Variations in Estimated Glomerular Filtration Rate Across Countries in Patients With Metabolic Dysfunction-Associated Steatotic Liver Disease and Their Association With Liver Fibrosis: A Multicenter Study

Jing Zhao , Ferenc E. Mózes , Xin-Yu Xu , Dong Ji , Huiqing Liang , Xiaoling Chi , Jinjun Chen , Takeshi Okanoue , Toshihide Shima , Yongfen Zhu , Christian Labenz , Bihui Zhong , Masato Yoneda , Atsushi Nakajima , Junping Shi , Jing Zhang , Sanjiv Mahadeva , Wah-Kheong Chan , Fangping He , Chun-Yan Ye , Su Lin , Adèle Delamarre , Victor de Lédinghen , Monica Lupsor-Platon , Zhonghua Lu , Hong Tang , Jidong Jia , Peter J. Eddowes , Liang Xu , Yiling Li , Yuemin Nan , Hong Deng , Junqi Niu , Xuebing Yan , Qing Ye , Qinglei Zeng , Yongjian Zhou , Jeremy F. L. Cobbold , Chenghai Liu , Jie Li , Lei Li , Jing Wang , Fanpu Ji , Jin Chai , Yongning Xin , Giovanni Targher , Christopher D. Byrne , Yuchen Fan , Jia-Hui Zhang , Geraldine Ooi , Jacob George , Michael Pavlides , Dan-Qin Sun , Ming-Hua Zheng

MedComm ›› 2025, Vol. 6 ›› Issue (12) : e70503

PDF
MedComm ›› 2025, Vol. 6 ›› Issue (12) :e70503 DOI: 10.1002/mco2.70503
ORIGINAL ARTICLE
Variations in Estimated Glomerular Filtration Rate Across Countries in Patients With Metabolic Dysfunction-Associated Steatotic Liver Disease and Their Association With Liver Fibrosis: A Multicenter Study
Author information +
History +
PDF

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) has become the most prevalent chronic liver disease globally. Previous studies have shown that MASLD is an independent risk factor for chronic kidney disease (CKD), but the variations in estimated glomerular filtration rate (eGFR) levels across countries with different ethnic backgrounds have not been extensively reported. We enrolled 3308 participants with biopsy-proven MASLD from 34 centers in this multinational study and analyzed the associations between eGFR and histological severity of liver fibrosis in different countries. European participants had lower eGFR levels (92.2 ± 20.7 vs. 104.7 ± 17.3 mL/min/1.73 m2) and significant liver fibrosis (61.4 vs. 32.4%) than Asian individuals. In Asia, Chinese participants had the highest mean eGFR level at 105.8 mL/min/1.73 m2, while Malaysian participants had the lowest at 87.3 mL/min/1.73 m2 (p < 0.001). In Europe, French participants had the highest mean eGFR level at 95.3 mL/min/1.73 m2, while Romanian individuals had the lowest at 81.1 mL/min/1.73 m2 (p < 0.001). eGFR levels were inversely associated with liver fibrosis in Asian individuals (OR: 0.793, 95%CI: 0.685–0.917, p = 0.002), even after adjusting for traditional renal risk factors, but not in Europeans. Our findings provide the basis for further investigation of the burden of MASLD on CKD risk in different countries.

Keywords

epidemiology / estimated glomerular filtration rate / liver fibrosis / metabolic dysfunction-associated steatotic liver disease / metabolic dysfunction-associated fatty liver disease

Cite this article

Download citation ▾
Jing Zhao, Ferenc E. Mózes, Xin-Yu Xu, Dong Ji, Huiqing Liang, Xiaoling Chi, Jinjun Chen, Takeshi Okanoue, Toshihide Shima, Yongfen Zhu, Christian Labenz, Bihui Zhong, Masato Yoneda, Atsushi Nakajima, Junping Shi, Jing Zhang, Sanjiv Mahadeva, Wah-Kheong Chan, Fangping He, Chun-Yan Ye, Su Lin, Adèle Delamarre, Victor de Lédinghen, Monica Lupsor-Platon, Zhonghua Lu, Hong Tang, Jidong Jia, Peter J. Eddowes, Liang Xu, Yiling Li, Yuemin Nan, Hong Deng, Junqi Niu, Xuebing Yan, Qing Ye, Qinglei Zeng, Yongjian Zhou, Jeremy F. L. Cobbold, Chenghai Liu, Jie Li, Lei Li, Jing Wang, Fanpu Ji, Jin Chai, Yongning Xin, Giovanni Targher, Christopher D. Byrne, Yuchen Fan, Jia-Hui Zhang, Geraldine Ooi, Jacob George, Michael Pavlides, Dan-Qin Sun, Ming-Hua Zheng. Variations in Estimated Glomerular Filtration Rate Across Countries in Patients With Metabolic Dysfunction-Associated Steatotic Liver Disease and Their Association With Liver Fibrosis: A Multicenter Study. MedComm, 2025, 6(12): e70503 DOI:10.1002/mco2.70503

