THE EFFECT OF INTENSIVE TREATMENT OF DIABETES ON THE DEVELOPMENT AND PROGRESSION OF LONG-TERM COMPLICATIONS IN INSULIN-DEPENDENT DIABETES-MELLITUS

被引:9813
|
作者
SHAMOON, H
DUFFY, H
FLEISCHER, N
ENGEL, S
SAENGER, P
STRELZYN, M
LITWAK, M
WYLIEROSETT, J
FARKASH, A
GEIGER, D
ENGEL, H
FLEISCHMAN, J
POMPI, D
GINSBERG, N
GLOVER, M
BRISMAN, M
WALKER, E
THOMASHUNIS, A
GONZALEZ, J
GENUTH, S
BROWN, E
DAHMS, W
PUGSLEY, P
MAYER, L
KERR, D
LANDAU, B
SINGERMAN, L
RICE, T
NOVAK, M
SMITHBREWER, S
MCCONNELL, J
DROTAR, D
WOODS, D
KATIRGI, B
LITVENE, M
BROWN, C
LUSK, M
CAMPBELL, R
LACKAYE, M
RICHARDSON, M
LEVY, B
CHANG, S
HEINHEINEMANN, M
BARRON, S
ASTOR, L
LEBECK, D
BRILLON, D
DIAMOND, B
VASILASDWOSKIN, A
LAURENZI, B
机构
[1] YESHIVA UNIV ALBERT EINSTEIN COLL MED, BRONX, NY 10461 USA
[2] CASE WESTERN RESERVE UNIV, CLEVELAND, OH 44106 USA
[3] CORNELL UNIV, MED CTR, NEW YORK, NY 10021 USA
[4] HENRY FORD HOSP, DETROIT, MI 48202 USA
[5] INT DIABET CTR, MINNEAPOLIS, MN USA
[6] JOSLIN DIABET CTR, BOSTON, MA USA
[7] MASSACHUSETTS GEN HOSP, BOSTON, MA 02114 USA
[8] MAYO CLIN & MAYO FDN, ROCHESTER, MN 55905 USA
[9] MED UNIV S CAROLINA, CHARLESTON, SC 29425 USA
[10] NORTHWESTERN UNIV, EVANSTON, IL 60201 USA
[11] UNIV BRITISH COLUMBIA, VANCOUVER V6T 1W5, BC, CANADA
[12] UNIV CALIF SAN DIEGO, LA JOLLA, CA 92093 USA
[13] UNIV IOWA, IOWA CITY, IA 52242 USA
[14] UNIV MARYLAND, SCH MED, BALTIMORE, MD 21201 USA
[15] UNIV MICHIGAN, ANN ARBOR, MI 48109 USA
[16] UNIV MINNESOTA, CENT BIOCHEM LAB, MINNEAPOLIS, MN 55455 USA
[17] UNIV MISSOURI, CENT BACKUP LAB HBAIC, COLUMBIA, MO 65201 USA
[18] UNIV NEW MEXICO, SCH MED, ALBUQUERQUE, NM 87131 USA
[19] UNIV PENN, CHILDRENS HOSP, PHILADELPHIA, PA 19104 USA
[20] UNIV PITTSBURGH, PITTSBURGH, PA 15260 USA
[21] UNIV S FLORIDA, TAMPA, FL 33620 USA
[22] UNIV TENNESSEE, KNOXVILLE, TN 37996 USA
[23] UNIV TEXAS, SW MED CTR, DALLAS, TX 75230 USA
[24] UNIV TORONTO, TORONTO M5S 1A1, ONTARIO, CANADA
[25] UNIV WASHINGTON HOSP, SEATTLE, WA 98105 USA
[26] UNIV WESTERN ONTARIO, LONDON N6A 3K7, ONTARIO, CANADA
[27] VANDERBILT UNIV, NASHVILLE, TN 37240 USA
[28] WASHINGTON UNIV, ST LOUIS, MO 63130 USA
[29] YALE UNIV, SCH MED, NEW HAVEN, CT 06510 USA
[30] NIDDKD, PROGRAM OFF, BETHESDA, MD USA
[31] SO ILLINOIS UNIV, CENT AUTONOM CODING UNIT, CARBONDALE, IL 62901 USA
[32] UNIV WISCONSIN, CENT FUNDUS PHOTOG READING CTR, MADISON, WI 53706 USA
[33] WESTERN PSYCHIAT INST & CLIN, CENT NEUROBEHAV CODING UNIT, PITTSBURGH, PA 15261 USA
[34] UNIV MINNESOTA, CENT ECG READING UNIT, MINNEAPOLIS, MN 55455 USA
[35] UNIV MINNESOTA, CENT NUTR CODING UNIT, MINNEAPOLIS, MN 55455 USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 1993年 / 329卷 / 14期
关键词
D O I
10.1056/nejm199309303291401
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Long-term microvascular and neurologic complications cause major morbidity and mortality in patients with insulin-dependent diabetes mellitus (IDDM). We examined whether intensive treatment with the goal of maintaining blood glucose concentrations close to the normal range could decrease the frequency and severity of these complications. Methods. A total of 1441 patients with IDDM - 726 with no retinopathy at base line (the primary-prevention cohort) and 715 with mild retinopathy (the secondary-intervention cohort) were randomly assigned to intensive therapy administered either with an external insulin pump or by three or more daily insulin injections and guided by frequent blood glucose monitoring or to conventional therapy with one or two daily insulin injections. The patients were followed for a mean of 6.5 years, and the appearance and progression of retinopathy and other complications were assessed regularly. Results. In the primary-prevention cohort, intensive therapy reduced the adjusted mean risk for the development of retinopathy by 76 percent (95 percent confidence interval, 62 to 85 percent), as compared with conventional therapy. In the secondary-intervention cohort, intensive therapy slowed the progression of retinopathy by 54 percent (95 percent confidence interval, 39 to 66 percent) and reduced the development of proliferative or severe nonproliferative retinopathy by 47 percent (95 percent confidence interval, 14 to 67 percent). In the two cohorts combined, intensive therapy reduced the occurrence of microalbuminuria (urinary albumin excretion of greater-than-or-equal-to 40 mg per 24 hours) by 39 percent (95 percent confidence interval, 21 to 52 percent), that of albuminuria (urinary albumin excretion of greater-than-or-equal-to 300 mg per 24 hours) by 54 percent (95 percent confidence interval, 19 to 74 percent), and that of clinical neuropathy by 60 percent (95 percent confidence interval, 38 to 74 percent). The chief adverse event associated with intensive therapy was a two-to-threefold increase in severe hypoglycemia. Conclusions. Intensive therapy effectively delays the onset and slows the progression of diabetic retinopathy, nephropathy, and neuropathy in patients with IDDM.
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收藏
页码:977 / 986
页数:10
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