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Editorial

Clustering of cardiometabolic risk factors in sub-Saharan Africans

Clustering of cardiometabolic risk factors in sub-Saharan Africans

Jean Jacques Noubiap1,&

 

1Centre for Heart Rhythm Disorders, University of Adelaide and Royal Adelaide Hospital, Adelaide, Australia

 

 

&Corresponding author
Jean Jacques Noubiap, Centre for Heart Rhythm Disorders, University of Adelaide and Royal Adelaide Hospital, Adelaide, Australia

 

 

Editorial    Down

Dyslipidemia, defined as abnormalities in circulating concentrations of total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, and triglycerides [1], is a major risk factor for cardiovascular disease (CVD). It is associated with heightened risk of stroke, myocardial infarction, and is a major contributor to global disability and mortality. According to the global burden of disease study, in 2019, high LDL cholesterol caused 4.4 million deaths (7.8% of total deaths) and 98.6 million disability-adjusted life-years (DALYs) (3.9% of total DALYs) globally, representing the fifth and eighth risk factor for mortality and disability, respectively [2].

Sub-Saharan Africa is one of the regions with the sharpest increase in the burden of CVD [3]. It is estimated that CVD will overtake infectious diseases as the leading cause of death by 2030 in the region [4]. This epidemiological transition is driven by high rates of undiagnosed and uncontrolled cardiometabolic risk factors such as hypertension, diabetes, obesity and dyslipidemia [4]. Until recently, the burden of dyslipidemia had remained largely neglected in sub-Saharan Africa. A systematic review and meta-analysis published two years ago provided the first comprehensive estimates of dyslipidemia prevalence among adults living in Africa based on data from 181 studies involving 309,207 individuals [5]. In the general population, the prevalence of dyslipidemia was 37.4% for low HDL cholesterol (< 1.0 mmol/L), 28.6% for high LDL cholesterol (≥ 3.3 mmol/L), 25.5% for high total cholesterol (≥ 5.2 mmol/L), and 17.0% for high triglyceride (≥ 1.7 mmol/L). In people with diabetes and hypertension, the prevalence was respectively 42.1% and 39.4% for low HDL cholesterol, 50.1% and 32.7% for high LDL cholesterol, 34.4% and 38.0% for high total cholesterol, and 35.5% and 22.2% for high triglyceride [5].

The study by Fausto Ciccacci and colleagues published in this volume of the Pan African Medical Journal represents a relevant contribution to the epidemiology of dyslipidemia in Africa, and specifically in Mozambique [6]. The authors estimated the prevalence of high total cholesterol (≥ 5.2 mmol/L) in a group of 885 patients with hypertension, diabetes or both, recruited in an urban health facility in Maputo, Mozambique. They found that high total cholesterol was present in 46.3% of the total population, 46.9% of patients with hypertension, 36.7% of those with diabetes, and 52.8% of those with both hypertension and diabetes. Furthermore, high total cholesterol was associated with female sex (77% increased risk) and a body mass index ≥ 25 kg/m2 (50% increased risk) [6].

The high prevalence rates of dyslipidemia in patients with hypertension and diabetes found in this study and in other clinical settings in sub-Saharan Africa have important implications [5]. Dyslipidemia should systematically be investigated as part of the comprehensive cardiovascular risk assessment of patients with hypertension and diabetes, and treated appropriately. This is crucial, considering the impact of dyslipidemia on atherosclerotic CVD in sub-Saharan African populations. For instance, in the large Stroke Investigative Research and Educational Network (SIREN) study conducted in Nigeria and Ghana, dyslipidemia had the second greatest population attributable risk for stroke (36%) after hypertension [7]. Definitive evidence exists that effective treatment of dyslipidemia, with statins for instance, markedly reduces CVD morbidity and premature mortality [8]. Unfortunately, studies have shown that in sub-Saharan African settings, the prescription and the use of statins are low among patients who need it, such as patients with hypertension, diabetes, or established CVD [9,10]. For example, a study in Ghana revealed that only 1 in 6 individuals with type 2 diabetes without CVD and 1 in 7 stroke survivors were prescribed statins [9]. Another study in South Africa showed that 1 in 2 patients on lipid lowering medications did not reach target LDL cholesterol levels [11], mainly due to underdosing [12]. Improved prescription and access to statin and other preventive medications for CVD risk reduction is urgently needed in these settings.

