Abstract | OBJECTIVE: PATIENTS AND METHODS: Forty LGA infants (20 LGA born from diabetic mothers and 20 LGA born from non-diabetic mothers) and 34 appropriate for gestational age (AGA) infants were recruited. Hyperinsulinism and insulin resistance was evaluated using the homeostasis model assessment (HOMA-IR), fasting glucose-to- insulin ratio (FGIR), quantitative insulin-sensitivity check index (QUICK-I) from fasting samples. Plasma adiponectin and vaspin levels were determined by radioimmunoassay. Determination of visfatin and apelin levels was performed by enzyme immunoassay. RESULTS: HOMA-IR, apelin and visfatin levels (p<0.001, p<0.001, p<0.001, respectively) were significantly elevated and adiponectin levels, FGIR and QUICK-I values. (p<0.001, p<0.001, p<0.05, respectively) were significantly lower in the LGA group. Vaspin levels were higher in the LGA group than AGA neonates without a significance. The LGA infants with diabetic mother had significantly higher visfatin, apelin, HOMA-IR values, fasting insulin levels and significantly lower adiponectin, FGIR, QUICK-I values. Apelin and visfatin were correlated positively, and adiponectin was correlated negatively with birthweight, HOMA-IR values and fasting insulin levels. CONCLUSION:
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Authors | Ferhat Cekmez, Fuat Emre Canpolat, Ozgur Pirgon, Merih Çetinkaya, Secil Aydinoz, Selami Suleymanoglu, Osman Metin Ipcioglu, Serdar Umit Sarici |
Journal | Cytokine
(Cytokine)
Vol. 56
Issue 2
Pg. 387-91
(Nov 2011)
ISSN: 1096-0023 [Electronic] England |
PMID | 21742512
(Publication Type: Journal Article)
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Copyright | Copyright © 2011 Elsevier Ltd. All rights reserved. |
Chemical References |
- APLN protein, human
- Adiponectin
- Apelin
- Intercellular Signaling Peptides and Proteins
- SERPINA12 protein, human
- Serpins
- Nicotinamide Phosphoribosyltransferase
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Topics |
- Adiponectin
(blood)
- Apelin
- Female
- Humans
- Infant, Newborn
- Insulin Resistance
- Intercellular Signaling Peptides and Proteins
(blood)
- Male
- Nicotinamide Phosphoribosyltransferase
(blood)
- Serpins
(blood)
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