The SA Journal Diabetes & Vascular Disease Vol 11 No 3 (September 2014) - page 36

130
VOLUME 11 NUMBER 3 • SEPTEMBER 2014
RESEARCH ARTICLE
SA JOURNAL OF DIABETES & VASCULAR DISEASE
cardiovascular disease who were participants of the Health, Aging,
and Body Composition study (Health ABC study), the presence of
major or minor ECG aberrations at baseline was associated with
coronary heart disease risk during follow up, independent of
classical cardiovascular risk factors.
15
The findings of the Health
ABC study suggest that the presence of ECG aberrations, including
those used to diagnose cardiac ischaemia in our study, should be
given consideration as they may indicate an adverse underlying
cardiovascular risk profile.
Approximately 13% of participants in this study were on a
statin, preventive treatment widely recommended for routine use
in people with diabetes. No correlation was found between statin
use and ECG-diagnosed ischaemic heart disease. This suggests that
the use of statins in this population could be almost doubled by
using ECG criteria to diagnose for ischaemic heart disease. It was
shown in a recent study that the use of recommended preventive
therapies for cardiovascular disease risk reduction, based on global
risk evaluation, was limited in Africa in people with diabetes and
those without.
16
Our study had some limitations. In the absence of follow up, we
were unable to establish any causal relationship between identified
predictors of cardiovascular risk and ECG aberrations. This was a
hospital-based study and therefore included participants who may
not have been typical of those in the community where the majority
of type 2 diabetes persons remain undiagnosed.
17
While this could
have affected the prevalence of ECG changes found in our study,
it was less likely to have affected the direction of associations
described, and therefore would not have invalidated the major
findings from this study.
That ECGs were interpreted by an investigator who was unaware
of the clinical background of the patients, which could have
affected the prevalence of some of the outcomes. Indeed, using
such an approach resulted at best in a description of significant
changes, with no assumption about possible correlations between
coincident aberrations in the same patient.
Our study had somemajor advantages, including the considerable
sample size, which gave us reasonable statistical power to reliably
investigate the parameters. We were also able to investigate the
full spectrum of resting ECG aberrations, which no previous study
has achieved in Africa. The extensive data collection of both clinical
and biological profiles enabled a wide range of predictors to be
investigated for their possible link with prevalent ECG aberrations.
Conclusion
ECG aberrations are frequent in people with diabetes in sub-Saharan
Africa. While some may be benign, others are indicators of serious
underlying conditions or high future risk for cardiovascular disease.
These aberrations have the potential to improve cardiovascular
disease risk stratification and the implementation of preventative
strategies in people with diabetes in sub-Saharan Africa.
The growing prevalence of serious ECG aberrations over time
suggests the need for strategies to monitor such changes and
their determinants, so as to refine the cardiovascular preventative
strategies in sub-Saharan Africa. Elsewhere, dedicated diabetes
registries have successfully served these functions.
References
1. International Diabetes Federation.
Diabetes Atlas
. 4th edn. Brussels: IDF, 2009.
2. International Task Force for Prevention of Coronary Heart Disease, International
Atherosclerosis Society.
Pocket Guide to Prevention of Coronary Heart Disease
.
Munster: Born Bruckmeier Verlag GmbH, 2003.
3. International Diabetes Federation.
Global Guidelines for Type 2 Diabetes
. Brussels:
International Diabetes Federation, 2005.
4. IDF Africa Region Task Force on Type 2 Diabetes Clinical Practice Guidelines. Type
2 clinical practice guidelines for sub-Saharan Africa: IDF Afro Region, 2006.
5. Choukem SP, Kengne AP, Dehayem YM, Simo NL, Mbanya JC. Hypertension in
people with diabetes in sub-Saharan Africa: revealing the hidden face of the
iceberg.
Diabetes Res Clin Pract
2007; 77: 293–299.
6. Kengne AP, Djouogo CF, Dehayem MY, Fezeu L, Sobngwi E, Lekoubou A,
et al
.
Admission trends over 8 years for diabetic foot ulceration in a specialized diabetes
unit in Cameroon.
Int J Low Extrem Wounds
2009;
8
: 180–186.
7. Norman JE, Jr., Levy D. Improved electrocardiographic detection of echocardio-
graphic left ventricular hypertrophy: results of a correlated data base approach.
J
Am Coll Cardiol
1995;
26
: 1022–1029.
8. Lutale JJ, Thordarson H, Gulam-Abbas Z, Vetvik K, Gerdts E. Prevalence and
covariates of electrocardiographic left ventricular hypertrophy in diabetic patients
in Tanzania.
Cardiovasc J Afr
2008;
19
: 8–14.
9. Lester FT, Keen H. Macrovascular disease in middle-aged diabetic patients in
Addis Ababa, Ethiopia.
Diabetologia
1988;
31
: 361–367.
10. Odusan O, Familoni OB, Raimi TH. Correlates of cardiac autonomic neuropathy
in Nigerian patients with type 2 diabetes mellitus.
Afr J Med Med Sci
2008;
37
:
315–-320.
11. Kengne AP, Amoah AG, Mbanya JC. Cardiovascular complications of diabetes
mellitus in sub-Saharan Africa.
Circulation
2005;
112
: 3592–3601.
12. Mbanya JC, Sobngwi E, Mbanya DS, Ngu KB. Left ventricular mass and systolic
function in African diabetic patients: association with microalbuminuria.
Diabetes
Metab
2001;
27
: 378–382.
13. Joubert J, McLean CA, Reid CM, Davel D, Pilloy W, Delport R,
et al
. Ischemic heart
disease in black South African stroke patients.
Stroke
2000;
31
: 1294–1298.
14. Brink AJ. The normal electrocardiogram in the adult South African Bantu.
S Afr J
Lab Clin Med
1956;
2
: 97–123.
15. Auer R, Bauer DC, Marques-Vidal P, Butler J, Min LJ, Cornuz J,
et al.
Association
of major and minor ECG abnormalities with coronary heart disease events.
J Am
Med Assoc
2012;
307
: 1497–1505.
16. Kengne AP, Njamnshi AK, Mbanya JC. Cardiovascular risk reduction in diabetes
in sub-Saharan Africa: What should the priorities be in the absence of global risk
evaluation tools?
Clin Med: Cardiol
2008;
2
: 25–31.
17. Mbanya JC, Kengne AP, Assah F. Diabetes care in Africa.
Lancet
2006;
368
: 1628–
1629.
1...,26,27,28,29,30,31,32,33,34,35 37,38,39,40,41,42,43,44
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