Electrocardiographic Left Ventricular Hypertrophy
Electrocardiographic Left Ventricular Hypertrophy
Electrocardiographic Left Ventricular Hypertrophy
net/publication/281499231
CITATIONS READS
8 35
7 authors, including:
Some of the authors of this publication are also working on these related projects:
All content following this page was uploaded by Modou Jobe on 18 January 2022.
DOI: http://dx.doi.org/10.4314/gmj.v49i1.4
Corresponding Author: Dr. M. Jobe E-mail: [email protected]
Conflict of Interest: None declared
SUMMARY INTRODUCTION
Background: The global prevalence of diabetes and its The global prevalence of diabetes mellitus (DM) con-
complications is increasing worldwide. Its role in coro- tinues to rise at an alarming rate.1 It is acknowledged as
nary heart disease has been linked with the presence of a principal risk factor for cardiovascular morbidity and
left ventricular hypertrophy (LVH). The present study mortality and has a heavy impact on the global health
aims to determine the prevalence of electrocardio- expenditure due to both its short and long term compli-
graphic left ventricular hypertrophy (ECG-LVH) in cations.2 DM is closely linked to coronary events3 and
adult diabetic subjects, its epidemiological and clinical left ventricular hypertrophy (LVH) in DM patients has
correlates. been widely implicated4,5 and therefore considered as a
Methods: A descriptive cross-sectional study involv- treatment target5, as associated cardiovascular risks
ing 534 patients was conducted at the Edward Francis become normal with full regression of LVH.6 Insulin
Small Teaching Hospital (formerly Royal Victoria resistance and associated abnormal glucose metabolism
Teaching Hospital), The Gambia. Four hundred and have been implicated in many reports as a possible
forty patients were included using a standard question- pathophysiological mechanism of LVH. This therefore
naire. Anthropometry, laboratory investigations and highlights the need for the early detection of LVH in
electrocardiogram were carried out. We used the Lew- DM in order to institute a timely effective interven-
is, Cornell, and Sokolow-Lyon Voltage criteria to de- tion.7
fine ECG-LVH. MinitabTM statistical software version
13.20 was used for analysis. Electrocardiogram remains a cheap, useful and a wide-
Results: 146 (35.2%) patients had ECG-LVH using all ly available tool to determine LVH.8 This paper aims to
3 criteria and this prevalence was higher among wom- determine the prevalence of electrocardiographic left
en being 116 (79.5%). A generally high prevalence of ventricular hypertrophy (ECG-LVH) among adult
overweight (155/37.4%) and obesity (119/28.6%) was Gambian DM patients and also to determine its associ-
observed among study participants, and both clinic-day ated clinical factors.
systolic and diastolic blood pressure (BP) were signifi-
cantly higher in those with ECG-LVH. Poor diabetes METHODS
control was observed in both groups. This study was conducted at the Edward Francis Small
Conclusion: There was a high prevalence of ECG- Teaching Hospital (EFSTH) in Banjul, The Gambia
LVH and it is especially so with combining multiple during routine clinic visits (on every Monday and
criteria, hence the need for screening. Clinic-day hy- Wednesday) from the 6th November, 2008 to the 4th
pertension was associated with ECG-LVH hence the January 2009 between the hours of 8am and 2pm.
need for diagnosing and aggressive treatment of hyper-
tension in patients with diabetes mellitus. Study Population: All patients with a confirmed diag-
nosis of DM and who attend the medical out-patient
Keywords: Diabetes mellitus, ECG-LVH, The Gam- department, EFSTH for routine care were eligible for
bia, voltage criteria inclusion into the study. Pregnant women and those
who did not consent for inclusion were excluded.
19
March 2015 M. Jobe et al ECG-LVH in Gambian diabetic patients
Subjects less than 25 years of age and those with bun- Blood and urine samples: Venous blood samples were
dle branch block were excluded from the present anal- collected and analysed using a COBAS INTEGRA
ysis. 400 plus analyser (Roche Diagnostics GmbH) at the
EFSTH laboratories for total cholesterol, high density
Study design: cross-sectional study. lipoprotein cholesterol (HDL-cholesterol), low density
lipoprotein cholesterol (LDL-cholesterol), triglycer-
Questionnaire: a trained research field assistant in a ides, creatinine, fructosamine, albumin and uric acid
language understood by the study participant adminis- levels. Blood glucose was determined using a portable
tered a standard questionnaire designed for the purpose glucometer (Accu-Chek). Urine sample was also col-
of the study. The questionnaire was divided into 3 sec- lected and urine dipstick was done for glucose and pro-
tions. Section A included items on demographic de- tein.