The Prospective Urban Rural Epidemiology (PURE) study has shown that preventive medications including aspirin, β blockers, angiotensin-converting enzyme inhibitors, and statins are unavailable and unaffordable for a large proportion of communities and households in low-income countries [13], and that lower availability and affordability of such essential CVD medications are associated with higher risk of major adverse cardiovascular events and mortality [14]. To curb the rising burden of CVD in sub-Saharan Africa, governments and health organizations should devote special efforts to scaling up access to essential CVD medications using key interventions such as differential pricing, bulk purchasing, and use of low-cost generics. Additional measures include training healthcare providers on primary and secondary prevention recommendations through academic detailing, formularies and guidelines, and task shifting from physicians to nurses.

Because hypertension and dyslipidemia frequently co-exist [5], a fixed-dose combination therapy (polypill strategy) has been proposed as an approach to reduce the burden of CVD, especially in low-income and middle-income countries. Indeed, the effectiveness of polypills comprising statins, multiple blood pressure-lowering medications, with or without aspirin for primary and secondary prevention of CVD was demonstrated in some recent large randomized controlled trials [15-17]. Polypills were also shown to be associated with high medication adherence and low number of adverse events [15]. Interestingly, a modeling study showed that polypill would be cost-effective compared with current care for secondary prevention of atherosclerotic CVD in China, India, Mexico, Nigeria, and South Africa [18].

Finally, despite an increasing attention to dyslipidemia in sub-Saharan Africa in the recent years, there is still a huge knowledge gap regarding the determinants and adverse effects of this complex condition in the region. Efforts are particularly needed to expand our knowledge on the molecular basis of dyslipidemias in Africans [19]. Large-scale population studies are needed at national and regional levels to better understand the complex interplay between genetic, behavioral, environmental, social and cardiometabolic risk factors including dyslipidemia and their impact on cardiovascular health outcomes. Collaborative efforts such as the AWI-Gen and SIREN studies within the Cardiovascular Working Group of the Human Heredity and Health in Africa (H3Africa) Consortium should be multiplied on the continent [20,21].

 

Disclosures: Dr Noubiap is supported by a Postgraduate Scholarship from the University of Adelaide.

 

 

Competing interests Up    Down

The author declares no competing interests.

 

 

Authors' contribution Up    Down

The author has read and agreed to the final manuscript.

 

 

References Up    Down

  1. Stone NJ, Robinson JG, Lichtenstein AH, Bairey Merz CN, Blum CB, Eckel RH et al. 2013 ACC/AHA guideline on the treatment of blood cholesterol to reduce atherosclerotic cardiovascular risk in adults: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol 2014;63(25 Pt B):2889-934. Google Scholar

  2. Murray CJL, Aravkin AY, Zheng P, Abbafati C, Abbas KM, Abbasi-Kangevari M et al. Global burden of 87 risk factors in 204 countries and territories, 1990-2019: a systematic analysis for the global burden of disease Study 2019. Lancet. 2020;396(10258):1223-1249. Google Scholar

  3. Vos T, Lim SS, Abbafati C, Abbas KM, Abbasi M, Abbasifard M et al. Global burden of 369 diseases and injuries in 204 countries and territories, 1990-2019: a systematic analysis for the global burden of disease study 2019. Lancet. 2020;396(10258):1204-1222. Google Scholar

  4. World Health Organization. Global status report on noncommunicable diseases 2014 Geneva: World Health Organization. 2014. Google Scholar

  5. Noubiap JJ, Bigna JJ, Nansseu JR, Nyaga UF, Balti EV, Echouffo-Tcheugui JB et al. Prevalence of dyslipidaemia among adults in Africa: a systematic review and meta-analysis. Lancet Glob Health. 2018;6(9):e998-e1007. PubMed | Google Scholar

  6. Ciccacci F, Majid N, Petrolati S, Agy M, Massango C, Orlando S et al. Hypercholesterolemia and related risk factors in a cohort of patients with diabetes and hypertension in Maputo, Mozambique. Pan Afr Med J. 2021;38:102.

