MICROALBUMINURIA: ASSOCIATION WITH ISCHAEMIC HEART DISEASE IN NON-DIABETICS
Abstract
Background: In view of the high morbidity and mortality associated with ischemic heart disease(IHD), the estimation of individual cardiovascular risk over and above the assessment of classic
risk factors, such as age, hypercholesterolemia and hypertension, is an important prerequisite for
focusing preventive measures and therapeutic measures. Microalbuminuria (MA) as a marker of
IHD in nondiabetics is currently under international debate. The present descriptive study
undertaken at Combined Military Hospital, Lahore was aimed to determine the frequency of MA
in nondiabetic IHD patients. Methods: One hundred consecutive non diabetic patients with IHD
(73 males, 27 females). Patients showing clinical albumiuria and with other causes of proteinuria
were excluded. Urinary albumin in first morning sample was estimated by immunoturbidimetry
method. Albumin to creatinine ratio (ACR) was calculated as mg/g. Results: The frequency of
MA ( ACR > 30 mg/g) was 37% in patients. Frequency was highest in older age bracket for both
genders. The mean ACR was 131.8±66.2 mg/g. Significant difference was observed in mean MA
level among different age groups. Conclusion: MA is common in nondiabetics patients with IHD.
The mean level of MA was higher in older patients.
Key Words: Ischemic heart disease, nondiabetics, microalbuminuria, cardiovascular risk.
References
Murray CJL, Lopez AD. The global burden of disease: a
comprehensive assessment of mortality and disability from
diseases, injuries, and risk factors in 1990 and projected to
Cambridge, Mass: Harvard University Press; 1996.
McGovern PG, Pankow JS, Shahar E, Doliszny KM, Folsom
AR, Blackburn H, et al. The Minnesota Heart Survey
Investigators. Recent trends in acute coronary heart disease:
mortality, morbidity, medical care, and risk factors. N Engl J
Med 1996; 334:884-90.
Yusuf S, Reddy S, Ôunpuu S, Anand S. Global burden of
cardiovascular diseases. Part II: Variations in cardiovascular
disease by specific ethnic groups and geographic regions and
prevention strategies. Circulation 2001; 104:2855 - 64.
Abbas S, Abbas S, Riaz A, Malik N. Risk factors for
coronary artery disease in Pakistan. Pak Armed Forces Med J
; 53(1):12-19.
Khan JA, Khan SP, Ahmed Z, Shah SH, Khaliq MA. Level
of hypercholesterolemia in patients admitted for heart
diseases: a pilot study. Pak J Med Res 2001; 40:18-9.
Nyuyen TT, Elleform RD, Hodge DO, Balles KR, Kolthe
TE, Abu-Leddhl. Lp (a) as a risk factor for cardiovascular
disease. Circulation 1997; 96: 1390-7.
J Ayub Med Coll Abbottabad 2006;18(1)
Ridker PM, Cushman M, Stampfer MJ, Tracy RP,
Hennekens CH. Inflammation, aspirin, and the risk of
cardiovascular disease in apparently healthy men. N Engl J
Med 1997; 336: 973-9.
Ridker PM, Hennekens CH, Buring JE, Rifai N. C-reactive
protein and other markers of inflammation in the prediction
of cardiovascular disease in women. N Engl J Med 2000;
: 836-43.
MA J, Hennekens CH, Ridker PM, Stampfer MJ. A
prospective study of fibrinogen and risk of myocardial
infarction in the Physicians' Health Study. J Am Coll Cardiol
; 33:1347-52.
Christen WG, Ajani UA, Glynn RJ, Hennekens CH. Blood
levels of homocysteine and increased risks of cardiovascular
disease: causal or casual? Arch Intern Med 2000; 160: 422-
Viberti GC, Thomas SM. Searching for new coronary heart
disease risk factors. Eur Heart J 2000; 21:1905-6.
Ali I, Khan I, Baloch MK, Mustafa G. Comparative lipd
profile studies in cardiac and diabetic patients. Pak J
Pharmaceut Sci 2004; 17:25-30.
Parving HH, Osterby R, Ritz E. Diabetic nephropathy. In:
Brenner BM, Levine S (edi). The Kidney. Philadelphia: WB
Saunders; 2000:1731-73.
Garg JP, Bakris GL. Microalbuminuria: marker of
cardiovascular dysfunction, risk factor for cardiovascular
disease. Vasc Med 2002; 7:35-43.
Hillege HL, Janssen WMT, Bak AAA, Diercks GFH,
Grobbee DE, Crijns HJGM et al. Microalbumniuria is
common, also in a nondiabetic, nonhypertensive population,
and an independent indicator of cardiovascular risk factors
and cardiovascular morbidity. J Inter Med 2001; 249:519-26.
Jensen JS. Microalbuminaria and the risk of atherosclerosis.
Clinical, epidemiological and physiological investigations.
Dan Med Bull 2000; 47(2):63-78.
Lloyd DR, Hindle EJ, Marples J, Gatt JA. Urinary albumin
measurements by immunoturbidimetry. Ann Clin Biochem
; 24:(Pt2) 209-10.
Yudkin JS, Forrest RD, Jackson CA. Microalbuminuria as
predictor of vascular disease in non-diabetic subjects.
Islington Diabetes Survey. Lancet 1988; ii: 530-3.
Ritz E, Nowicki M, Fliser D, Horner D, Klin HP. Proteinuria
and hypertension. Kidney Int 1994; 46 (Suppl 47):S76-80.
Cirillo M, Senigalliesi L, Laurenzi M, Alfieri R, Stamler J,
Stamler R et al. Microalbuminuria in non-diabetic adults:
relation of blood pressure, body mass index, plasma
cholesterol levels, and smoking: The Gubbio Population
Study. Arch Intern Med 1998; 158: 1933-9.
Taskiran M, Feldt-Rasmussen B, Jensen GB, Jensen JS.
Urinary albumin Excretion in hospitalized patients with acute
myocardial infarction. Scand Cardiovasc J 1998; 32:163-6.
Venkatt KK. Proteinuria and microalbuminuria in adults:
significance, evaluation and treatment. South Med J 2004;
(10):969-79.
Borch-Johnsen K, Feldt-Rasmussen B, Strandgaard S,
Schroll M, Jensen JS. Urinary albumin excretion. An
independent predictor of ischemic heart disease. Arterioscler
Thromb Vasc Biol 1999; 19:1992-7.
Damsgaard EM, Froland A, Jorgensen OD, Mogensen CE.
Microalbuminuria as predictor of increased mortality in
elderly people. BMJ 1990; 300: 297-300.
Jensen JS. Renal and systemic transvascular albumin leakage
in severe atherosclerosis. Arterioscler Thromb Vasc Biol
; 15: 1324-29.
Berton G, Cordiano R, Palmieri R, Cicchini F, DeToni R,
Palitini P. Microalbuminuria during acute myocardial
infarction. Eur Heart J 2001; 22:1466-1475
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