The Role of Phosphatidylethanolamine N-Methyltransferase (PEMT) and Its Waist-Hip-Ratio-Associated Locus rs4646404 in Obesity-Related Metabolic Traits and Liver Disease

• Published in: International journal of molecular sciences Vol. 24; no. 23; p. 16850
• Main Authors: Sun, Chang, Holstein, David J. F., Garcia-Cubero, Natalia, Moulla, Yusef, Stroh, Christine, Dietrich, Arne, Schön, Michael R., Gärtner, Daniel, Lohmann, Tobias, Dressler, Miriam, Stumvoll, Michael, Blüher, Matthias, Kovacs, Peter, Guiu-Jurado, Esther
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.12.2023
• Subjects: Adipose tissues; Age; Analysis; Body fat; Body mass index; Development and progression; Diabetes; Genetic aspects; Genomes; Genomics; Glucose; Homeostasis; Insulin resistance; Lipids; Liver diseases; Messenger RNA; Metabolism; Obesity; Phospholipids; Regression analysis; Single nucleotide polymorphisms; Transferases; Type 2 diabetes; Germany; adipose tissue; fat distribution; PEMT; rs4646404; liver disease; obesity
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms242316850

In previous genome-wide association studies (GWAS), genetic loci associated with obesity and impaired fat distribution (FD) have been identified. In the present study, we elucidated the role of the PEMT gene, including the waist–hip-ratio-associated single nucleotide polymorphism rs4646404, and its influence on obesity-related metabolic traits. DNA from 2926 metabolically well-characterized subjects was used for genotyping. PEMT expression was analyzed in paired visceral (vis) and subcutaneous (sc) adipose tissue (AT) from a subset of 574 individuals. Additionally, PEMT expression was examined in vis, sc AT and liver tissue in a separate cohort of 64 patients with morbid obesity and liver disease. An in vitro Pemt knockdown was conducted in murine epididymal and inguinal adipocytes. Our findings highlight tissue-specific variations in PEMT mRNA expression across the three studied tissues. Specifically, vis PEMT mRNA levels correlated significantly with T2D and were implicated in the progression of non-alcoholic steatohepatitis (NASH), in contrast to liver tissue, where no significant associations were found. Moreover, sc PEMT expression showed significant correlations with several anthropometric- and metabolic-related parameters. The rs4646404 was associated with vis AT PEMT expression and also with diabetes-related traits. Our in vitro experiments supported the influence of PEMT on adipogenesis, emphasizing its role in AT biology. In summary, our data suggest that PEMT plays a role in regulating FD and has implications in metabolic diseases.