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Combined association of maternal and paternal family history of diabetes with plasma leptin and adiponectin in overweight Hispanic children

AIMS: To investigate the importance of a maternal and paternal family history of Type 2 diabetes and their combined association with plasma leptin and adiponectin levels in overweight Latino children with a family history of Type 2 diabetes (T2DM). METHODS: This cross-sectional study investigated th...

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Autores principales: Koebnick, C, Kelly, L A, Lane, C J, Roberts, C K, Shaibi, G Q, Toledo-Corral, C M, Davis, J N, Weigensberg, M J, Goran, M I
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613241/
https://www.ncbi.nlm.nih.gov/pubmed/19183309
http://dx.doi.org/10.1111/j.1464-5491.2008.02537.x
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author Koebnick, C
Kelly, L A
Lane, C J
Roberts, C K
Shaibi, G Q
Toledo-Corral, C M
Davis, J N
Weigensberg, M J
Goran, M I
author_facet Koebnick, C
Kelly, L A
Lane, C J
Roberts, C K
Shaibi, G Q
Toledo-Corral, C M
Davis, J N
Weigensberg, M J
Goran, M I
author_sort Koebnick, C
collection PubMed
description AIMS: To investigate the importance of a maternal and paternal family history of Type 2 diabetes and their combined association with plasma leptin and adiponectin levels in overweight Latino children with a family history of Type 2 diabetes (T2DM). METHODS: This cross-sectional study investigated the combined association of a maternal and paternal family history of T2DM with leptin and adiponectin in 175 overweight Latino children (age 11.1 ± 1.7 years). All subjects had a family history of T2DM. Plasma adiponectin and leptin levels, body fat measured by dual-energy X-ray absorptiometry, Tanner stage, age and insulin sensitivity were assessed. RESULTS: After adjustment for age, gestational diabetes, insulin sensitivity and body fat, a combined maternal and paternal family history of T2DM was associated with higher leptin concentrations (P = 0.004) compared with a maternal or paternal family history alone. This association was most pronounced at Tanner stage 1 (P for interaction family history × tanner stage = 0.022). The presence of a combined maternal and paternal family history of T2DM accounted for 4% (P = 0.003) of the variation in leptin concentrations. No such combined association was observed for adiponectin levels. CONCLUSIONS: Maternal and paternal family history of T2DM may have an additive impact on leptin, but not on adiponectin levels independent of adiposity and insulin sensitivity in overweight Latino children. This may contribute to a further clinically relevant deterioration of metabolic health in this population. Diabet. Med. 25, 1043–1048 (2008)
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spelling pubmed-26132412009-01-27 Combined association of maternal and paternal family history of diabetes with plasma leptin and adiponectin in overweight Hispanic children Koebnick, C Kelly, L A Lane, C J Roberts, C K Shaibi, G Q Toledo-Corral, C M Davis, J N Weigensberg, M J Goran, M I Diabet Med Original Article: Metabolism AIMS: To investigate the importance of a maternal and paternal family history of Type 2 diabetes and their combined association with plasma leptin and adiponectin levels in overweight Latino children with a family history of Type 2 diabetes (T2DM). METHODS: This cross-sectional study investigated the combined association of a maternal and paternal family history of T2DM with leptin and adiponectin in 175 overweight Latino children (age 11.1 ± 1.7 years). All subjects had a family history of T2DM. Plasma adiponectin and leptin levels, body fat measured by dual-energy X-ray absorptiometry, Tanner stage, age and insulin sensitivity were assessed. RESULTS: After adjustment for age, gestational diabetes, insulin sensitivity and body fat, a combined maternal and paternal family history of T2DM was associated with higher leptin concentrations (P = 0.004) compared with a maternal or paternal family history alone. This association was most pronounced at Tanner stage 1 (P for interaction family history × tanner stage = 0.022). The presence of a combined maternal and paternal family history of T2DM accounted for 4% (P = 0.003) of the variation in leptin concentrations. No such combined association was observed for adiponectin levels. CONCLUSIONS: Maternal and paternal family history of T2DM may have an additive impact on leptin, but not on adiponectin levels independent of adiposity and insulin sensitivity in overweight Latino children. This may contribute to a further clinically relevant deterioration of metabolic health in this population. Diabet. Med. 25, 1043–1048 (2008) Blackwell Publishing Ltd 2008-09 /pmc/articles/PMC2613241/ /pubmed/19183309 http://dx.doi.org/10.1111/j.1464-5491.2008.02537.x Text en © 2008 The Authors. Journal compilation © 2008 Diabetes UK.
spellingShingle Original Article: Metabolism
Koebnick, C
Kelly, L A
Lane, C J
Roberts, C K
Shaibi, G Q
Toledo-Corral, C M
Davis, J N
Weigensberg, M J
Goran, M I
Combined association of maternal and paternal family history of diabetes with plasma leptin and adiponectin in overweight Hispanic children
title Combined association of maternal and paternal family history of diabetes with plasma leptin and adiponectin in overweight Hispanic children
title_full Combined association of maternal and paternal family history of diabetes with plasma leptin and adiponectin in overweight Hispanic children
title_fullStr Combined association of maternal and paternal family history of diabetes with plasma leptin and adiponectin in overweight Hispanic children
title_full_unstemmed Combined association of maternal and paternal family history of diabetes with plasma leptin and adiponectin in overweight Hispanic children
title_short Combined association of maternal and paternal family history of diabetes with plasma leptin and adiponectin in overweight Hispanic children
title_sort combined association of maternal and paternal family history of diabetes with plasma leptin and adiponectin in overweight hispanic children
topic Original Article: Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613241/
https://www.ncbi.nlm.nih.gov/pubmed/19183309
http://dx.doi.org/10.1111/j.1464-5491.2008.02537.x
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