tails like age, sex, address, ethnicity, religion, educa-
tional level, smoking status as well as background de- Electrocardiography: The study participants had a
tails about the participant’s DM. Occupations were standard surface 12-lead ECG recorded with the patient
coded as manual if involving mainly unskilled labour; lying supine and relaxed on a flat surface (using a Car-
as trades for occupations mainly involving skilled dioline Delta 1 EKG Machine). The machine was regu-
manual labour; or as non-manual. The rest were coded larly checked to ensure that it was in a proper working
as others. Section B covered information about the condition. After explaining the procedure to the patient,
usual medical care the patient receives (including activ- the ECG leads were placed according to standard prac-
ities at clinic visits, medications prescribed) and also tice. The paper speed was set at 25mm/s whilst the
evidence of diabetic foot (or feet) complication(s). Sec- voltage set at 10mm/mV. The ECG recordings were
tion C involved carrying out basic anthropometric sent to Aristide Le Dantec Teaching Hospital, in Da-
measurements, blood pressure (BP) measurements, kar, Senegal and analysed by a group of cardiology
urine dipstick, and venous blood sampling for serum residents, supervised by an electrophysiologist with
biochemistry and also obtaining a standard 12-lead many years of experience using a specially designed
surface ECG. protocol. The various parameters studied included the
rhythm, heart rate, PR interval, presence of significant
Blood pressure: Blood pressure and pulse rate were Q wave, LVH (using Lewis, Cornell, and Sokolow-
recorded with an Omron 705IT machine (Omron, Kyo- Lyon voltage criteria) and ST-T changes.
to, Japan) with the participant in a seated position using
the subject’s left arm positioned at heart level. The BP ECG-LVH was defined according to standard criteria
was taken first when the patient enters the consulting using the mean of 3 consecutive QRS values as fol-
room and after five minutes. Two measurements were lows: Lewis voltage as (R wave in lead 1-R wave in
done at each time and the mean of the two readings lead 3)+(S wave in lead 3-S wave in lead 1)≥1.7mV
9
was recorded. Cornell voltage as S wave in V3+ R wave in
aVL≥2.0mV in women and 2.8mV in men10 Sokolow-
Anthropometry: Height was measured without foot- Lyon Voltage as S wave in V1+R wave in V5 or
wear or headwear with the subject standing fully erect V6≥3.5mV 11
on a flat surface, with heels, buttock and shoulders flat
to the height meter, and the subject looking straight Data Management
ahead using a daily calibrated stadiometer (Leicester The data of each participant was collected on a ques-
height measure, Seca 214, Birmingham, UK). Meas- tionnaire which was then entered into Microsoft Excel
urement was done to the nearest 0.5cm. Weight was 2007 by double entry. The data was cross-checked and
measured with the subject wearing light clothing with all inconsistencies were corrected. The data was then
no footwear using a digital scale (Tanita Corporation, transferred to and analyzed using MinitabTM statistical
Tokyo, Japan). The value was recorded to the nearest software version 13.20. The characteristics of patients
0.1kg. Waist circumference measured at the level of with ECG-LVH and those without it were compared
the upper margin of the iliac crest, was measured to the using two-sample t-test for continuous variables and
nearest centimeter with a flexible tape. Body mass in- Chi-square test for categorical variables. P-values of
dex (BMI) was defined as weight (kg)/height (m).2 We less than 0.05 were considered to be of statistical sig-
used a new generation foot-to-foot bioimpedence de- nificance.
vice (Tanita TBF300GS, Tanita Corporation) to meas-
ure fat percent, fat mass, total body water (TBW) with Ethical Consideration
the subject standing erect in bare feet on the bioim- The School of Medicine and Allied Health Sciences,
pedence analyzer. University of the Gambia Research and Publication
Committee approved the study protocol.
20
March 2015 Volume 49, Number 1 GHANA MEDICAL JOURNAL
An informed consent was obtained from each of the As shown in Table 2, there was no significant differ-
study participants after explanation and careful consid- ence in the age of patients with or without ECG-LVH
eration by the participant signing or thumbs printing a both at the time of diagnosis of diabetes and also at the
written consent form. time of the study.
