Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1782240253631791104 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3414774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT tennekoonkamanihemamala leprc668agpolymorphisminacohortofsrilankanwomenwithpreeclampsiapregnancyinducedhypertensionacasecontrolstudy AT indikawijesekaraliyanage leprc668agpolymorphisminacohortofsrilankanwomenwithpreeclampsiapregnancyinducedhypertensionacasecontrolstudy AT sugathadasarohan leprc668agpolymorphisminacohortofsrilankanwomenwithpreeclampsiapregnancyinducedhypertensionacasecontrolstudy AT karunanayakeerichamilton leprc668agpolymorphisminacohortofsrilankanwomenwithpreeclampsiapregnancyinducedhypertensionacasecontrolstudy AT kumarasirijayalath leprc668agpolymorphisminacohortofsrilankanwomenwithpreeclampsiapregnancyinducedhypertensionacasecontrolstudy AT wijesunderaajita leprc668agpolymorphisminacohortofsrilankanwomenwithpreeclampsiapregnancyinducedhypertensionacasecontrolstudy |