» Articles » PMID: 22105854

Variant in the Glucokinase Regulatory Protein (GCKR) Gene is Associated with Fatty Liver in Obese Children and Adolescents

Overview
Journal Hepatology
Specialty Gastroenterology
Date 2011 Nov 23
PMID 22105854
Citations 110
Authors
Affiliations
Soon will be listed here.
Abstract

Unlabelled: Recently, the single nucleotide polymorphism (SNP) identified as rs1260326, in the glucokinase regulatory protein (GCKR), was associated with hypertriglyceridemia in adults. Because accumulation of triglycerides in hepatocytes represents the hallmark of steatosis, we aimed to investigate whether this variant might be associated with fatty liver (hepatic fat content, HFF%). Moreover, because recently rs738409 in the PNPLA3 and rs2854116 in the APOC3 were associated with fatty liver, we explored how the GCKR SNP and these two variants jointly influence hepatosteatosis. We studied 455 obese children and adolescents (181 Caucasians, 139 African Americans, and 135 Hispanics). All underwent an oral glucose tolerance test and fasting lipoprotein subclasses measurement by proton nuclear magnetic resonance. A subset of 142 children underwent a fast gradient magnetic resonance imaging to measure the HFF%. The rs1260326 was associated with elevated triglycerides (Caucasians P = 0.00014; African Americans P = 0.00417), large very low-density lipoprotein (VLDL) (Caucasians P = 0.001; African Americans, P = 0.03), and with fatty liver (Caucasians P = 0.034; African Americans P = 0.00002; and Hispanics P = 0.016). The PNPLA3, but not the APOC3 rs2854116 SNP, was associated with fatty liver but not with triglyceride levels. There was a joint effect between the PNPLA3 and GCKR SNPs, explaining 32% of HFF% variance in Caucasians (P = 0.00161), 39.0% in African Americans (P = 0.00000496), and 15% in Hispanics (P = 0.00342).

Conclusion: The rs1260326 in GCKR is associated with hepatic fat accumulation along with large VLDL and triglyceride levels. GCKR and PNPLA3 act together to convey susceptibility to fatty liver in obese youths.

Citing Articles

Glucokinase activator improves glucose tolerance and induces hepatic lipid accumulation in mice with diet-induced obesity.

Cai N, Chen X, Liu J, Wen Z, Wen S, Zeng W Liver Res. 2025; 7(2):124-135.

PMID: 39958949 PMC: 11791924. DOI: 10.1016/j.livres.2023.05.003.


Genetic Risk Factors for Metabolic Dysfunction-Associated Steatotic Liver Disease.

Pei Y, Goh G Gut Liver. 2025; 19(1):8-18.

PMID: 39774124 PMC: 11736312. DOI: 10.5009/gnl240407.


Dysfunctional VLDL metabolism in MASLD.

Marigorta U, Millet O, Lu S, Mato J NPJ Metab Health Dis. 2024; 2(1):16.

PMID: 39049993 PMC: 11263124. DOI: 10.1038/s44324-024-00018-1.


Interplay between gut microbiome, host genetic and epigenetic modifications in MASLD and MASLD-related hepatocellular carcinoma.

Ha S, Wong V, Zhang X, Yu J Gut. 2024; 74(1):141-152.

PMID: 38950910 PMC: 11671994. DOI: 10.1136/gutjnl-2024-332398.


Association of GCKR and MBOAT7 genetic polymorphisms with non-alcoholic fatty liver disease.

Chavan S, Rathi P, Mandot A Clin Exp Hepatol. 2024; 10(1):39-46.

PMID: 38765903 PMC: 11100339. DOI: 10.5114/ceh.2024.136326.


References
1.
Kozlitina J, Boerwinkle E, Cohen J, Hobbs H . Dissociation between APOC3 variants, hepatic triglyceride content and insulin resistance. Hepatology. 2011; 53(2):467-74. PMC: 3057507. DOI: 10.1002/hep.24072. View

2.
Valenti L, Alisi A, Galmozzi E, Bartuli A, del Menico B, Alterio A . I148M patatin-like phospholipase domain-containing 3 gene variant and severity of pediatric nonalcoholic fatty liver disease. Hepatology. 2010; 52(4):1274-80. DOI: 10.1002/hep.23823. View

3.
Browning J, Cohen J, Hobbs H . Patatin-like phospholipase domain-containing 3 and the pathogenesis and progression of pediatric nonalcoholic fatty liver disease. Hepatology. 2010; 52(4):1189-92. PMC: 3135009. DOI: 10.1002/hep.23946. View

4.
Dongiovanni P, Valenti L, Rametta R, Daly A, Nobili V, Mozzi E . Genetic variants regulating insulin receptor signalling are associated with the severity of liver damage in patients with non-alcoholic fatty liver disease. Gut. 2010; 59(2):267-73. DOI: 10.1136/gut.2009.190801. View

5.
Rasmussen-Torvik L, Li M, Kao W, Couper D, Boerwinkle E, Bielinski S . Association of a fasting glucose genetic risk score with subclinical atherosclerosis: The Atherosclerosis Risk in Communities (ARIC) study. Diabetes. 2010; 60(1):331-5. PMC: 3012190. DOI: 10.2337/db10-0839. View