ESPE Abstracts (2023) 97 RFC11.2

ESPE2023 Rapid Free Communications GH and IGFs (6 abstracts)

Are pappalysins and stanniocalcins involved in modifying the bioavailability of IGF-I in children with onset of type 1 diabetes mellitus?

Maria Güemes 1 , Sandra Canelles 1 , Álvaro Martín-Rivada 1 , Beatriz Corredor 2 , Vicente Barrios 1 & Jesús Argente 1,3,4,5


1Hospital Universitario Infantil Niño Jesús, Madrid, Spain. 2Hospital Universitario de Toledo, Toledo, Spain. 3Universidad Autónoma de Madrid, Madrid, Spain. 4CIBER de Obesidad y Nutrición (CIBEROBN). Instituto de Salud Carlos III, Madrid, Spain. 5IMDEA Alimentación/IMDEA Food, Madrid, Spain


Introduction: Both poor and optimal metabolic control of type 1 diabetes mellitus (T1DM) in children can impact longitudinal growth. A decrease in insulin-like growth factor (IGF)-I and its binding protein 3 (IGFBP3) has been described in these patients. New growth regulatory factors [pappalysins (PAPP-As) and stanniocalcins (STCs)] could modulate the bioavailability of IGFs by regulating the concentrations of intact and free IGFBPs.

Aims: To study the effect of insulin treatment on serum concentrations of pappalysins and stanniocalcins and the possible correlation with markers of the growth axis, beta-cell insulin reserve, auxology and nutrition in children with T1DM.

Methods: 47 patients were included (59.5% females), with diabetes onset at age 9.08 +/- 5.8 years (median +/- interquartile range). Blood was extracted and anthropometric data collected at onset, 6 and 12 months. Serum concentrations were obtained using ELISAs, except PAPP-A2 (chemiluminescence immunoassay); all were standardized for age, sex, and pubertal development.

Results: Table 1 shows the results of the serum concentrations. At 6 and 12 months after T1DM onset, there was improvement in the metabolic control [decrease in HbA1c at 12 months -3.66 IC95%(-4.81,-2.05), P=0.001], certain nutritional markers [30.91 IC95%(0.36,61.47) P<0.05 for transferrin], body mass index SDS and height SDS (not statistically significant).

Analyte (SD) Onset [median (IQR)] 6 months [median (IQR)] 12 months [median (IQR)]
Total IGF-I -1.20 (-1.56,-0.50) -0.04 (-0.77,0.3)*** -0.53 (-0.89,0.25)#
Free IGF-I -1.59 (-1.78,-1.18) -1.56 (-1.8-0.97) -1.29 (-1.8,0.65)
Total IGF-II 0.54 (0.01,1.68) 1.08 (0.39,1.63) 1.71 (1.08,2.41)#
ALS -0.94 (-1.59, 0.15) 0.53 (-0.24,1.18)*** 0.41 (0.11,1.01)##
IGFBP-2 -0.48 (-1.42,0.49) -0.83 (-1.43,-0.07) -0.47 (-1.19,0.12)
Total IGFBP3 0.15 (-0.71,0.88) 0.24 (-0.32,0.44) 0.34 (-0.13,0.73)
Intact IGFBP3 -1.07 (-1.89,-0.62) -0.22 (-0.97,0.11)*** -0.09 (-1.01,0.15)##
Total IGFBP4 -0.24 (-0.64,0.24) -0.16 (-0.58,0.97) 0.98 (0.45,1.32)###
Intact IGFBP4 -0.72 (-1.04,-0.23) -0.47(-0.73,0.45) -0.13 (-0.47,0.65)
IGFBP5 -0.93 (-1.35,-0.03) 0.45 (-1.8,-0.97)*** 1.95 (0.72,2.42)###
STC1 -1.23 (-1.56,-0.84) -1.19 (-1.37,-0.94) -1.26 (-1.35,-0.85)
STC2 -1.31 (-1.97,-0.39) 0.07 (-0.37,0.69)*** 0.52 (-0.76,0.90)###
PAPP-A 0.63 (-0.08,1.33) 0.80 (-0.3,1.27) 0.93 (0.76,1.92)
PAPPA-A2 1.05 (0.68,1.63) 0.49 (-0.07,0.92)*** 0.13 (-0.16,0.52)###
ANOVA p value of onset versus 6 months (*P<0.05, ** P<0.01, ***P<0.001) and onset versus 12 months (#P<0.05, ## P<0.01, ###P<0.001)

Conclusions: Our preliminary results indicate that implementation of insulin treatment after T1DM onset modifies various members of the circulating IGF system, including those of PAPPA-A2 and STC2. How these modifications correlate with linear growth are under investigation.

Volume 97

61st Annual ESPE (ESPE 2023)

The Hague, Netherlands
21 Sep 2023 - 23 Sep 2023

European Society for Paediatric Endocrinology 

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