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

G. Feng, L. Valenti, V. W. Wong, et al., “Recompensation in Cirrhosis: Unravelling the Evolving Natural History of Nonalcoholic Fatty Liver Disease,” Nature Reviews Gastroenterology & Hepatology 21, no. 1 (2024): 46–56.

[2]

G. E. H. Lim, A. Tang, C. H. Ng, et al., “An Observational Data Meta-analysis on the Differences in Prevalence and Risk Factors between MAFLD vs NAFLD,” Clinical Gastroenterology and Hepatology: the Official Clinical Practice Journal of the American Gastroenterological Association 21, no. 3 (2023): 619–629. e617.

[3]

L. Miao, G. Targher, C. D. Byrne, Y. Y. Cao, and M. H. Zheng, “Current Status and Future Trends of the Global Burden of MASLD,” Trends in Endocrinology and Metabolism: TEM 35, no. 8 (2024): 697–707.

[4]

M. Eslam, A. J. Sanyal, and J. George, “MAFLD: A Consensus-Driven Proposed Nomenclature for Metabolic Associated Fatty Liver Disease,” Gastroenterology 158, no. 7 (2020): 1999–2014. e1991.

[5]

A. De, N. Bhagat, M. Mehta, S. Taneja, and A. Duseja, “Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD) Definition Is Better Than MAFLD Criteria for Lean Patients With NAFLD,” Journal of Hepatology 80, no. 2 (2024): e61–e62.

[6]

K. I. Zheng, D. Q. Sun, Y. Jin, P. W. Zhu, and M. H. Zheng, “Clinical Utility of the MAFLD Definition,” Journal of Hepatology 74, no. 4 (2021): 989–991.

[7]

J. Zhou, D.-Q. Sun, G. Targher, et al., “Metabolic Dysfunction-associated Fatty Liver Disease Increases Risk of Chronic Kidney Disease: A Systematic Review and Meta-analysis,” Egastroenterology 1, no. 1 (2023): e100005.

[8]

V. H. Nguyen, M. H. Le, R. C. Cheung, and M. H. Nguyen, “Differential Clinical Characteristics and Mortality Outcomes in Persons with NAFLD and/or MAFLD,” Clinical Gastroenterology and Hepatology: the Official Clinical Practice Journal of the American Gastroenterological Association 19, no. 10 (2021): 2172–2181. e2176.

[9]

T. Y. Wang, R. F. Wang, Z. Y. Bu, et al., “Association of Metabolic Dysfunction-associated Fatty Liver Disease With Kidney Disease,” Nature Reviews Nephrology 18, no. 4 (2022): 259–268.

[10]

J. Zhao, L. Liu, Y. Y. Cao, et al., “MAFLD as Part of Systemic Metabolic Dysregulation,” Hepatology International 18, Suppl no. 2 (2024): 834–847.

[11]

J. Bilson, T. J. Hydes, D. McDonnell, et al., “Impact of Metabolic Syndrome Traits on Kidney Disease Risk in Individuals With MASLD: A UK Biobank Study,” Liver International: Official Journal of the International Association for the Study of the Liver 45, no. 4 (2025): e16159.

[12]

D. J. Cuthbertson, O. J. Kennedy, J. Bilson, et al., “Impact of Metabolic Dysfunction Severity in Steatotic Liver Disease and Its Interaction With Liver Fibrosis on all-cause Mortality and Multiple Hepatic and Extra-hepatic Outcomes,” Metabolism: Clinical and Experimental 170 (2025): 156306.

[13]

G. Collaboration, “Global, Regional, and National Burden of Chronic Kidney Disease, 1990-2017: A Systematic Analysis for the Global Burden of Disease Study 2017,” Lancet (London, England) 395, no. 10225 (2020): 709–733.

[14]

J. Hu, R. Ke, W. Teixeira, et al., “Global, Regional, and National Burden of CKD due to Glomerulonephritis From 1990 to 2019: A Systematic Analysis From the Global Burden of Disease Study 2019,” Clinical Journal of the American Society of Nephrology: CJASN 18, no. 1 (2023): 60–71.

