The rs626283 variant in the MBOAT7 gene is associated with insulin resistance and fatty liver in Caucasian obese youth

Giuseppina R. Umano, Sonia Caprio, Anna Di Sessa, Naga Chalasani, Daniel J. Dykas, Bridget Pierpont, Allen E. Bale, Nicola Santoro

Research output: Contribution to journalArticle

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Abstract

OBJECTIVES: Non alcoholic fatty liver disease (NAFLD) is a leading cause of liver damage in childhood, its occurrence is infl uenced by genetic and environmental factors. Recently, the rs626283 polymorphism in the MBOAT7 gene has been found to be associated with alcoholic liver disease and NAFLD in adults. METHODS: In a multiethnic cohort of obese children and adolescents we genotyped the rs626283 polymorphism in the MBOAT7 gene, evaluated insulin sensitivity by an oral glucose tolerance test, and measured the intra-hepatic fat content (HFF%) by magnetic resonance imaging. RESULTS: In Caucasian youth, the minor allele (C) was associated with HFF% in (P =0.003), fasting insulin (P =0.03), area under the curve of glucose (P =0.03), and lower degree of whole-body insulin sensitivity (P =0.01) independent of age, gender, and body mass index z -score. A partial correlation showed that the association between the rs626283 variant and insulin resistance was driven by the presence of hepatic steatosis (P =0.009). However, there was no association between the rs626283 and hepatic steatosis among Hispanic and African American children and youth. The association between the rs626283 in the MBOAT7 gene among Caucasians was independent of the PNPLA3 rs738409, GCKR 1260326, and TM6SF2 rs58542926 (P =0.01). The four polymorphisms combined explained~19% of the HFF% in Caucasian obese children and adolescents. CONCLUSIONS: The rs626283 variant in the MBOAT7 gene is associated with NAFLD and may affect glucose metabolism by modulating intra-hepatic fat content in Caucasian obese children and adolescents.

Original languageEnglish (US)
Pages (from-to)376-383
Number of pages8
JournalAmerican Journal of Gastroenterology
Volume113
Issue number3
DOIs
StatePublished - Mar 1 2018

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Fatty Liver
Insulin Resistance
Liver
Genes
Fats
Glucose
Alcoholic Liver Diseases
Glucose Tolerance Test
Hispanic Americans
African Americans
Area Under Curve
Fasting
Body Mass Index
Alleles
Magnetic Resonance Imaging
Insulin
Non-alcoholic Fatty Liver Disease

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology

Cite this

The rs626283 variant in the MBOAT7 gene is associated with insulin resistance and fatty liver in Caucasian obese youth. / Umano, Giuseppina R.; Caprio, Sonia; Di Sessa, Anna; Chalasani, Naga; Dykas, Daniel J.; Pierpont, Bridget; Bale, Allen E.; Santoro, Nicola.

In: American Journal of Gastroenterology, Vol. 113, No. 3, 01.03.2018, p. 376-383.

Research output: Contribution to journalArticle

Umano, Giuseppina R. ; Caprio, Sonia ; Di Sessa, Anna ; Chalasani, Naga ; Dykas, Daniel J. ; Pierpont, Bridget ; Bale, Allen E. ; Santoro, Nicola. / The rs626283 variant in the MBOAT7 gene is associated with insulin resistance and fatty liver in Caucasian obese youth. In: American Journal of Gastroenterology. 2018 ; Vol. 113, No. 3. pp. 376-383.
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abstract = "OBJECTIVES: Non alcoholic fatty liver disease (NAFLD) is a leading cause of liver damage in childhood, its occurrence is infl uenced by genetic and environmental factors. Recently, the rs626283 polymorphism in the MBOAT7 gene has been found to be associated with alcoholic liver disease and NAFLD in adults. METHODS: In a multiethnic cohort of obese children and adolescents we genotyped the rs626283 polymorphism in the MBOAT7 gene, evaluated insulin sensitivity by an oral glucose tolerance test, and measured the intra-hepatic fat content (HFF{\%}) by magnetic resonance imaging. RESULTS: In Caucasian youth, the minor allele (C) was associated with HFF{\%} in (P =0.003), fasting insulin (P =0.03), area under the curve of glucose (P =0.03), and lower degree of whole-body insulin sensitivity (P =0.01) independent of age, gender, and body mass index z -score. A partial correlation showed that the association between the rs626283 variant and insulin resistance was driven by the presence of hepatic steatosis (P =0.009). However, there was no association between the rs626283 and hepatic steatosis among Hispanic and African American children and youth. The association between the rs626283 in the MBOAT7 gene among Caucasians was independent of the PNPLA3 rs738409, GCKR 1260326, and TM6SF2 rs58542926 (P =0.01). The four polymorphisms combined explained~19{\%} of the HFF{\%} in Caucasian obese children and adolescents. CONCLUSIONS: The rs626283 variant in the MBOAT7 gene is associated with NAFLD and may affect glucose metabolism by modulating intra-hepatic fat content in Caucasian obese children and adolescents.",
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T1 - The rs626283 variant in the MBOAT7 gene is associated with insulin resistance and fatty liver in Caucasian obese youth