  7. Owolabi MO, Sarfo F, Akinyemi R, Gebregziabher M, Akpa O, Akpalu A et al. Dominant modifiable risk factors for stroke in Ghana and Nigeria (SIREN): a case-control study. Lancet Glob Health. 2018;6(4):e436-e446. PubMed | Google Scholar

  8. Baigent C, Blackwell L, Emberson J, Holland LE, Reith C, Bhala N et al. Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170,000 participants in 26 randomised trials. Lancet. 2010;376(9753):1670-81. PubMed | Google Scholar

  9. Sarfo FS, Ovbiagele B. Prevalence and predictors of statin utilization among patient populations at high vascular risk in Ghana. J Neurol Sci. 2020;414:116838. PubMed | Google Scholar

  10. Mwita JC, Godman B, Esterhuizen TM. Statin prescription among patients with type 2 diabetes in Botswana: findings and implications. BMC Endocr Disord. 2020;20(1):36. PubMed | Google Scholar

  11. Rapeport N, Schamroth CL, Blom DJ. Gender and ethnic differences in the control of hyperlipidaemia and other vascular risk factors: insights from the Centralised Pan-South African survey on tHE Under-treatment of hypercholeSterolaemia (CEPHEUS SA) study. Cardiovasc J Afr. 2013;24(6):238-42. PubMed | Google Scholar

  12. Godman B, Bishop I, Campbell SM, Malmström RE, Truter I. Quality and efficiency of statin prescribing across countries with a special focus on South Africa: findings and future implications. Expert Rev Pharmacoecon Outcomes Res. 2015;15(2):323-30. PubMed | Google Scholar

  13. Khatib R, McKee M, Shannon H, Chow C, Rangarajan S, Teo K et al. Availability and affordability of cardiovascular disease medicines and their effect on use in high-income, middle-income, and low-income countries: an analysis of the PURE study data. Lancet 2016;387(10013):61-9. PubMed | Google Scholar

  14. Chow CK, Nguyen TN, Marschner S, Diaz R, Rahman O, Avezum A et al. Availability and affordability of medicines and cardiovascular outcomes in 21 high-income, middle-income and low-income countries. BMJ Glob Health. 2020 Nov;5(11):e002640. PubMed | Google Scholar

  15. Roshandel G, Khoshnia M, Poustchi H, Hemming K, Kamangar F, Gharavi A et al. Effectiveness of polypill for primary and secondary prevention of cardiovascular diseases (polyIran): a pragmatic, cluster-randomised trial. Lancet 2019;394(10199):672-683. PubMed | Google Scholar

  16. Muñoz D, Uzoije P, Reynolds C, Miller R, Walkley D, Pappalardo S et al. Polypill for Cardiovascular Disease Prevention in an Underserved Population. New England Journal of Medicine. 2019;381(12):1114-1123. Google Scholar

  17. Yusuf S, Joseph P, Dans A, Gao P, Teo K, Xavier D et al. Polypill with or without aspirin in persons without cardiovascular disease. N Engl J Med. 2021 Jan 21;384(3):216-228. PubMed | Google Scholar

  18. Lin JK, Moran AE, Bibbins-Domingo K, Falase B, Pedroza Tobias A, Mandke CN et al. Cost-effectiveness of a fixed-dose combination pill for secondary prevention of cardiovascular disease in China, India, Mexico, Nigeria, and South Africa: a modelling study. Lancet Glob Health. 2019;7(10):e1346-e1358. PubMed | Google Scholar

  19. Noubiap JJ, Mato EPM, Guewo-Fokeng M, Kaze AD, Boulenouar H, Wonkam A. Genetic determinants of dyslipidemia in African-based populations: a systematic review. OMICS. 2018;22(12):749-758. PubMed | Google Scholar

  20. Sarfo FS. Dyslipidaemia among African adults. Lancet Glob Health 2018;6(9):e940-e941. PubMed | Google Scholar

  21. Peprah E, Wiley K, Troyer J, Adebamowo SN, Adu D, Mayosi BM et al. Building a Platform to Enable NCD Research to Address Population Health in Africa: CVD Working Group Discussion at the Sixth H3Africa Consortium Meeting in Zambia. Glob Heart. 2016;11(1):165-70. PubMed | Google Scholar