meta-analysis}},
  author = {Jie Gao and Jiaqi Wang and Zhangli Wang},
  journal = {Frontiers in Endocrinology},
  year = {2026},
  month = oct,
  doi = {10.3389/fendo.2026.1969361},
  url = {https://www.frontiersin.org/articles/10.3389/fendo.2026.1969361/full},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Association of remnant cholesterol with kidney outcomes in adults with type 2 diabetes: a systematic review and meta-analysis
AU  - Jie Gao
AU  - Jiaqi Wang
AU  - Zhangli Wang
PY  - 2026
DA  - 2026/10/16
JO  - Frontiers in Endocrinology
DO  - 10.3389/fendo.2026.1969361
UR  - https://www.frontiersin.org/articles/10.3389/fendo.2026.1969361/full
AB  - Introduction: Remnant cholesterol (RC) reflects the cholesterol carried by triglyceride-rich lipoprotein remnants and may capture lipid-related kidney risk not fully represented by conventional lipid measures. We evaluated the associations between RC and kidney outcomes in adults with type 2 diabetes mellitus (T2DM).  Methods: Following PRISMA 2020, PubMed/MEDLINE, Scopus, the Cochrane Library, Google Scholar, Wiley Online Library, and ScienceDirect were searched for longitudinal and cross-sectional observational studies evaluating circulating RC and kidney outcomes in adults with T2DM. Studies of mixed populations were eligible only when T2DM-specific data could be extracted. Adjusted effect estimates were pooled separately by study design and kidney outcome using restricted maximum likelihood random-effects models with Hartung–Knapp adjustment.  Results: Seventeen articles contributed 18 independent estimates from 2,817,820 participants with T2DM. The exploratory all-study model showed an association between higher RC and adverse kidney outcomes (association ratio 1.50, 95% CI 1.32–1.72, P < 0.001; I ² = 87.6%). The longitudinal model, comprising 12 independent estimates from 11 articles, showed a similar association (HR 1.27, 95% CI 1.17–1.37, P < 0.001; I ² = 42.9%). Outcome-specific analyses showed an association with incident diabetic kidney disease (DKD; HR 1.27, 95% CI 1.15–1.41, P = 0.0029). The estimate for kidney failure/end-stage kidney disease was positive but not statistically significant (HR 1.56, 95% CI 0.82–2.97, P = 0.115). The association with DKD progression also did not reach statistical significance (HR 1.17, 95% CI 1.00–1.37, P = 0.052), while one study reported an association with incident albuminuria (HR 1.23, 95% CI 1.06–1.43, P = 0.007). Six cross-sectional studies showed an association between higher RC and prevalent or early DKD in adults with T2DM (OR 2.03, 95% CI 1.71–2.42, P < 0.001; I ² = 2.5%). The longitudinal association remained after restricting the analysis to estimates adjusted for blood pressure, glycemia, and adiposity (HR 1.28, 95% CI 1.21–1.37, P < 0.001). A smaller subset that included continuous estimates showed that a 0.1 mmol/L increase in RC was not associated with incident DKD (HR 1.02, 95% CI 0.98–1.07, P = 0.197).  Conclusions: Higher RC was associated with incident and prevalent DKD and with adverse longitudinal kidney outcomes overall in adults with T2DM. RC may serve as a complementary kidney-risk marker, but the observational evidence does not establish causality or a clinical threshold.  Systematic review registration : https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD420261475085 , identifier CRD420261475085.
SN  - 1664-2392
ER  -