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American Ancestry Is a Risk Factor for Suspected Nonalcoholic Fatty Liver Disease in Hispanic/Latino Adults.
Kallwitz, Eric R; Tayo, Bamidele O; Kuniholm, Mark H; Cai, Jianwen; Daviglus, Martha; Cooper, Richard S; Cotler, Scott J.
Afiliación
  • Kallwitz ER; Division of Hepatology, Loyola University Medical Center, Maywood, Illinois. Electronic address: ekallwitz@lumc.edu.
  • Tayo BO; Department of Public Health Sciences, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois.
  • Kuniholm MH; School of Public Health, SUNY at Albany, Albany, New York.
  • Cai J; UNC Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina.
  • Daviglus M; Institute for Minority Health Research, University of Illinois, Chicago, Illinois.
  • Cooper RS; Department of Public Health Sciences, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois.
  • Cotler SJ; Division of Hepatology, Loyola University Medical Center, Maywood, Illinois.
Clin Gastroenterol Hepatol ; 17(11): 2301-2309, 2019 10.
Article en En | MEDLINE | ID: mdl-30743004
BACKGROUND & AIMS: Nonalcoholic fatty liver disease (NAFLD) disproportionally affects Hispanic/Latino populations. However, the magnitude varies among Hispanic/Latino ethnic groups. We investigated the mechanisms of these disparities. METHODS: We examined associations of NAFLD-associated genetic variants and continental ancestry with suspected NAFLD, levels of alanine aminotransferase (ALT), and liver fibrosis using data from the Hispanic Community Health Study/Study of Latinos-a population-based study of Hispanic/Latino adults in the United States. We evaluated data from 16,415 Hispanic/Latino adults in 4 cities from 2008 through 2011. Subjects suspected of having NAFLD or liver fibrosis were identified based on unexplained increases in levels of aminotransferases and FIB-4 score, respectively. RESULTS: Among the 9342 participants with available genetic and aminotransferase data, the PNPLA3 G allele (odds ratio [OR], 1.53; 95% CI, 1.41-1.66), TM6SF2 T allele (OR, 1.41; 95% CI, 1.20-1.67), and PPP1R3B G allele (OR, 1.16; 95% CI, 1.06-1.28) were associated with suspected NAFLD. PNPLA3 G was also associated with increased levels of ALT, except in participants with Dominican and South American backgrounds, and with liver fibrosis. The frequency of PNPLA3 G was high (41%) and TM6SF2 T (5%) was low in Hispanic/Latinos. PNPLA3 G frequency differed among Hispanic background groups with the highest proportion in Mexicans (52%) and the lowest proportion in Dominicans (23%). After adjustment for demographic, clinical, and behavioral factors, as well as PNPLA3 G, TM6SF2 T, and PPP1R3B G, American ancestry had a positive association with level of ALT (r = 6.61%; P < .001), whereas African (r = -3.84%; P < .001) and European (r = -4.31%; P < .001) ancestry were inversely associated with level of ALT. CONCLUSIONS: American ancestry and PNPLA3 G are independent predictors of ALT levels in US Hispanic/Latinos and may in part explain NAFLD disparities in US Hispanic/Latinos.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hispánicos o Latinos / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Enfermedad del Hígado Graso no Alcohólico / Transaminasas / Lipasa / Proteínas de la Membrana Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Gastroenterol Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hispánicos o Latinos / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Enfermedad del Hígado Graso no Alcohólico / Transaminasas / Lipasa / Proteínas de la Membrana Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Gastroenterol Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2019 Tipo del documento: Article