TY - JOUR
T1 - A PRISMA-compliant meta-Analysis of apolipoprotein C3 polymorphisms and nonalcoholic fatty liver disease
AU - Chen, Bing Fang
AU - Chien, Yueh
AU - Tsai, Pin Hsing
AU - Perng, Pang Chung
AU - Yang, Yi Ping
AU - Hsueh, Kuan Chun
AU - Liu, Chia Hung
AU - Wang, Yuan Hung
N1 - Funding Information:
This work was supported by Shuang Ho Hospital [grant number106TMU-SHH-25] and Taipei Medical University, Taiwan [grant number TMU103-AE1-B08].
Publisher Copyright:
© 2021 Wolters Kluwer Health. All rights reserved.
PY - 2021/10
Y1 - 2021/10
N2 - Background: The relationship between apolipoprotein C3 (APOC3) gene polymorphisms and nonalcoholic fatty liver disease (NAFLD) risk has been investigated in many studies, with inconclusive findings. This meta-Analysis evaluated the effect of APOC3 promoter region polymorphisms (-455T/C and-482C/T) on NAFLD susceptibility. Methods: A comprehensive search of eligible studies up to October 2020 was performed on Medline, Embase, Web of Science, and Google Scholar databases. No restriction was imposed on language, publication date, or publication status. Odds ratios (ORs) with their 95% confidence intervals (CIs) were calculated to assess the combined effect sizes. The levels of heterogeneity, sensitivity, subgroup, and publication bias were analyzed subsequently. Results: This meta-Analysis included eight studies, consisting of 1,511 patients with NAFLD and 1,900 controls fulfilling the inclusion criteria and exclusion criteria. The pooled analysis showed significant associations between APOC3-455T/C polymorphism and NAFLD risk in allelic (OR = 1.33; 95% CI = 1.05-1.67), dominant (OR = 1.34; 95% CI = 1.04-1.72), and recessive (OR = 1.60; 95% CI = 1.06-2.40) models. Ethnicity-based stratification showed that-455T/C polymorphism was significantly associated with NAFLD risk in the non-Asian but not in the Asian population. No association was evident between-482C/T polymorphism and NAFLD risk. Conclusion: Our findings suggest that APOC3 promoter region polymorphism-455T/C may be associated with NAFLD risk in the non-Asian but not in the Asian population. Additional studies with other functional polymorphisms are needed to discover APOC3 gene effects on NAFLD.
AB - Background: The relationship between apolipoprotein C3 (APOC3) gene polymorphisms and nonalcoholic fatty liver disease (NAFLD) risk has been investigated in many studies, with inconclusive findings. This meta-Analysis evaluated the effect of APOC3 promoter region polymorphisms (-455T/C and-482C/T) on NAFLD susceptibility. Methods: A comprehensive search of eligible studies up to October 2020 was performed on Medline, Embase, Web of Science, and Google Scholar databases. No restriction was imposed on language, publication date, or publication status. Odds ratios (ORs) with their 95% confidence intervals (CIs) were calculated to assess the combined effect sizes. The levels of heterogeneity, sensitivity, subgroup, and publication bias were analyzed subsequently. Results: This meta-Analysis included eight studies, consisting of 1,511 patients with NAFLD and 1,900 controls fulfilling the inclusion criteria and exclusion criteria. The pooled analysis showed significant associations between APOC3-455T/C polymorphism and NAFLD risk in allelic (OR = 1.33; 95% CI = 1.05-1.67), dominant (OR = 1.34; 95% CI = 1.04-1.72), and recessive (OR = 1.60; 95% CI = 1.06-2.40) models. Ethnicity-based stratification showed that-455T/C polymorphism was significantly associated with NAFLD risk in the non-Asian but not in the Asian population. No association was evident between-482C/T polymorphism and NAFLD risk. Conclusion: Our findings suggest that APOC3 promoter region polymorphism-455T/C may be associated with NAFLD risk in the non-Asian but not in the Asian population. Additional studies with other functional polymorphisms are needed to discover APOC3 gene effects on NAFLD.
KW - Apolipoprotein C3
KW - Meta-Analysis
KW - Nonalcoholic fatty liver disease
KW - Polymorphism
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U2 - 10.1097/JCMA.0000000000000564
DO - 10.1097/JCMA.0000000000000564
M3 - Article
C2 - 34108427
AN - SCOPUS:85118283489
SN - 1726-4901
VL - 84
SP - 923
EP - 929
JO - Journal of the Chinese Medical Association
JF - Journal of the Chinese Medical Association
IS - 10
ER -