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

被引:29
作者
Mengesha, Hayelom Gebrekirstos [1 ]
Petrucka, Pammla [2 ,3 ]
Spence, Cara [4 ]
Tafesse, Tadesse Bekele [5 ]
机构
[1] Adigrat Univ, Dept Pharm, Coll Med & Hlth Sci, Adigrat, Ethiopia
[2] Univ Saskatchewan, Coll Nursing, Saskatoon, SK, Canada
[3] Nelson Mandela African Inst Sci & Technol, Arusha, Tanzania
[4] Univ Saskatchewan, Int Off, Saskatoon, SK, Canada
[5] Haramaya Univ, Sch Pharm, Coll Hlth & Med Sci, Harar, Ethiopia
关键词
GENOME-WIDE ASSOCIATION; BLOOD-PRESSURE TRAITS; INSERTION/DELETION POLYMORPHISM;
D O I
10.1371/journal.pone.0211054
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:11
相关论文
共 31 条
[1]   Shifting trends in the pharmacologic treatment of hypertension in a Nigerian tertiary hospital: a real-world evaluation of the efficacy, safety, rationality and pharmaco-economics of old and newer anti hypertensive drugs [J].
Adigun, AQ ;
Ishola, DA ;
Akintomide, AO ;
Ajayi, AAL .
JOURNAL OF HUMAN HYPERTENSION, 2003, 17 (04) :277-285
[2]  
Arfa Imen, 2010, Tunis Med, V88, P38
[3]   Pharmacogenetic association of the angiotensin-converting enzyme insertion/deletion polymorphism on blood pressure and cardiovascular risk in relation to antihypertensive treatment - The genetics of hypertension-associated treatment (GenHAT) study [J].
Arnett, DK ;
Davis, BR ;
Ford, CE ;
Boerwinkle, E ;
Leiendecker-Foster, C ;
Miller, MB ;
Black, H ;
Eckfeldt, JH .
CIRCULATION, 2005, 111 (25) :3374-3383
[4]   Why do hypertensive patients of African ancestry respond better to calcium blockers and diuretics than to ACE inhibitors and β-adrenergic blockers? A systematic review [J].
Brewster, Lizzy M. ;
Seedat, Yackoob K. .
BMC MEDICINE, 2013, 11
[5]   Systematic review: Antihypertensive drug therapy in black patients [J].
Brewster, LM ;
van Montfrans, GA ;
Kleijnen, J .
ANNALS OF INTERNAL MEDICINE, 2004, 141 (08) :614-627
[6]   Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls [J].
Burton, Paul R. ;
Clayton, David G. ;
Cardon, Lon R. ;
Craddock, Nick ;
Deloukas, Panos ;
Duncanson, Audrey ;
Kwiatkowski, Dominic P. ;
McCarthy, Mark I. ;
Ouwehand, Willem H. ;
Samani, Nilesh J. ;
Todd, John A. ;
Donnelly, Peter ;
Barrett, Jeffrey C. ;
Davison, Dan ;
Easton, Doug ;
Evans, David ;
Leung, Hin-Tak ;
Marchini, Jonathan L. ;
Morris, Andrew P. ;
Spencer, Chris C. A. ;
Tobin, Martin D. ;
Attwood, Antony P. ;
Boorman, James P. ;
Cant, Barbara ;
Everson, Ursula ;
Hussey, Judith M. ;
Jolley, Jennifer D. ;
Knight, Alexandra S. ;
Koch, Kerstin ;
Meech, Elizabeth ;
Nutland, Sarah ;
Prowse, Christopher V. ;
Stevens, Helen E. ;
Taylor, Niall C. ;
Walters, Graham R. ;
Walker, Neil M. ;
Watkins, Nicholas A. ;
Winzer, Thilo ;
Jones, Richard W. ;
McArdle, Wendy L. ;
Ring, Susan M. ;
Strachan, David P. ;
Pembrey, Marcus ;
Breen, Gerome ;
St Clair, David ;
Caesar, Sian ;
Gordon-Smith, Katherine ;
Jones, Lisa ;
Fraser, Christine ;
Green, Elain K. .