[15]

D. Q. Sun, Y. Jin, and T. Y. Wang, “MAFLD and Risk of CKD,” Metabolism: Clinical and Experimental 115 (2021): 154433.

[16]

Y. Liang, H. Chen, Y. Liu, et al., “Association of MAFLD with Diabetes, Chronic Kidney Disease, and Cardiovascular Disease: A 4.6-Year Cohort Study in China,” The Journal of Clinical Endocrinology and Metabolism 107, no. 1 (2022): 88–97.

[17]

S. Chen, J. Pang, R. Huang, H. Xue, and X. Chen, “Association of MAFLD With End-stage Kidney Disease: A Prospective Study of 337,783 UK Biobank Participants,” Hepatology International 17, no. 3 (2023): 595–605.

[18]

C. Sun, G. B. Goh, W. C. Chow, et al., “Prevalence and Risk Factors for Impaired Renal Function Among Asian Patients With Nonalcoholic Fatty Liver Disease,” Hepatobiliary & Pancreatic Diseases International: HBPD INT 23, no. 3 (2023): 241–248.

[19]

D. Q. Sun, G. Targher, C. D. Byrne, et al., “An International Delphi Consensus Statement on Metabolic Dysfunction-associated Fatty Liver Disease and Risk of Chronic Kidney Disease,” Hepatobiliary Surgery and Nutrition 12, no. 3 (2023): 386–403.

[20]

L. A. Inker and S. Titan, “Measurement and Estimation of GFR for Use in Clinical Practice: Core Curriculum 2021,” American Journal of Kidney Diseases: the Official Journal of the National Kidney Foundation 78, no. 5 (2021): 736–749.

[21]

J. Coresh, T. C. Turin, K. Matsushita, et al., “Decline in Estimated Glomerular Filtration Rate and Subsequent Risk of End-stage Renal Disease and Mortality,” Jama 311, no. 24 (2014): 2518–2531.

[22]

A. Ramezankhani, F. Azizi, and F. Hadaegh, “Association Between Estimated Glomerular Filtration Rate Slope and Cardiovascular Disease Among Individuals With and Without Diabetes: A Prospective Cohort Study,” Cardiovascular Diabetology 22, no. 1 (2023): 270.

[23]

L. Liu, M. Zhu, Q. Meng, et al., “Association Between Kidney Function and the Risk of Cancer: Results From the China Health and Retirement Longitudinal Study (CHARLS),” Journal of Cancer 11, no. 21 (2020): 6429–6436.

[24]

D. Q. Sun, J. Q. Shen, X. F. Tong, et al., “Liver Fibrosis Progression Analyzed With AI Predicts Renal Decline,” JHEP Reports: Innovation in Hepatology 7, no. 5 (2025): 101358.

[25]

K. E. Chan, T. J. L. Koh, A. S. P. Tang, et al., “Global Prevalence and Clinical Characteristics of Metabolic-associated Fatty Liver Disease: A Meta-Analysis and Systematic Review of 10 739 607 Individuals,” The Journal of Clinical Endocrinology and Metabolism 107, no. 9 (2022): 2691–2700.

[26]

J. Liu, I. Ayada, X. Zhang, et al., “Estimating Global Prevalence of Metabolic Dysfunction-Associated Fatty Liver Disease in Overweight or Obese Adults,” Clinical Gastroenterology and Hepatology: the Official Clinical Practice Journal of the American Gastroenterological Association 20, no. 3 (2022): e573–e582.

[27]

W. Zhang, W. J. Song, W. Chen, et al., “Metabolic Dysfunction-associated Steatotic Liver Disease-related Hepatic Fibrosis Increases Risk of Insulin Resistance, Type 2 Diabetes, and Chronic Kidney Disease,” European Journal of Gastroenterology & Hepatology 36, no. 6 (2024): 802–810.

[28]

K. Brück, V. S. Stel, G. Gambaro, et al., “CKD Prevalence Varies Across the European General Population,” Journal of the American Society of Nephrology: JASN 27, no. 7 (2016): 2135–2147.

[29]

P. A. Kavsak and K. Nouri, “Low-risk Cutoff of 90 Ml/Min/1.73 M(2) for the Estimated Glomerular Filtration Rate and the Importance of the Equation for Patients With Acute Coronary Syndrome,” Clinica Chimica Acta; International Journal of Clinical Chemistry 523 (2021): 532–533.

