Upper limit of normal ALT levels in health and metabolic diseases: Pooled analysis of 423,355 individuals with bootstrap modelling

Author:

Tan Eunice X.12,Huang Daniel Q.12ORCID,Yee Natasha Tang Sook2,Wan Zi Hui2,Nerurkar Sanjna N.2,Kai Justin Chua Ying2,Goh Kang Shiong1,Ng Cheng Han12ORCID,Muthiah Mark12ORCID,Zhou Yu3,Woodward Amanda4,Le Michael H.56,Yeo Yee Hui7ORCID,Barnett Scott5,Cheung Ramsey58,Nguyen Mindie H.59ORCID

Affiliation:

1. Division of Gastroenterology and Hepatology, Department of Medicine National University Hospital Singapore Singapore

2. Department of Medicine, Yong Loo Lin School of Medicine National University of Singapore Singapore Singapore

3. Adelaide Medical School The University of Adelaide Adelaide South Australia Australia

4. Lane Medical Library Stanford University Stanford California USA

5. Division of Gastroenterology and Hepatology, Department of Medicine Stanford University Medical Center Palo Alto California USA

6. Larner College of Medicine at the University of Vermont Burlington Vermont USA

7. Division of General Internal Medicine Cedars‐Sinai Medical Center Los Angeles California USA

8. Division of Gastroenterology and Hepatology Veterans Affairs Palo Alto Health Care System Palo Alto California USA

9. Department of Epidemiology and Population Health Stanford University School of Medicine Stanford California USA

Abstract

SummaryIntroductionGiven the global rise in obesity‐related metabolic diseases, the upper limit of normal (ULN) alanine aminotransferase (ALT) in individuals with and without metabolic diseases may have changed. We performed a meta‐analysis combined with bootstrap modelling to estimate the ALT ULN levels for individuals with and without metabolic diseases.Methods and ResultsTwo separate searches of the PubMed, Embase and Cochrane databases were performed, one to identify healthy individuals which yielded 12 articles (349,367 individuals); another to include those with potential metabolic diseases but without known liver disease which yielded 35 articles (232,388 individuals). We estimated the mean ALT using a random‐effects mixed model and the ULN level (95th‐percentile value) via a bootstrap model with 10,000 resamples. In individuals without metabolic diseases and known liver disease, the ALT ULN levels were 32 U/L overall; 36 U/L in males and 28 U/L in females. In analyses that included individuals with metabolic diseases, the ALT ULN levels were 40 U/L among the overweight/obese (29 U/L if normal weight) and 36 U/L among those with type 2 diabetes mellitus (T2DM) (33 U/L if no T2DM). On meta‐regression of study‐level factors, body mass index (coefficient 1.49, 95% CI 0.11–2.86, p = 0.03), high‐density lipoprotein (coefficient −0.47, 95% CI −0.85‐(−0.08), p = 0.02) and triglycerides (coefficient 0.19, 95% CI 0.12–0.25, p < 0.0001) correlated with ALT.ConclusionWe provide expected ranges of ALT ULN levels for individuals without known liver disease without metabolic diseases and those with or without T2DM and/or are normal weight or overweight/obese. These data may have implications for clinical care and screening.

Publisher

Wiley

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