21
March 2015 M. Jobe et al ECG-LVH in Gambian diabetic patients
It has been demonstrated from previous studies that Women with DM have been shown to have a higher
ECG has a lower sensitivity compared to echocardiog- cardiovascular morbidity and mortality than their male
raphy in determining LVH.12 Generally, black individ- counterparts.23, 24, 25 Therefore the higher prevalence of
uals have greater precordial QRS voltages than whites females with LVH and obesity in this cohort is worry-
and many of the LVH criteria have higher sensitivity in ing and needs attention.
detecting LVH in blacks and lower specificity com-
pared with whites.13,14 However, many of the criteria We advocate for the early detection and aggressive
proposed like the Araoye for African blacks are yet to treatment of LVH to prevent potentially life-
be validated and so far have offered no comparative threatening consequences. Many antihypertensive
advantage over the standard criteria.15 agents have been recommended for the treatment of
LVH. However, agents with intrinsic sympathomimetic
Additionally many factors might limit the accuracy of properties or with direct vasodilatory effects (e.g. hy-
ECG in determining LVH including age, body habitus, dralazine and minoxidil) must be avoided.26 The most
obesity and chronic lung diseases. Hence many au- effective agents in reducing left ventricular mass are
thors advocate the use of echocardiography to deter- angiotensin II receptor blockers, angiotensin-
mine LVH. However, the availability of echocardiog- converting enzyme inhibitor, calcium channel blockers
raphy is still limited and not feasible in many places and diuretics.27 Bauml and Underwood recommend
especially in our sub-region. Besides the unavailability that treatment should consist of an angiotensin II recep-
of technical expertise to operate echocardiography in tor blocker or an angiotensin-converting enzyme inhib-
many places, high costs further limits its usage. The itor 28 which have additional renoprotective effect as
present study compared different voltage criteria and well as reversing LVH. However, these agents are less
showed the superiority of using more than one criterion efficacious in blacks according to the investigators of
to determine ECG-LVH. This is advocated by many Studies of Left Ventricular Dysfunction (SOLVED) 29
authors and has been demonstrated in various stud- but who have been shown to benefit from treatment
ies.16,17,18 with diuretic agents.26
22
March 2015 Volume 49, Number 1 GHANA MEDICAL JOURNAL
mass in the Framingham Heart Study. N Eng J 15. Dada A, Adebiyi AA, Aje A, Falase AO. Compar-
Med. 1990; 322: 1561-1566 ison of Araoye's criteria with standard electrocar-
4. Srivastava PM, Calafiora P, MacIsaac RJ, Patel diographic criteria for diagnosis of left ventricular
SK, Thomas MC, Jerums G, Burrell LM. Preva- hypertrophy in Nigerian hypertensives. West Afr J
lence and predictors of cardiac hypertrophy and Med. 2006; 25(3):179-85.
dysfunction in patients with type 2 diabetes. Clin 16. Hameed W, Razi MS, Khan MA, Hussain MM,
Sci (Lond). 2008; 114:313-320 Aziz S, Habib SS, Aslam M. Electrocardiographic
5. Dawson A, Morris AD, Struthers A D. The epide- diagnosis of left ventricular hypertrophy: compari-
miology of left ventricular hypertrophy in type 2 son with echocardiography. Pak J Physiol. 2005;
diabetes mellitus. Diabetologia. 2005; 48:1971- 1(1):35-38
1979 17. Erice B, Romero C, Andériz M, Gorostiaga E,
6. Bruno G, Giunti S, Bargero G, Ferrero S, Pagano Izquierdo M, Ibáñez J. Diagnostic value of differ-
G, Perin PC. Sex-differences in prevalence of elec- ent electrocardiographic voltage criteria for hyper-
trocardiographic left ventricular hypertrophy in trophic cardiomyopathy in young people. Scand J
Type 2 diabetes: The Casale Monferrato Study. Med Sci Sports. 2009; 19: 356–363.
Diabet Med. 2004; 21: 823–828 18. Song A, Li TC, Wang NL, Liang YB, Peng Y.
7. Dawson A, Struthers A D. Screening for treatable Better criterion screening for left ventricular hy-
left ventricular abnormalities in diabetic patients. pertrophy by electrocardiogram with different pur-
Expert Opin Biol Ther. 2003; 3(1):107-112 poses. African Journal of Microbiology Research.
8. Nkum BC, Nyan O, Corrah T, Ankrah TC, Allen 2011; 5(14) :1740-1746
S, Micah FB, McAdam K. Resting electrocardio- 19. Desai CS, Ning H, Lloyd-Jones DM. Competing
graphic and echocardiographic findings in an ur- cardiovascular outcomes associated with electro-
ban community in The Gambia. Journal of Science cardiographic left ventricular hypertrophy: the
and Technology (Ghana). 2009; 29(1):130-140 Atherosclerosis Risk in Communities Study.
