Beneficial effects of intensive therapy of diabetes during adolescence: Outcomes after the conclusion of the Diabetes Control and Complications Trial (DCCT)

被引:334
作者
Genuth, S [1 ]
Nathan, D
Shamoon, H
Duffy, H
Engel, S
Engel, H
Dahms, W
Mayer, L
Pendegras, S
Zegarra, H
Miller, D
Singerman, L
Brillion, D
Lackaye, M
Heinemann, M
Rahhal, F
Reppuci, V
Lee, T
Whitehouse, F
Kruger, D
Carey, JD
Bergenstal, R
Johnson, M
Kendall, D
Spencer, M
Noller, D
Morgan, K
Etzwiler, D
Jacobson, A
Golden, E
Soroko, D
Sharuk, G
Arrigg, P
Doyle, J
Nathan, D
Fritz, S
Crowell, S
Godine, J
McKitrick, C
Lou, P
Service, J
Ziegler, G
Pach, J
Colwell, J
Wood, D
Mayfield, R
Hermayer, K
Szpiech, M
Lyons, T
Parker, J
机构
[1] Albert Einstein Coll Med, Bronx, NY USA
[2] Case Western Reserve Univ, Clin Coordinating Ctr, Cleveland, OH 44106 USA
[3] Cornell Univ, Med Ctr, Ithaca, NY 14853 USA
[4] Joslin Diabet Ctr, Boston, MA 02215 USA
[5] Massachusetts Gen Hosp, Boston, MA 02114 USA
[6] Mayo Clin & Mayo Fdn, Rochester, MN 55905 USA
[7] Med Univ S Carolina, Charleston, SC 29425 USA
[8] Northwestern Univ, Evanston, IL 60208 USA
[9] Univ Calif San Diego, La Jolla, CA 92093 USA
[10] Univ Iowa, Iowa City, IA 52242 USA
[11] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[12] Univ Michigan, Ann Arbor, MI 48109 USA
[13] Univ Minnesota, Minneapolis, MN 55455 USA
[14] Univ Missouri, Columbia, MO 65211 USA
[15] Univ New Mexico, Albuquerque, NM 87131 USA
[16] Univ Penn, Philadelphia, PA 19104 USA
[17] Univ Pittsburgh, Pittsburgh, PA 15260 USA
[18] Univ S Florida, Tampa, FL 33620 USA
[19] Univ Tennessee, Knoxville, TN 37996 USA
[20] Univ Texas, SW Med Ctr, Dallas, TX 75235 USA
[21] Univ Toronto, Toronto, ON, Canada
[22] Univ Washington, Lipoprot Distribut Grp, Seattle, WA 98195 USA
[23] Univ Western Ontario, London, ON N6A 3K7, Canada
[24] Vanderbilt Univ, Nashville, TN 37240 USA
[25] Washington Univ, St Louis, MO 63130 USA
[26] Yale Univ, Sch Med, New Haven, CT 06520 USA
[27] George Washington Univ, Data Coordinating Ctr, Ctr Biostat, Washington, DC 20052 USA
[28] NIDDKD, Program Off, Bethesda, MD USA
[29] Univ Wisconsin, Cent Fundus Photograph Reading Ctr, Madison, WI 53706 USA
[30] Univ Minnesota, Cent Biochem Lab, Minneapolis, MN 55455 USA
[31] Univ Minnesota, Cent ECG Reading Unit, Minneapolis, MN 55455 USA
[32] Med Univ S Carolina, Mol Risk Factors Program Project, Charleston, SC USA
[33] Hosp Sick Children, Genet Studies Grp, Toronto, ON, Canada
关键词
D O I
10.1067/mpd.2001.118887
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
Objective: The Diabetes Control and Complications Trial (DCCT) demonstrated that intensive therapy of type I diabetes mellitus reduces the risk of development and progression of microvascular complications. The Epidemiology, of Diabetes Interventions and Complications (EDIC) study assessed whether these benefits persisted after the end of DCCT. Results for the adolescent DCCT cohort are reported here. Study design: Of the DCCT adolescent cohort (n = 195), 175 participated in EDIC, 151 had fundus photography, and 156 had albumin excretion rate measured at year 3 or 4. The odds of progression of retinopathy and albuminuria from closeout of the DCCT until ED IC year 4 were assessed. Results: In contrast to the 7.4 years of the DCCT during which mean hemoglobin A,, levels were significantly lower with intensive therapy than conventional therapy (8.06% vs 9.76%; P < .0001), the subsequent first 4 years of EDIC had mean hemoglobin Alc levels that were similar between the former intensive and the former conventional groups (8.38% vs 8.45%). However, the prevalence of worsening of 3 steps or more in retinopathy and of progression to proliferative or severe nonproliferative retinopathy were reduced by 74% (P < .001) and 78% (P < .007), respectively, in the former intensive therapy group compared with the Former conventional group. Conclusions: These findings provide further support for the DCCT recommendation that most adolescents with type I diabetes receive intensive therapy aimed at achieving glycemic control as close to normal as possible to reduce the risk of microvascular complications.
引用
收藏
页码:804 / 812
页数:9
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