AU - Umano, Giuseppina R.

AU - Caprio, Sonia

AU - Di Sessa, Anna

AU - Chalasani, Naga

AU - Dykas, Daniel J.

AU - Pierpont, Bridget

AU - Bale, Allen E.

AU - Santoro, Nicola

PY - 2018/3/1

Y1 - 2018/3/1

N2 - OBJECTIVES: Non alcoholic fatty liver disease (NAFLD) is a leading cause of liver damage in childhood, its occurrence is infl uenced by genetic and environmental factors. Recently, the rs626283 polymorphism in the MBOAT7 gene has been found to be associated with alcoholic liver disease and NAFLD in adults. METHODS: In a multiethnic cohort of obese children and adolescents we genotyped the rs626283 polymorphism in the MBOAT7 gene, evaluated insulin sensitivity by an oral glucose tolerance test, and measured the intra-hepatic fat content (HFF%) by magnetic resonance imaging. RESULTS: In Caucasian youth, the minor allele (C) was associated with HFF% in (P =0.003), fasting insulin (P =0.03), area under the curve of glucose (P =0.03), and lower degree of whole-body insulin sensitivity (P =0.01) independent of age, gender, and body mass index z -score. A partial correlation showed that the association between the rs626283 variant and insulin resistance was driven by the presence of hepatic steatosis (P =0.009). However, there was no association between the rs626283 and hepatic steatosis among Hispanic and African American children and youth. The association between the rs626283 in the MBOAT7 gene among Caucasians was independent of the PNPLA3 rs738409, GCKR 1260326, and TM6SF2 rs58542926 (P =0.01). The four polymorphisms combined explained~19% of the HFF% in Caucasian obese children and adolescents. CONCLUSIONS: The rs626283 variant in the MBOAT7 gene is associated with NAFLD and may affect glucose metabolism by modulating intra-hepatic fat content in Caucasian obese children and adolescents.

AB - OBJECTIVES: Non alcoholic fatty liver disease (NAFLD) is a leading cause of liver damage in childhood, its occurrence is infl uenced by genetic and environmental factors. Recently, the rs626283 polymorphism in the MBOAT7 gene has been found to be associated with alcoholic liver disease and NAFLD in adults. METHODS: In a multiethnic cohort of obese children and adolescents we genotyped the rs626283 polymorphism in the MBOAT7 gene, evaluated insulin sensitivity by an oral glucose tolerance test, and measured the intra-hepatic fat content (HFF%) by magnetic resonance imaging. RESULTS: In Caucasian youth, the minor allele (C) was associated with HFF% in (P =0.003), fasting insulin (P =0.03), area under the curve of glucose (P =0.03), and lower degree of whole-body insulin sensitivity (P =0.01) independent of age, gender, and body mass index z -score. A partial correlation showed that the association between the rs626283 variant and insulin resistance was driven by the presence of hepatic steatosis (P =0.009). However, there was no association between the rs626283 and hepatic steatosis among Hispanic and African American children and youth. The association between the rs626283 in the MBOAT7 gene among Caucasians was independent of the PNPLA3 rs738409, GCKR 1260326, and TM6SF2 rs58542926 (P =0.01). The four polymorphisms combined explained~19% of the HFF% in Caucasian obese children and adolescents. CONCLUSIONS: The rs626283 variant in the MBOAT7 gene is associated with NAFLD and may affect glucose metabolism by modulating intra-hepatic fat content in Caucasian obese children and adolescents.

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