PNPLA3 and SAMM50 variants are associated with lean nonalcoholic fatty liver disease in Asian population

被引:0
|
作者
Lu, Chia-Wen [1 ,2 ,3 ]
Chou, Tzu-Jung [1 ,2 ,4 ]
Wu, Tsan-Yu [2 ]
Lee, Yi-Hsuan [1 ,3 ]
Yang, Hung-Jen [5 ,6 ]
Huang, Kuo-Chin [2 ,3 ,4 ]
机构
[1] Natl Taiwan Univ, Grad Inst Clin Med, Coll Med, Taipei, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Family Med, Taipei, Taiwan
[3] Natl Taiwan Univ, Coll Med, Dept Family Med, Taipei, Taiwan
[4] Natl Taiwan Univ Hosp, Hsin Chu Branch, Dept Family Med, Taipei, Hsin Chu, Taiwan
[5] Min Sheng Gen Hosp, Taoyuan, Taiwan
[6] Share Hope Med Co Ltd, Taoyuan, Taiwan
关键词
Lean NAFLD; SNPs; PNPLA3; SAMM50; HAVO database; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY; EPIDEMIOLOGY; METAANALYSIS; PREVALENCE; SEVERITY; GENE;
D O I
10.1016/j.aohep.2024.101761
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction and Objectives: Lean adults with nonalcoholic fatty liver disease (NAFLD) have a higher risk of metabolic syndrome than lean controls. The study aimed to investigate the clinical and genetic features of lean NAFLD which remain unclear in Asian populations. Materials and Methods: This was a genetic cohort study conducted in the HAVO Health Exam Clinic in 2020 -2021 in Taiwan. Adults with a body mass index less than 24 kg/m2 were enrolled. Fatty liver was defined by ultrasonography. The candidate gene approach was based on the library of the NHGRI-EBI website. After removing duplication and nonsignificant variants, rs738409 in the PNPLA3 gene and rs3761472 in the SAMM50 gene were chosen. Multiple logistic regression models and receiver operating characteristic (ROC) curves were used. Results: A total of 1652 lean controls and 602 lean NAFLD patients were enrolled. The average age was 43.8 11.5 years. Lean NAFLD subjects were older and had a higher percentage of metabolic syndrome (case vs. control: 10.5 % vs. 1.5 %). The GG genotypes of PNPLA3 rs12483959 (OR: 3.06; 95% CI: 2.15-4.37) and SAMM50 rs3761472 (OR: 2.90; 95% CI: 2.04-4.14) had a higher risk of fatty liver after adjusting for BMI and metabolic syndrome. The areas under the ROC curve for PNPLA3 rs738409 and SAMM50 rs3761472 in the detection of lean NAFLD were 0.859 (95%CI: 0.841, 0.877) and 0.860 (95%CI: 0.843, 0.877), respectively. Conclusions: PNPLA3 rs738409 and SAMM50 rs3761472 gene polymorphisms are associated with a higher risk of fatty liver in lean individuals independent of BMI and metabolic syndrome in Asian populations. (c) 2024 Fundaci & oacute;n Cl & iacute;nica M & eacute;dica Sur, A.C. Published by Elsevier Espa & ntilde;a, S.L.U. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
引用
收藏
页数:6
相关论文
共 50 条
  • [21] STEATOTIC LIVER DISEASE IN LEAN PATIENTS IS ASSOCIATED WITH DIABETES, BUT NOT PNPLA3
    Espinoza, Angela Sato
    Chotiprasidhi, Perapa
    Wangensteen, Kirk
    HEPATOLOGY, 2024, 80 : S1930 - S1931
  • [22] More Evidence for the Genetic Susceptibility of Mexican Population to Nonalcoholic Fatty Liver Disease through PNPLA3
    Chinchilla-Lopez, Paulina
    Ramirez-Perez, Oscar
    Cruz-Ramon, Vania
    Canizales-Quinteros, Samuel
    Dominguez-Lopez, Aaron
    Ponciano-Rodriguez, Guadalupe
    Sanchez-Munoz, Fausto
    Mendez-Sanchez, Nahum
    ANNALS OF HEPATOLOGY, 2018, 17 (02) : 250 - 255
  • [23] Genetic Variants in the PNPLA3 Gene Are Associated with Nonalcoholic Steatohepatitis
    Islek, Eylul Ece
    Sazci, Ali
    Ozel, Mavi Deniz
    Aygun, Cem
    GENETIC TESTING AND MOLECULAR BIOMARKERS, 2014, 18 (07) : 489 - 496
  • [24] The PNPLA3 I148M polymorphismis associated with insulin resistance and nonalcoholic fatty liver disease in a normoglycaemic population
    Wang, Chih-Wen
    Lin, Hsing-Yi
    Shin, Shyi-Jang
    Yu, Ming-Lung
    Lin, Zu-Yau
    Dai, Chia-Yen
    Huang, Jee-Fu
    Chen, Shinn-Cherng
    Li, Steven Shoei-Lung
    Chuang, Wan-Long
    LIVER INTERNATIONAL, 2011, 31 (09) : 1326 - 1331
  • [25] Genetic variants in COL13A1, ADIPOQ and SAMM50, in addition to the PNPLA3 gene, confer susceptibility to elevated transaminase levels in an admixed Mexican population
    Larrieta-Carrasco, Elena
    Flores, Yvonne N.
    Macias-Kauffer, Luis R.
    Ramirez-Palacios, Paula
    Quiterio, Manuel
    Ramirez-Salazar, Eric G.
    Leon-Mimila, Paola
    Rivera-Paredez, Berenice
    Cabrera-Alvarez, Guillermo
    Canizales-Quinteros, Samuel
    Zhang, Zuo-Feng
    Lopez-Perez, Tania V.
    Salmeron, Jorge
    Velazquez-Cruz, Rafael
    EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2018, 104 (01) : 50 - 58
  • [26] Toward Genetic Prediction of Nonalcoholic Fatty Liver Disease Trajectories: PNPLA3 and Beyond
    Krawczyk, Marcin
    Liebe, Roman
    Lammert, Frank
    GASTROENTEROLOGY, 2020, 158 (07) : 1865 - +
  • [27] PNPLA3, the triacylglycerol synthesis/hydrolysis/storage dilemma, and nonalcoholic fatty liver disease
    Sookoian, Silvia
    Pirola, Carlos J.
    WORLD JOURNAL OF GASTROENTEROLOGY, 2012, 18 (42) : 6018 - 6026
  • [28] PNPLA3,the triacylglycerol synthesis/hydrolysis/storage dilemma,and nonalcoholic fatty liver disease
    Silvia Sookoian
    Carlos J Pirola
    World Journal of Gastroenterology, 2012, 18 (42) : 6018 - 6026
  • [29] Gut Microbiota and PNPLA3 RS738409 Associated with Nonalcoholic Fatty Liver Disease in Obese Youth
    Kravetz, Ayesha Monga
    Testerman, Todd
    Galuppo, Brittany
    Graf, Joerg
    Siebel, Stephan
    Feinn, Richard
    Santoro, Nicola
    DIABETES, 2020, 69
  • [30] Mitochondrial haplogroup G is associated with nonalcoholic fatty liver disease, while haplogroup A mitigates the effects of PNPLA3
    Gusdon, Aaron M.
    Hui, You
    Chen, Jing
    Mathews, Clayton E.
    Qu, Shen
    ENDOCRINOLOGY DIABETES & METABOLISM, 2021, 4 (01)