NATURE, 2007, 447 (7145) :661-678
[7]  
Dame han T, 2015, RENIN ANGIOTENSIN SY
[8]   Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk [J].
Ehret, Georg B. ;
Munroe, Patricia B. ;
Rice, Kenneth M. ;
Bochud, Murielle ;
Johnson, Andrew D. ;
Chasman, Daniel I. ;
Smith, Albert V. ;
Tobin, Martin D. ;
Verwoert, Germaine C. ;
Hwang, Shih-Jen ;
Pihur, Vasyl ;
Vollenweider, Peter ;
O'Reilly, Paul F. ;
Amin, Najaf ;
Bragg-Gresham, Jennifer L. ;
Teumer, Alexander ;
Glazer, Nicole L. ;
Launer, Lenore ;
Zhao, Jing Hua ;
Aulchenko, Yurii ;
Heath, Simon ;
Sober, Siim ;
Parsa, Afshin ;
Luan, Jian'an ;
Arora, Pankaj ;
Dehghan, Abbas ;
Zhang, Feng ;
Lucas, Gavin ;
Hicks, Andrew A. ;
Jackson, Anne U. ;
Peden, John F. ;
Tanaka, Toshiko ;
Wild, Sarah H. ;
Rudan, Igor ;
Igl, Wilmar ;
Milaneschi, Yuri ;
Parker, Alex N. ;
Fava, Cristiano ;
Chambers, John C. ;
Fox, Ervin R. ;
Kumari, Meena ;
Go, Min Jin ;
van der Harst, Pim ;
Kao, Wen Hong Linda ;
Sjogren, Marketa ;
Vinay, D. G. ;
Alexander, Myriam ;
Tabara, Yasuharu ;
Shaw-Hawkins, Sue ;
Whincup, Peter H. .
NATURE, 2011, 478 (7367) :103-109
[9]   Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations [J].
Franceschini, Nora ;
Fox, Ervin ;
Zhang, Zhaogong ;
Edwards, Todd L. ;
Nalls, Michael A. ;
Sung, Yun Ju ;
Tayo, Bamidele O. ;
Sun, Yan V. ;
Gottesman, Omri ;
Adeyemo, Adebawole ;
Johnson, Andrew D. ;
Young, J. Hunter ;
Rice, Ken ;
Duan, Qing ;
Chen, Fang ;
Li, Yun ;
Tang, Hua ;
Fornage, Myriam ;
Keene, Keith L. ;
Andrews, Jeanette S. ;
Smith, Jennifer A. ;
Fau, Jessica D. ;
Guangfa, Zhang ;
Guo, Wei ;
Liu, Yu ;
Murray, Sarah S. ;
Musani, Solomon K. ;
Srinivasan, Sathanur ;
Edwards, Digna R. Velez ;
Wang, Heming ;
Becker, Lewis C. ;
Bovet, Pascal ;
Bochud, Murielle ;
Broecke, Ulrich ;
Burnier, Michel ;
Carty, Cara ;
Chasman, Daniel I. ;
Ehret, Georg ;
Chen, Wei-Min ;
Chen, Guanjie ;
Chen, Wei ;
Ding, Jingzhong ;
Dreisbach, Albert W. ;
Evans, Michele K. ;
Guo, Xiuqing ;
Garcia, Melissa E. ;
Jensen, Rich ;
Keller, Margaux E. ;
Lettre, Guillaume ;
Lotay, Vaneet .
AMERICAN JOURNAL OF HUMAN GENETICS, 2013, 93 (03) :545-554
[10]   Angiotensin I converting enzyme gene polymorphism in Chinese patients with hypertension [J].
Jeng, JR ;
Harn, HJ ;
Jeng, CY ;
Yueh, KC ;
Shieh, SM .
AMERICAN JOURNAL OF HYPERTENSION, 1997, 10 (05) :558-561