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Developmental variations in plasma leptin, leptin soluble receptor and their molar ratio in healthy infants

BACKGROUND: Leptin and its soluble receptor (sOB-R) are important to regulation of body composition but there are no data on the developmental variations in these plasma variables and their relationship with body composition measurements, METHODS: Weight, length, and body composition (bone, fat and...

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Autores principales: Koo, Winston WK, Hammami, Mouhanad, Hockman, Elaine M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1894811/
https://www.ncbi.nlm.nih.gov/pubmed/17547758
http://dx.doi.org/10.1186/1475-2891-6-11
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author Koo, Winston WK
Hammami, Mouhanad
Hockman, Elaine M
author_facet Koo, Winston WK
Hammami, Mouhanad
Hockman, Elaine M
author_sort Koo, Winston WK
collection PubMed
description BACKGROUND: Leptin and its soluble receptor (sOB-R) are important to regulation of body composition but there are no data on the developmental variations in these plasma variables and their relationship with body composition measurements, METHODS: Weight, length, and body composition (bone, fat and lean mass) by dual energy absorptiometry, and plasma variables were measured in healthy infants at 2, 4, 8 and 12 months. RESULTS: 15 whites and 29 African Americans (21 males and 23 females) with mean birth weight 3357 +/- 45 (SEM) g and gestation of 39.3 +/- 0.17 weeks were studied. The overall Z score for weight, length and weight for length during the study were 0.00 +/- 0.15, -0.08 +/- 0.11 and 0.12 +/- 0.14 respectively. With increasing age, plasma leptin (1.0 to 18.2, median 5.5 ng/mL) and sOB-R:leptin molar ratio (10.1 to 247.4, median 59.9) were lowered (r = -0.47, p < 0.01; and r = -0.37, p < 0.05 respectively), best predicted by weight Z score and percentage of fat mass, and higher in African American and female. Presence of body composition measurements eliminated the race and gender effect on the plasma variables. Plasma sOB-R (49.5 to 173.9, median 81.3 ng/mL) did not change significantly with age and was correlated and predicted only by body composition measurements. CONCLUSION: In healthy growing infants, plasma leptin but not sOB-R decreases with age. Gender, race and anthropometric measurements are additional physiological determinants predictive of plasma leptin and the receptor:ligand ratio. However, body composition is the only variable that can predict plasma leptin and its soluble receptor and the receptor: ligand ratio; and body composition measurements eliminated the race and gender effect on these plasma variables.
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spelling pubmed-18948112007-06-20 Developmental variations in plasma leptin, leptin soluble receptor and their molar ratio in healthy infants Koo, Winston WK Hammami, Mouhanad Hockman, Elaine M Nutr J Research BACKGROUND: Leptin and its soluble receptor (sOB-R) are important to regulation of body composition but there are no data on the developmental variations in these plasma variables and their relationship with body composition measurements, METHODS: Weight, length, and body composition (bone, fat and lean mass) by dual energy absorptiometry, and plasma variables were measured in healthy infants at 2, 4, 8 and 12 months. RESULTS: 15 whites and 29 African Americans (21 males and 23 females) with mean birth weight 3357 +/- 45 (SEM) g and gestation of 39.3 +/- 0.17 weeks were studied. The overall Z score for weight, length and weight for length during the study were 0.00 +/- 0.15, -0.08 +/- 0.11 and 0.12 +/- 0.14 respectively. With increasing age, plasma leptin (1.0 to 18.2, median 5.5 ng/mL) and sOB-R:leptin molar ratio (10.1 to 247.4, median 59.9) were lowered (r = -0.47, p < 0.01; and r = -0.37, p < 0.05 respectively), best predicted by weight Z score and percentage of fat mass, and higher in African American and female. Presence of body composition measurements eliminated the race and gender effect on the plasma variables. Plasma sOB-R (49.5 to 173.9, median 81.3 ng/mL) did not change significantly with age and was correlated and predicted only by body composition measurements. CONCLUSION: In healthy growing infants, plasma leptin but not sOB-R decreases with age. Gender, race and anthropometric measurements are additional physiological determinants predictive of plasma leptin and the receptor:ligand ratio. However, body composition is the only variable that can predict plasma leptin and its soluble receptor and the receptor: ligand ratio; and body composition measurements eliminated the race and gender effect on these plasma variables. BioMed Central 2007-06-04 /pmc/articles/PMC1894811/ /pubmed/17547758 http://dx.doi.org/10.1186/1475-2891-6-11 Text en Copyright © 2007 Koo et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Koo, Winston WK
Hammami, Mouhanad
Hockman, Elaine M
Developmental variations in plasma leptin, leptin soluble receptor and their molar ratio in healthy infants
title Developmental variations in plasma leptin, leptin soluble receptor and their molar ratio in healthy infants
title_full Developmental variations in plasma leptin, leptin soluble receptor and their molar ratio in healthy infants
title_fullStr Developmental variations in plasma leptin, leptin soluble receptor and their molar ratio in healthy infants
title_full_unstemmed Developmental variations in plasma leptin, leptin soluble receptor and their molar ratio in healthy infants
title_short Developmental variations in plasma leptin, leptin soluble receptor and their molar ratio in healthy infants
title_sort developmental variations in plasma leptin, leptin soluble receptor and their molar ratio in healthy infants
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1894811/
https://www.ncbi.nlm.nih.gov/pubmed/17547758
http://dx.doi.org/10.1186/1475-2891-6-11
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