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rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis.
Teo, Kevin; Abeysekera, Kushala W M; Adams, Leon; Aigner, Elmar; Anstee, Quentin M; Banales, Jesus M; Banerjee, Rajarshi; Basu, Priyadarshi; Berg, Thomas; Bhatnagar, Pallav; Buch, Stephan; Canbay, Ali; Caprio, Sonia; Chatterjee, Ankita; Ida Chen, Yii-Der; Chowdhury, Abhijit; Daly, Ann K; Datz, Christian; de Gracia Hahn, Dana; DiStefano, Johanna K; Dong, Jiawen; Duret, Amedine; Emdin, Connor; Fairey, Madison; Gerhard, Glenn S; Guo, Xiuqing; Hampe, Jochen; Hickman, Matthew; Heintz, Lena; Hudert, Christian; Hunter, Harriet; Kelly, Matt; Kozlitina, Julia; Krawczyk, Marcin; Lammert, Frank; Langenberg, Claudia; Lavine, Joel; Li, Lin; Lim, Hong Kai; Loomba, Rohit; Luukkonen, Panu K; Melton, Phillip E; Mori, Trevor A; Palmer, Nicholette D; Parisinos, Constantinos A; Pillai, Sreekumar G; Qayyum, Faiza; Reichert, Matthias C; Romeo, Stefano; Rotter, Jerome I.
Afiliação
  • Teo K; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Abeysekera KWM; MRC Integrative Epidemiology Unit (IEU), University of Bristol, Bristol, UK.
  • Adams L; Medical School, Faculty of Health and Medical Sciences, University of Western Australia, Perth, WA, Australia; Department of Hepatology, Sir Charles Gairdner Hospital, Perth, WA, Australia.
  • Aigner E; First Department of Medicine, Paracelsus Medical University Salzburg, Austria.
  • Anstee QM; Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK; Newcastle NIHR Biomedical Research Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Banales JM; Department on Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, University of the Basque Country (UPV/EHU), CIBERehd, Ikerbasque, San Sebastian, Spain.
  • Banerjee R; Perspectum Ltd, Oxford, UK.
  • Basu P; National Institute of Biomedical Genomics, Kalyani, India.
  • Berg T; Division of Hepatology, Department of Medicine II, Leipzig University Medical Center, Leipzig, Germany.
  • Bhatnagar P; Eli Lilly and Company, Indianapolis, IN, USA.
  • Buch S; Medical Department 1, University Hospital Dresden, Technische Universität Dresden (TU Dresden), Dresden, Germany.
  • Canbay A; Gastroenterology, Hepatology and Infectiology, Otto-von-Guericke University Magdeburg, Magdeburg, Germany.
  • Caprio S; Yale University, Department of Pediatrics, New Haven, CT, USA.
  • Chatterjee A; National Institute of Biomedical Genomics, Kalyani, India.
  • Ida Chen YD; The Institute for Translational Genomics and Population Sciences, Department of Pediatrics, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
  • Chowdhury A; Institute of Post Graduate Medical Education and Research, Kolkata, India.
  • Daly AK; Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
  • Datz C; Department of Internal Medicine, General Hospital Oberndorf, Teaching Hospital of the Paracelsus Medical University Salzburg, Oberndorf, Austria.
  • de Gracia Hahn D; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • DiStefano JK; Diabetes and Fibrotic Disease Unit Translational Genomics Research Institute (TGen), Phoenix, AZ, USA.
  • Dong J; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Duret A; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Emdin C; Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Boston, MA, USA.
  • Fairey M; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Gerhard GS; Department of Medical Genetics and Molecular Biochemistry, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.
  • Guo X; The Institute for Translational Genomics and Population Sciences, Department of Pediatrics, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
  • Hampe J; Medical Department 1, University Hospital Dresden, Technische Universität Dresden (TU Dresden), Dresden, Germany.
  • Hickman M; MRC Integrative Epidemiology Unit (IEU), University of Bristol, Bristol, UK.
  • Heintz L; Department of Medicine II, Saarland University Medical Center, Saarland University, Homburg, Germany.
  • Hudert C; Department of Pediatric Gastroenterology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Hunter H; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Kelly M; Perspectum Ltd, Oxford, UK.
  • Kozlitina J; Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Krawczyk M; Department of Medicine II, Saarland University Medical Center, Saarland University, Homburg, Germany; Laboratory of Metabolic Liver Diseases, Department of General, Transplant and Liver Surgery, Centre for Preclinical Research, Medical University of Warsaw, Warsaw, Poland.
  • Lammert F; Department of Medicine II, Saarland University Medical Center, Saarland University, Homburg, Germany.
  • Langenberg C; MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge, UK.
  • Lavine J; Department of Pediatrics, Columbia University, New York, NY, USA.
  • Li L; BioStat Solutions LLC, Frederick, MD, USA.
  • Lim HK; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Loomba R; NAFLD Research Center, Division of Gastroenterology and Epidemiology, University of California at San Diego, La Jolla, CA, USA.
  • Luukkonen PK; Minerva Foundation Institute for Medical Research, Helsinki, Finland; Department of Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland; Yale University School of Medicine, New Haven, CT, USA.
  • Melton PE; School of Global Population Health, Faculty of Health and Medical Sciences, The University of Western Australia, Perth, WA, Australia; School of Pharmacy and Biomedical Sciences, Faculty of Health Sciences, Curtin University, Perth, WA, Australia; Menzies Institute for Medical Research, College of H
  • Mori TA; Medical School, Faculty of Health and Medical Sciences, University of Western Australia, Perth, WA, Australia.
  • Palmer ND; Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC, USA.
  • Parisinos CA; Institute of Health Informatics, Faculty of Population Health Sciences, University College London, London, UK.
  • Pillai SG; Eli Lilly and Company, Indianapolis, IN, USA.
  • Qayyum F; Department of Clinical Biochemistry, Rigshospitalet Copenhagen University Hospital, Copenhagen, Denmark.
  • Reichert MC; Department of Medicine II, Saarland University Medical Center, Saarland University, Homburg, Germany.
  • Romeo S; Department of Molecular and Clinical Medicine, University of Gothenburg, Gothenburg, Sweden; Cardiology Department, Sahlgrenska University Hospital, Gothenburg, Sweden; Clinical Nutrition Unit, Department of Medical and Surgical Sciences, University Magna Graecia, Catanzaro, Italy.
  • Rotter JI; The Institute for Translational Genomics and Population Sciences, Department of Pediatrics, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
J Hepatol ; 74(1): 20-30, 2021 01.
Article em En | MEDLINE | ID: mdl-32882372
ABSTRACT
BACKGROUND &