9. Lewis T. Observations upon ventricular hypertro- Heart. 2012; 98:330-334.
phy with special reference to preponderance of one 20. Niiranen TJ, Jula AM, Kantola IM, Karanko
or another chamber. Heart. 1914; 5: 367-403. H, Reunanen A. Home-measured blood pressure is
10. Cascale PN, Devereux RB, Alonso DR, Campo more strongly associated with electrocardiographic
E, Kligfield P. Improved sex-specific criteria of left ventricular hypertrophy than is clinic blood
left ventricular hypertrophy for clinical and com- pressure: the Finn-HOME study. J Hum Hyper-
puter interpretation of electrocardiograms: valida- tens. 2007 ; 21 (10):788–794.
tion with autopsy findings. Circulation. 1987; 21. Kuller LH, Eichner JE, Orchard TJ, Grandits
75(3):565-72. GA, McCallum L, Tracy RP. The relation be-
11. Sokolow M, Lyon TP. The ventricular complex in tween serum albumin levels and risk of coronary
left ventricular hypertrophy as obtained by unipo- heart disease in the Multiple Risk Factor Interven-
lar precordial and limb leads. Am Heart J. 1949; tion Trial. Am J Epidemiol. 1991; 134(11):1266-77
37: 161-86. 22. van der Sande MAB, Ceesay SM, Miligan PJM,
12. Somaratne JB, Whalley GA, Poppe KK, ter Bals Banya WAS, Prentice A, McAdam KPWJ,
MM, Wadams G, Pearl A, Bagg W, Doughty RN. Walraven GEL. Obesity and Undernutrition and
Screening for left ventricular hypertrophy in pa- Cardiovascular Risk Factors in Rural and Urban
tients with type 2 diabetes mellitus in the commu- Gambian Communities. Am J Public Health. 2001;
nity. Cardiovasc Diabetol. 2011; 10:29. 91(10):1641-1644
13. Chapman JN, Mayet J, Chang CL, Foale 23. Tenenbaum A, Fisman EZ, Schwammenthal E,
RA, Thom SA, Poulter NR. Ethnic differences in Adler Y, Benderly M, Motro M, Shemesh J. In-
the identification of left ventricular hypertrophy in creased prevalence of left ventricular hypertrophy
the hypertensive patient. Am J Hyper- in hypertensive women with type 2 diabetes melli-
tens. 1999;12(5):437-42 tus. Cardiovasc Diabetol. 2003; 2:14
14. Okin PM, Wright JT, Nieminen MS, Jern 24. Marks JB, Raskin P. Cardiovascular risk in diabe-
S, Taylor AL, Phillips R, Papademetriou V, Clark tes: a brief review. J Diabetes Complications.
LT, Ofili EO, Randall OS, Oikarinen L, Viitasalo 2000; 14:108-115
M, Toivonen L, Julius S, Dahlöf B, Devereux RB. 25. Galcera-Tomas J, Melgarejo-Moreno A, Garcia-
Ethnic differences in electrocardiographic criteria Alberola A, Rodriguez-Garcia P, Lozano-Martinez
for left ventricular hypertrophy: the LIFE study. J, Martinez-Hernandez J, Martinez-Fernandez S.
Losartan Intervention For Endpoint. Am J Hyper- Prognostic significance of diabetes in acute myo-
tens. 2002; 15 (8):663-71. cardial infarction. Are the differences linked to
female gender? Int J Cardiol. 1999; 69:289-298.
23
March 2015 M. Jobe et al ECG-LVH in Gambian diabetic patients
26. Liebson PR . Left ventricular hypertrophy. Curr 29. Exner DV, Dries DL, Domanski MJ, Cohn J.
Treat Options Cardiovasc Med. 1999;1:219–230 Lesser response to angiotensin-converting-enzyme
27. Lip GYH. Regression of Left Ventricular Hyper- inhibitor therapy in black as compared with white
trophy and Improved Prognosis. Circulation. patients with left ventricular dysfunction. N Engl J
2001; 104:1582-1584 Med. 2001; 344:1351–1357-31 ✪
28. Bauml MA, Underwood DA. Left ventricular hy-
pertrophy: An overlooked cardiovascular risk fac-
tor. Cleve Clin J Med. 2010; 77: 381-387
24