Literature DB >> 25083581

ApoB gene SpIns/Del, XbaI polymorphisms and myocardial infarction: a meta-analysis of 7169 participants.

Yan-yan Li1.   

Abstract

BACKGROUND: Apolipoprotein B (ApoB) gene signal peptide insertion/deletion (SpIns/Del, I/D) and XbaI polymorphisms have been associated with susceptibility to myocardial infarction (MI). However, the results of studies on this association are still controversial. OBJECTIVE AND METHODS: This study explored reports published from 1986 to 2008 regarding the association of ApoB gene SpIns/Del and XbaI polymorphisms with MI. A meta-analysis including 7169 participants from 19 individual studies was performed. The pooled odds ratios (ORs) and their corresponding 95% confidence intervals (95% CIs) were evaluated by fixed-effect or random-effect models.
RESULTS: A significant relationship between ApoB SpIns/Del gene polymorphism and MI was found under allelic (OR: 1.270, 95% CI: 1.090-1.480, P = 0.002), recessive (OR: 1.360, 95% CI: 1.130-1.630, P = 0.0009), dominant (OR: 1.091, 95% CI: 1.037-1.146, P = 0.001), homozygous (OR: 1.610, 95% CI: 1.330-1.950, P <0.00001) and heterozygous (OR: 1.081, 95% CI: 1.020-1.146, P = 0.009) genetic models. A marginal relationship between ApoB XbaI polymorphism and MI was found under a dominant genetic model (OR: 1.083, 95% CI: 1.004-1.168, P = 0.039). No significant association was detected under other genetic models (P >0.05). However, in the non-European subgroup analysis, increased MI risk emerged under all genetic models (P <0.05).
CONCLUSION: ApoB SpIns/Del gene polymorphism was positively associated with increased MI risk. D allele and DD genotype carriers might be predisposed to MI susceptibility. The ApoB XbaI gene polymorphism locus had a significant positive association with increased MI risk only in the non-European population. T allele and TT genotype carriers might be susceptible to MI in the non-European population. On the contrary, the ApoB gene XbaI restriction fragment length polymorphism was not associated with increased MI risk in the entire population, particularly in the European population.

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Year:  2014        PMID: 25083581     DOI: 10.2459/JCM.0b013e328364be64

Source DB:  PubMed          Journal:  J Cardiovasc Med (Hagerstown)        ISSN: 1558-2027            Impact factor:   2.160


  4 in total

1.  Associations of the APOB rs693 and rs17240441 polymorphisms with plasma APOB and lipid levels: a meta-analysis.

Authors:  Caiqin Niu; Zhi Luo; Liuqin Yu; Yang Yang; Yun Chen; Xin Luo; Feiya Lai; Yongyan Song
Journal:  Lipids Health Dis       Date:  2017-09-06       Impact factor: 3.876

2.  Deletion allele of Apo B gene is associated with higher inflammation, oxidative stress and dyslipidemia in obese type 2 diabetic patients: an analytical cross-sectional study.

Authors:  Nasim Mokhtary; Seyedeh Neda Mousavi; Gity Sotoudeh; Mostafa Qorbani; Maryam Dehghani; Fariba Koohdani
Journal:  BMC Endocr Disord       Date:  2022-03-22       Impact factor: 2.763

3.  Association between the APOB XbaI and EcoRI polymorphisms and lipids in Chinese: a meta-analysis.

Authors:  Wei Gu; Mingduo Zhang; Shaojun Wen
Journal:  Lipids Health Dis       Date:  2015-10-07       Impact factor: 3.876

4.  Distribution of polymorphism rs693 of ApoB gene in a sample of Colombian Caribbeans.

Authors:  Evelyn Mendoza-Torres; Nicole Samuel Pereira Sanandrés; José Luis Villarreal Camacho; Xilene Mendoza Sánchez; César De La Espriella Pérez; Lourdes Luz Varela Prieto; Daniel Antonio Villanueva Torregrosa
Journal:  Colomb Med (Cali)       Date:  2019-09-30
  4 in total

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