TY - JOUR
T1 - The development and progression of diabetic retinopathy in type I diabetic patients
T2 - A cohort study
AU - Kalter-Leibovici, O.
AU - Leibovici, L.
AU - Loya, N.
AU - Kremer, I.
AU - Axer-Siegel, R.
AU - Karp, M.
AU - Laron, Z.
PY - 1997
Y1 - 1997
N2 - To describe the course and risk factors for development and progression of retinopathy, we studied a cohort of 333 Israeli Jewish patients with Type 1 (insulin-dependent) diabetes mellitus. The median age at diagnosis was 9.5 (range 0.04-26.2) years and the median duration of follow-up was 14 (range 1.6-30) years. Evaluation of both retinae was performed yearly since referral and HbA1 values were tested every 3 months since 1978. During a follow-up of 4070 patient-years, 162 patients developed non-proliferative retinopathy. The median retinopathy-free interval was 14.9 years and after 30 years all patients were affected. Pre-pubertal duration of diabetes was relevant. Independent and significant risk factors for early onset of non-proliferative retinopathy were: poor cumulative glycaemic control (median retinopathy-free interval in the 1st vs 4th quartiles of mean HbA1 values over all years: 18.0 vs 12.5 years, p = 0.0001); onset of diabetes during or after puberty (median retinopathy-free interval in patients with onset of diabetes before, during or after pubescence: 16.3, 13.2 and 14.0 years, respectively, p= 0.0001); and non-Ashkenazi Jewish origin (median retinopathy-free interval 15.8 years in Asbkenazi vs 14.0 in non-Ashkenazi patients, p = 0.0004). Of 162 patients with non-proliferative retinopathy, progression to proliferative retinopathy occurred in 37, during 707 patient-years. The first event of proliferative retinopathy was diagnosed within the 1st year after non- proliferative retinopathy evolved, and at 6.3 years since onset of non- proliferative retinopathy 75% of the patients were still free of proliferative changes. Risk factors significantly and independently associated with an early progression to the proliferative stage were: poor glycaemic control in the last 3 years prior to the development of proliferative retinopathy and non-Ashkenazi Jewish origin. All patients in the 4th quartile of HbA1 values were affected by proliferative retinopathy within 11.6 years after onset of non-proliferative retinopathy.
AB - To describe the course and risk factors for development and progression of retinopathy, we studied a cohort of 333 Israeli Jewish patients with Type 1 (insulin-dependent) diabetes mellitus. The median age at diagnosis was 9.5 (range 0.04-26.2) years and the median duration of follow-up was 14 (range 1.6-30) years. Evaluation of both retinae was performed yearly since referral and HbA1 values were tested every 3 months since 1978. During a follow-up of 4070 patient-years, 162 patients developed non-proliferative retinopathy. The median retinopathy-free interval was 14.9 years and after 30 years all patients were affected. Pre-pubertal duration of diabetes was relevant. Independent and significant risk factors for early onset of non-proliferative retinopathy were: poor cumulative glycaemic control (median retinopathy-free interval in the 1st vs 4th quartiles of mean HbA1 values over all years: 18.0 vs 12.5 years, p = 0.0001); onset of diabetes during or after puberty (median retinopathy-free interval in patients with onset of diabetes before, during or after pubescence: 16.3, 13.2 and 14.0 years, respectively, p= 0.0001); and non-Ashkenazi Jewish origin (median retinopathy-free interval 15.8 years in Asbkenazi vs 14.0 in non-Ashkenazi patients, p = 0.0004). Of 162 patients with non-proliferative retinopathy, progression to proliferative retinopathy occurred in 37, during 707 patient-years. The first event of proliferative retinopathy was diagnosed within the 1st year after non- proliferative retinopathy evolved, and at 6.3 years since onset of non- proliferative retinopathy 75% of the patients were still free of proliferative changes. Risk factors significantly and independently associated with an early progression to the proliferative stage were: poor glycaemic control in the last 3 years prior to the development of proliferative retinopathy and non-Ashkenazi Jewish origin. All patients in the 4th quartile of HbA1 values were affected by proliferative retinopathy within 11.6 years after onset of non-proliferative retinopathy.
KW - Cohort study
KW - Diabetic retinopathy
KW - Ethnic origin
KW - Glycaemic control
KW - Puberty
KW - Type 1 diabetes
UR - http://www.scopus.com/inward/record.url?scp=0030768448&partnerID=8YFLogxK
U2 - 10.1002/(SICI)1096-9136(199710)14:10<858::AID-DIA471>3.0.CO;2-V
DO - 10.1002/(SICI)1096-9136(199710)14:10<858::AID-DIA471>3.0.CO;2-V
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AN - SCOPUS:0030768448
SN - 0742-3071
VL - 14
SP - 858
EP - 866
JO - Diabetic Medicine
JF - Diabetic Medicine
IS - 10
ER -