Diabetes Care, Vol 18, Issue 1 47-55, Copyright © 1995 by American Diabetes Association
Pentamidine-induced derangements of glucose homeostasis. Determinant roles of renal failure and drug accumulation. A study of 128 patients
R Assan, C Perronne, D Assan, L Chotard, C Mayaud, S Matheron and D Zucman
Service de Diabetologie, Hopital Bichat, Paris, France.
OBJECTIVE--To assess the prevalence, presentation, and risk factors of
pentamidine-induced dysglycemia. RESEARCH DESIGN AND METHODS--Blood glucose
values were screened in 244 consecutive immunocompromised patients with
Pneumocystis carinii pneumonia: 116 being treated with cotrimoxazole and
128 others with pentamidine. RESULTS--Two cotrimoxazole patients developed
diabetes as a result of necrotizing pancreatitis (1.7%); the others
remained euglycemic. Forty-eight pentamidine-treated patients (38.5%)
developed severe glucose homeostasis disorders: hypoglycemia in 7,
hypoglycemia and then diabetes in 18, and diabetes alone in 23 (P <
0.001 vs. the cotrimoxazole group). Hypoglycemia was early, sudden, often
recurrent, and life-threatening, associated with inappropriately high
insulin levels in plasma; the B-cell response to stimuli was poor. Of the
41 diabetic patients, 26 required insulin therapy; their plasma C-peptide
levels were lower than normal, and the B-cell secretory responses to
stimuli were poor. Islet cell antibodies, insulin antibodies, and insulitis
were not detected. The pentamidine-treated dysglycemic patients differed
from their euglycemic counterparts by higher pentamidine doses (P <
0.001), higher plasma creatinine levels (P < 0.001), and more severe
anoxia (P < 0.05) and shock (P < 0.001). Most of them had received
pentamidine mesylate parenterally (n = 36; 75%); six others received the
isethionate salt and six exclusively pentamidine aerosols.
CONCLUSIONS--Pentamidine-induced dysglycemic accidents are primarily due to
inappropriate insulin release and toxicity to the islet B-cells. Drug
accumulation due to excessive doses, iterative courses, and/or renal
impairment is the determining risk factor.