Relationship between genetic variation at PPP1R3B and levels of liver glycogen and triglyceride

• DOI: 10.1002/hep.29751
• Publication Date: 2017-12-23T13:53:34Z
• Authors: Stefan Stender; Eriks Smagris; Bo K. Lauridsen; Klaus F. Kofoed; Børge G. Nordestg...; Anne Tybjærg‐Hansen; Len A. Pennacchio; Diane E. Dickel; Jonathan C. Cohen; Helen H. Hobbs
• Keywords: Adult; Male; 0301 basic medicine; Clinical Sciences; Immunology; Chronic Liver Disease and Cirrhosis; 610; Clinical sciences; Medical Biochemistry and Metabolomics; Mice; 03 medical and health sciences; Protein Phosphatase 1; 616; Genetics; 2.1 Biological and endogenous factors; Animals; Humans; Triglycerides; Aged; Biomedical and Clinical Sciences; Gastroenterology & Hepatology; Liver Disease; Genetic Variation; Middle Aged; Liver Glycogen; Liver; Female; Digestive Diseases

Genetic variation at rs4240624 on chromosome 8 is associated with an attenuated signal on hepatic computerized tomography, which has been attributed to changes in hepatic fat. The closest coding gene to rs4240624, PPP1R3B, encodes a protein that promotes hepatic glycogen synthesis. Here, we performed studies to determine whether the x‐ray attenuation associated with rs4240624 is due to differences in hepatic glycogen or hepatic triglyceride content (HTGC). A sequence variant in complete linkage disequilibrium with rs4240624, rs4841132, was genotyped in the Dallas Heart Study (DHS), the Dallas Liver Study, and the Copenhagen Cohort (n = 112,428) of whom 1,539 had nonviral liver disease. The minor A‐allele of rs4841132 was associated with increased hepatic x‐ray attenuation (n = 1,572; P = 4 × 10–5), but not with HTGC (n = 2,674; P = 0.58). Rs4841132‐A was associated with modest, but significant, elevations in serum alanine aminotransferase (ALT) in the Copenhagen Cohort (P = 3 × 10–4) and the DHS (P = 0.004), and with odds ratios for liver disease of 1.13 (95% CI, 0.97‐1.31) and 1.23 (1.01‐1.51), respectively. Mice lacking protein phosphatase 1 regulatory subunit 3B (PPP1R3B) were deficient in hepatic glycogen, whereas HTGC was unchanged. Hepatic overexpression of PPP1R3B caused accumulation of hepatic glycogen and elevated plasma levels of ALT, but did not change HTGC. Conclusion: These observations are consistent with the notion that the minor allele of rs4841132 promotes a mild form of hepatic glycogenosis that is associated with hepatic injury. (Hepatology 2018;67:2182‐2195).