AIMS:

A common genetic variant near MBOAT7 (rs641738C>T) has been previously associated with hepatic fat and advanced histology in NAFLD; however, these findings have not been consistently replicated in the literature. We aimed to establish whether rs641738C>T is a risk factor across the spectrum of NAFLD and to characterise its role in the regulation of related metabolic phenotypes through a meta-analysis.

METHODS:

We performed a meta-analysis of studies with data on the association between rs641738C>T genotype and liver fat, NAFLD histology, and serum alanine aminotransferase (ALT), lipids or insulin. These included directly genotyped studies and population-level data from genome-wide association studies (GWAS). We performed a random effects meta-analysis using recessive, additive and dominant genetic models.

RESULTS:

Data from 1,066,175 participants (9,688 with liver biopsies) across 42 studies were included in the meta-analysis. rs641738C>T was associated with higher liver fat on CT/MRI (+0.03 standard deviations [95% CI 0.02-0.05], pz = 4.8×10-5) and diagnosis of NAFLD (odds ratio [OR] 1.17 [95% CI 1.05-1.3], pz = 0.003) in Caucasian adults. The variant was also positively associated with presence of advanced fibrosis (OR 1.22 [95% CI 1.03-1.45], pz = 0.021) in Caucasian adults using a recessive model of inheritance (CC + CT vs. TT). Meta-analysis of data from previous GWAS found the variant to be associated with higher ALT (pz = 0.002) and lower serum triglycerides (pz = 1.5×10-4). rs641738C>T was not associated with fasting insulin and no effect was observed in children with NAFLD.

CONCLUSIONS:

Our study validates rs641738C>T near MBOAT7 as a risk factor for the presence and severity of NAFLD in individuals of European descent. LAY

SUMMARY:

Fatty liver disease is a common condition where fat builds up in the liver, which can cause liver inflammation and scarring (including 'cirrhosis'). It is closely linked to obesity and diabetes, but some genes are also thought to be important. We did this study to see whether one specific change ('variant') in one gene ('MBOAT7') was linked to fatty liver disease. We took data from over 40 published studies and found that this variant near MBOAT7 is linked to more severe fatty liver disease. This means that drugs designed to work on MBOAT7 could be useful for treating fatty liver disease.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aciltransferases / Hepatopatia Gordurosa não Alcoólica / Fígado / Cirrose Hepática / Proteínas de Membrana Tipo de estudo: Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aciltransferases / Hepatopatia Gordurosa não Alcoólica / Fígado / Cirrose Hepática / Proteínas de Membrana Tipo de estudo: Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article