Diabetes is an important problem encountered in thalassemic patients. The severity and type of glucose disturbances vary greatly in different studies. Also the pathogenesis seems to be complex; either insulin deficiency or insulin resistance may mediate the glucose disturbances. In a group of thalassemic patients glucose homeostasis was evaluated. Diabetes prevalence was 1.8%. Forty patients were investigated both with an oral glucose tolerance test and first-phase insulin response. Three patients had impaired fasting glucose, 1 patient had impaired glucose tolerance, and 2 patients had hyperinsulinism. Nineteen of 40 patients who were tested had low first-phase insulin response (47.5%) with below 10th centile. Age, BMI, height SDS, age at diagnosis, age at first blood transfusion, number of blood transfusions in a year, percentage of elevated liver enzyme, and hemoglobin and ferritin levels were not different between patients with low first-phase insulin response to patients with normal first-phase insulin response. Four patients are HCV infected, and only 1 of them had low first-phase insulin response. The study group showed a high rate of impairement in insulin secretion by first-phase insulin response to glucose overload, despite the low rate of insulin resistance. Defect of insulin secretion in thalassemic patients may develop earlier than insulin resistance, and then be accompanied by insulin resistance. Increasing insulin resistance with age and the occurrence of additional factors could lead to detoriation of glucose metabolism.
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Lady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, IndiaLady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, India
Chandra, Jagdish
Parakh, Nupur
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Lady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, IndiaLady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, India
Parakh, Nupur
Sidharth
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Lady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, IndiaLady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, India
Sidharth
Singh, Neha
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Lady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, IndiaLady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, India
Singh, Neha
Sharma, Sunita
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Lady Hardinge Med Coll & Associated Kalawati Sara, Dept Pathol, New Delhi, IndiaLady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, India
Sharma, Sunita
Goel, Manish
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Lady Hardinge Med Coll & Associated Kalawati Sara, Dept Community Med, New Delhi, IndiaLady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, India
Goel, Manish
Pemde, Harish
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Lady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, IndiaLady Hardinge Med Coll & Associated Kalawati Sara, Dept Pediat, Div Pediat Hematol, New Delhi, India
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Chiang Mai Univ, Fac Med, Dept Internal Med, Div Hematol, 110 Inthavarorose Rd, Chiang Mai 50200, ThailandChiang Mai Univ, Fac Med, Dept Internal Med, Div Hematol, 110 Inthavarorose Rd, Chiang Mai 50200, Thailand