Microalbuminuria and urinary albumin excretion: French clinical practice guidelines

被引:21
作者
Halimi, J.-M. [1 ]
Hadjadj, S.
Aboyans, V.
Allaert, F.-A.
Artigou, J.-Y.
Beaufils, M.
Berrut, G.
Fauvel, J.-P.
Gin, H.
Nitenberg, A.
Renversez, J.-C.
Rusch, E.
Valensi, P.
Cordonnier, D.
机构
[1] CHU Tours, Serv Nephrol Immunol Clin, F-37044 Tours, France
[2] CHU Poitiers, INSERM, ERM 324, Serv Endocrinol, F-86021 Poitiers, France
[3] CHU Limoges, Hop Dupuytren, Serv Chirurg Thorac & Cardiovasc & Angiol, Limoges, France
[4] CHRU Dijon, DIM, Dijon, France
[5] Hop Avicenne, Hop Avicenne, Serv Cardiol, F-93009 Bobigny, France
[6] Hop Tenon, Serv Med Interne, F-75020 Paris, France
[7] CHU Angers, Serv Gerontol Clin, F-49933 Angers, France
[8] Hop Edouard Herriot, Dept Hypertens & Nephrol, Lyon, France
[9] Univ Bordeaux 1, Serv Diabetol, F-33604 Pessac, France
[10] Univ Paris 08, CHU Jean Verdier, Serv Explorat Fonctionelles, F-93140 Bondy, France
[11] CHU Grenoble, Hop A Michallon, Dept Biol Integree, F-38043 Grenoble, France
[12] CHU Tours, Serv Informat Med, F-37044 Tours, France
[13] Univ Paris 13, Hop Jean Verdier, APHP, Serv Endocrinol Diabetol Nutr, Bondy, France
[14] CHU Grenoble, Serv Nephrol, F-38043 Grenoble, France
[15] Univ Montreal, Dept Epidemiol McGill, Montreal, PQ, Canada
关键词
albuminuria; cardiovascular risk; diabetes mellitus; renal failure; hypertension;
D O I
10.1016/j.diabet.2007.06.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Urinary albumin excretion (UAE) may be assayed on a morning urinary sample or a 24 h-urine sample. Values defining microalbuminuria are: 1) 24-h urine sample: 30-300 mg/24 h; 2) morning urine sample: 20-200 mg/ml or 30-300 mg/g creatinine or 2.5-25 mg/mmol creatinine (men) or 3.5-35 mg/mmol (women); 3) timed urine sample: 20-200 mu g/min. The optimal use of semi-quantitative urine test-strip is not clearly defined. It is generally believed that microalbuminuria reflects a generalized impairment of the endothelium; however, no definite proof has been obtained in humans. In diabetic subjects. - Microalbuminuria is a marker of increased risk of cardiovascular (CV) and renal morbidity and mortality in type I and type 2 diabetic subjects. The increase in UAE during follow-up is associated with greater CV and renal risks in type I and type 2 diabetic subjects; its decrease during follow-up is associated with lower risks. In non-diabetic subjects. - Microalbuminuria is a marker of increased risk for diabetes mellitus, deterioration of renal function, CV morbidity and all-cause mortality. It is a marker of increased risk for the development of hypertension in normotensive subjects, and is associated with unfavorable outcome in patients with cancer and lymphoma. Persistence of elevated UAE during follow-up is associated with poor outcome in some hypertensive subjects. Measurement of UAE may be recommended in hypertensive medium-risk subjects with I or 2 CV risk factors in whom CV risk remains difficult to assess, and in those with refractory hypertension: microalbuminuria indicates a high CV risk and must lead to strict control of arterial pressure. Studies focused on microalbuminuria in non-diabetic non-hypertensive subjects are limited; most of them suggest that microalbuminuria predicts CV complications and deleterious outcome. Subjects with a history of CV or cerebrovascular disease have an even greater CV risk if microalbuminuria is present than if it is not; however, in all cases, therapeutic intervention must be aggressive regardless of whether microalbuminuria is present or not. It is not recommended to measure UAE in non-diabetic non-hypertensive subjects in the absence of history of renal disease. Monitoring of renal function (UAE, serum creatinine and estimation of GFR) is recommended annually in all subjects with microalbuminuria. Management. - In patients with microalbuminuria, weight reduction, sodium restriction (< 6 g per day), smoking cessation, strict glucose control in diabetic subjects, strict arterial pressure control are necessary; in diabetic subjects: use of maximal doses of angiotensin-converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB) are recommended; ACEI/ARB and thiazides have synergistic actions on arterial pressure and reduction of UAE; in non-diabetic subjects, any of the five classes of anti-hypertensive medications (ACEI, ARB, thiazides, calcium channel blockers or beta-blockers) can be used. (C) 2007 Elsevier Masson SAS. All rights reserved.
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页码:303 / 309
页数:7
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