INSULIN-LIKE GROWTH-FACTOR-I, ITS BINDING-PROTEIN-1 AND BINDING-PROTEIN-3, AND GROWTH-HORMONE BINDING-PROTEIN IN CHILDREN AND ADOLESCENTS WITH INSULIN-DEPENDENT DIABETES-MELLITUS - CLINICAL IMPLICATIONS
Mt. Munoz et al., INSULIN-LIKE GROWTH-FACTOR-I, ITS BINDING-PROTEIN-1 AND BINDING-PROTEIN-3, AND GROWTH-HORMONE BINDING-PROTEIN IN CHILDREN AND ADOLESCENTS WITH INSULIN-DEPENDENT DIABETES-MELLITUS - CLINICAL IMPLICATIONS, Pediatric research, 39(6), 1996, pp. 992-998
Values of IGF-I after extraction, its binding proteins, and the high a
ffinity GH-binding protein (BP) are not well established in pediatric
patients with insulin-dependent diabetes mellitus (IDDM). We report da
ta for IGF-I, IGFBP-1 and -3, and GHBP in 92 Spanish children with IDD
M, separated according to pubertal stage: prepubertal (n = 49); pubert
al onset (n = 17); mid-puberty (n = 17), and complete puberty (n = 9),
as well as to metabolic control (HbA(1) < 9% or greater than or equal
to 9%). IGF-I levels in IDDM patients increased throughout developmen
t (p < 0.001), but were diminished at even, developmental stage when c
ompared with matched control subjects. IGF-I concentrations showed a n
egative correlation with the degree of metabolic control, in particula
r during the prepubertal stage of development. A negative correlation
(r = -0.22; p < 0.005) between IGF-I concentrations and HbA(1) was fou
nd. Serum IGFBP-1 levels diminish during maturation in diabetic patien
ts (p < 0.001), However, IDDM patients have significantly higher level
s of IGFBP-1 than control subjects at every stage of development, and
IDDM patients with inadequate metabolic control exhibit even greater d
ifferences when compared with matched control subjects. A positive cor
relation (r = 0.22; p < 0.005) between IGFBP-1 concentrations and HbA(
1) was found. IGFBP-3 serum levels were similar to those observed in n
ormal subjects, and no correlation was observed in relation to the met
abolic control, In IDDM patients, GHBP levels change significantly dur
ing maturation, as they do in normal control subjects; however, signif
icantly lower GHBP levels were found in prepubertal and pubertal IDDM
patients. GHBP levels were independent of metabolic control, although
a tendency reward lower levels of GHBP was seen when HbA, levels incre
ased. We suggest that a partial GH resistance syndrome exists in IDDM
patients, and this may be related to the metabolic control. Hence, the
biochemical markers measured here may be of value in evaluating the s
maller pubertal growth spurt in diabetic patients.