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LEPR c.668A>G polymorphism in a cohort of Sri Lankan women with pre-eclampsia / pregnancy induced hypertension: a case control study

BACKGROUND: Leptin is known to be elevated in pre-eclampsia/ pregnancy induced hypertension (PE/PIH). However the reports on the association of leptin receptor (LEPR) c.668A>G polymorphism with PE/PIH are inconsistent. FINDINGS: LEPR c.668A>G polymorphism was studied in a cohort of women with...

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Autores principales: Tennekoon, Kamani Hemamala, Indika, Wijesekara Liyanage, Sugathadasa, Rohan, Karunanayake, Eric Hamilton, Kumarasiri, Jayalath, Wijesundera, Ajita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414774/
https://www.ncbi.nlm.nih.gov/pubmed/22713493
http://dx.doi.org/10.1186/1756-0500-5-308
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author Tennekoon, Kamani Hemamala
Indika, Wijesekara Liyanage
Sugathadasa, Rohan
Karunanayake, Eric Hamilton
Kumarasiri, Jayalath
Wijesundera, Ajita
author_facet Tennekoon, Kamani Hemamala
Indika, Wijesekara Liyanage
Sugathadasa, Rohan
Karunanayake, Eric Hamilton
Kumarasiri, Jayalath
Wijesundera, Ajita
author_sort Tennekoon, Kamani Hemamala
collection PubMed
description BACKGROUND: Leptin is known to be elevated in pre-eclampsia/ pregnancy induced hypertension (PE/PIH). However the reports on the association of leptin receptor (LEPR) c.668A>G polymorphism with PE/PIH are inconsistent. FINDINGS: LEPR c.668A>G polymorphism was studied in a cohort of women with PE/PIH (N = 61) and normotensive pregnancies (N = 40) by polymerase chain reaction / restriction fragment length polymorphism. Genotype and allele frequencies were in Hardy-Weinberg equilibrium within both groups (Chi square test). Allele and genotype frequencies were not significantly different between PE/PIH and normotensive pregnancies (Chi square test). Leptin levels (Kruskal Wallis analysis of variance) and leptin/body mass index (one way analysis of variance) were not significantly different between genotypes within each group. However, leptin (Mann Whitney U test) and leptin normalised to body mass index (unpaired t test) were significantly higher in PE/PIH women homozygous and heterozygous for the G668 allele than in respective normotensives. CONCLUSIONS: Whether the leptin receptor c.668A>G polymorphism increases the risk of developing PE/PIH in Sri Lankan women remains inconclusive in view of the smaller sample studied. However leptin levels in PE/PIH appeared to be modulated by this polymorphism.
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spelling pubmed-34147742012-08-10 LEPR c.668A>G polymorphism in a cohort of Sri Lankan women with pre-eclampsia / pregnancy induced hypertension: a case control study Tennekoon, Kamani Hemamala Indika, Wijesekara Liyanage Sugathadasa, Rohan Karunanayake, Eric Hamilton Kumarasiri, Jayalath Wijesundera, Ajita BMC Res Notes Short Report BACKGROUND: Leptin is known to be elevated in pre-eclampsia/ pregnancy induced hypertension (PE/PIH). However the reports on the association of leptin receptor (LEPR) c.668A>G polymorphism with PE/PIH are inconsistent. FINDINGS: LEPR c.668A>G polymorphism was studied in a cohort of women with PE/PIH (N = 61) and normotensive pregnancies (N = 40) by polymerase chain reaction / restriction fragment length polymorphism. Genotype and allele frequencies were in Hardy-Weinberg equilibrium within both groups (Chi square test). Allele and genotype frequencies were not significantly different between PE/PIH and normotensive pregnancies (Chi square test). Leptin levels (Kruskal Wallis analysis of variance) and leptin/body mass index (one way analysis of variance) were not significantly different between genotypes within each group. However, leptin (Mann Whitney U test) and leptin normalised to body mass index (unpaired t test) were significantly higher in PE/PIH women homozygous and heterozygous for the G668 allele than in respective normotensives. CONCLUSIONS: Whether the leptin receptor c.668A>G polymorphism increases the risk of developing PE/PIH in Sri Lankan women remains inconclusive in view of the smaller sample studied. However leptin levels in PE/PIH appeared to be modulated by this polymorphism. BioMed Central 2012-06-19 /pmc/articles/PMC3414774/ /pubmed/22713493 http://dx.doi.org/10.1186/1756-0500-5-308 Text en Copyright ©2012 Tennekoon 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 Short Report
Tennekoon, Kamani Hemamala
Indika, Wijesekara Liyanage
Sugathadasa, Rohan
Karunanayake, Eric Hamilton
Kumarasiri, Jayalath
Wijesundera, Ajita
LEPR c.668A>G polymorphism in a cohort of Sri Lankan women with pre-eclampsia / pregnancy induced hypertension: a case control study
title LEPR c.668A>G polymorphism in a cohort of Sri Lankan women with pre-eclampsia / pregnancy induced hypertension: a case control study
title_full LEPR c.668A>G polymorphism in a cohort of Sri Lankan women with pre-eclampsia / pregnancy induced hypertension: a case control study
title_fullStr LEPR c.668A>G polymorphism in a cohort of Sri Lankan women with pre-eclampsia / pregnancy induced hypertension: a case control study
title_full_unstemmed LEPR c.668A>G polymorphism in a cohort of Sri Lankan women with pre-eclampsia / pregnancy induced hypertension: a case control study
title_short LEPR c.668A>G polymorphism in a cohort of Sri Lankan women with pre-eclampsia / pregnancy induced hypertension: a case control study
title_sort lepr c.668a>g polymorphism in a cohort of sri lankan women with pre-eclampsia / pregnancy induced hypertension: a case control study
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414774/
https://www.ncbi.nlm.nih.gov/pubmed/22713493
http://dx.doi.org/10.1186/1756-0500-5-308
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