[30]

M. L. Caramori, P. Fioretto, and M. Mauer, “Low Glomerular Filtration Rate in Normoalbuminuric Type 1 Diabetic Patients: An Indicator of More Advanced Glomerular Lesions,” Diabetes 52, no. 4 (2003): 1036–1040.

[31]

Y. Hashimoto, M. Tanaka, H. Okada, et al., “Metabolically Healthy Obesity and Risk of Incident CKD,” Clinical Journal of the American Society of Nephrology: CJASN 10, no. 4 (2015): 578–583.

[32]

K. Chintam and A. R. Chang, “Strategies to Treat Obesity in Patients with CKD,” American Journal of Kidney Diseases: the Official Journal of the National Kidney Foundation 77, no. 3 (2021): 427–439.

[33]

I. Helal, G. M. Fick-Brosnahan, B. Reed-Gitomer, and R. W. Schrier, “Glomerular Hyperfiltration: Definitions, Mechanisms and Clinical Implications,” Nature Reviews Nephrology 8, no. 5 (2012): 293–300.

[34]

D. C. Rockey, S. H. Caldwell, Z. D. Goodman, R. C. Nelson, and A. D. Smith, “Liver Biopsy,” Hepatology (Baltimore, Md) 49, no. 3 (2009): 1017–1044.

[35]

D. Q. Sun, F. Z. Ye, H. T. Kani, et al., “Higher Liver Stiffness Scores Are Associated With Early Kidney Dysfunction in Patients With Histologically Proven Non-cirrhotic NAFLD,” Diabetes & Metabolism 46, no. 4 (2020): 288–295.

[36]

J. Bai, L. Zhang, M. Zhang, Y. Hao, Z. Yi, and Y. Zhou, “Regional Insights Into the Relationship Between Metabolic Associated Steatotic Liver Disease and Chronic Kidney Disease: A Socioeconomic Perspective on Disease Correlation,” BMC Public Health [Electronic Resource] 25, no. 1 (2025): 993.

[37]

S. Chen, X. Xu, H. Gong, et al., “Global Epidemiological Features and Impact of Osteosarcopenia: A Comprehensive Meta-analysis and Systematic Review,” Journal of Cachexia, Sarcopenia and Muscle 15, no. 1 (2024): 8–20.

[38]

T. Abe, M. G. Bemben, M. Kondo, Y. Kawakami, and T. Fukunaga, “Comparison of Skeletal Muscle Mass to Fat-free Mass Ratios Among Different Ethnic Groups,” The Journal of Nutrition, Health & Aging 16, no. 6 (2012): 534–538.

[39]

I. Janssen, S. B. Heymsfield, R. N. Baumgartner, and R. Ross, “Estimation of Skeletal Muscle Mass by Bioelectrical Impedance Analysis,” Journal of Applied Physiology (Bethesda, Md: 1985) 89, no. 2 (2000): 465–471.

[40]

Z. M. Younossi, S. Zelber-Sagi, J. V. Lazarus, et al., “Global Consensus Recommendations for Metabolic Dysfunction-Associated Steatotic Liver Disease and Steatohepatitis,” Gastroenterology 169, no. 5 (2025): 1017–1032. e1012.

[41]

A. S. Levey, L. A. Stevens, C. H. Schmid, et al., “A New Equation to Estimate Glomerular Filtration Rate,” Annals of Internal Medicine 150, no. 9 (2009): 604–612.

[42]

C. Delgado, M. Baweja, D. C. Crews, et al., “A Unifying Approach for GFR Estimation: Recommendations of the NKF-ASN Task Force on Reassessing the Inclusion of Race in Diagnosing Kidney Disease,” American Journal of Kidney Diseases: the Official Journal of the National Kidney Foundation 79, no. 2 (2022): 268–288. e261.

[43]

A. J. Sanyal, R. Loomba, Q. M. Anstee, et al., “Utility of Pathologist Panels for Achieving Consensus in NASH Histologic Scoring in Clinical Trials: Data From a Phase 3 Study,” Hepatology Communications 8, no. 1 (2024): e0325.

[44]

D. E. Kleiner, E. M. Brunt, M. Van Natta, et al., “Design and Validation of a Histological Scoring System for Nonalcoholic Fatty Liver Disease,” Hepatology (Baltimore, Md) 41, no. 6 (2005): 1313–1321.

RIGHTS & PERMISSIONS

2025 The Author(s). MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd.

PDF

3

Accesses

0

Citation

Detail

Sections
Recommended

/