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血管紧张素转化酶基因多态性对非洲高血压的影响:Meta 分析和系统评价。

Effects of angiotensin converting enzyme gene polymorphism on hypertension in Africa: A meta-analysis and systematic review.

机构信息

Department of Pharmacy, College of Medicine and Health Sciences, Adigrat University, Adigrat, Ethiopia.

University of Saskatchewan, College of Nursing, Saskatoon, SK, Canada, Adjunct Nelson Mandela African Institute of Science and Technology, Arusha, Tanzania.

出版信息

PLoS One. 2019 Feb 14;14(2):e0211054. doi: 10.1371/journal.pone.0211054. eCollection 2019.

Abstract

BACKGROUND

Hypertension is dramatically increasing in Africa with evidence of increased severity and resistance to treatment. Although angiotensin converting enzyme gene polymorphism is associated with higher prevalence of hypertension, the evidence is inconclusive on its influence on the emerging pattern in Africa. This meta-analysis is conducted to pool the available evidence to inform future research and interventions.

METHODS

Articles published through May 2018 were systematically searched in PubMed, Scopus and EMBASE databases. Studies were assessed for inclusion by two independent researchers. Six models were used to assess the effect of angiotensin converting enzyme deletion-insertion gene polymorphism. Heterogeneity and publication bias were tested and sensitivity analysis was carried out. Odds ratio and 95% confidence intervals were measured for pooled effect. Both random effect and fixed effect models were used, whilst the frequency of DD, II and DI genotypes were computed and compared.

RESULT

Patients with D allele were 1.49 times more likely to develop essential hypertension compared with patients who carry the I allele (OR:1.49; CI:1.07, 2.07). Similarly, patients who had homozygous co-dominance genotype DD (i.e., DD vs II) were at a 2.17 times higher risk of essential hypertension compared to the co-dominant genotype II (OR:2.17, CI:1.79, 3.18), dominant model (I.e., DD+ID vs II) (OR:1.48; CI:1.03, 2.12), and recessive model (OR:1.64; CI:1.03, 2.61). On subgroup analysis, participants from Sub-Saharan Africa were more genetically susceptible to hypertension compared to their North Africa counterparts. There was no publication bias found, but there was high to moderate heterogeneity.

CONCLUSION

ACE I/D polymorphism is associated with essential hypertension in Africa in the allele contrast model, as well as the dominant, recessive and homozygous codominance model. On subgroup analysis, ACE I/D was associated with essential hypertension in patients from Sub-Saharan Africa but not in North Africa. A future large scale study, which includes different ethnic groups, is recommended.

摘要

背景

高血压在非洲急剧增加,其严重程度和治疗抵抗的证据也在增加。尽管血管紧张素转换酶基因多态性与高血压的高患病率有关,但关于其对非洲新兴模式的影响的证据尚无定论。进行这项荟萃分析是为了汇集现有证据,为未来的研究和干预提供信息。

方法

通过系统检索 PubMed、Scopus 和 EMBASE 数据库,检索截止到 2018 年 5 月发表的文章。由两名独立的研究人员评估纳入的研究。使用 6 种模型评估血管紧张素转换酶缺失插入基因多态性的影响。测试了异质性和发表偏倚,并进行了敏感性分析。测量了合并效应的比值比和 95%置信区间。同时使用随机效应和固定效应模型,计算并比较 DD、II 和 DI 基因型的频率。

结果

与携带 I 等位基因的患者相比,携带 D 等位基因的患者发生原发性高血压的可能性高 1.49 倍(OR:1.49;CI:1.07,2.07)。同样,具有纯合共显性基因型 DD(即 DD 与 II)的患者患原发性高血压的风险比共显性基因型 II 高 2.17 倍(OR:2.17,CI:1.79,3.18),显性模型(即 DD+ID 与 II)(OR:1.48;CI:1.03,2.12)和隐性模型(OR:1.64;CI:1.03,2.61)。亚组分析显示,与北非患者相比,来自撒哈拉以南非洲的参与者在遗传上更容易患高血压。未发现发表偏倚,但存在高至中度异质性。

结论

ACE I/D 多态性与非洲的原发性高血压相关,在等位基因对比模型以及显性、隐性和纯合共显性模型中均如此。在亚组分析中,ACE I/D 与撒哈拉以南非洲的原发性高血压患者相关,但与北非患者无关。建议进行一项包括不同种族群体的大规模未来研究。

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