C-reactive protein gene variants associated with recurrent pregnancy loss independent of CRP serum levels: a case-control study

dc.contributor.authork Ahmad, Salma
dc.contributor.authorMahmood, Naeema
dc.contributor.authorH Malalla, Zainab
dc.contributor.authorM Alsobyani, Fanar
dc.contributor.authorS Al-Kiyumi, Israa
dc.contributor.authorY Almawi, Wassim
dc.date.accessioned2022-03-18T11:24:16Z
dc.date.accessioned2023-08-19T08:55:43Z
dc.date.available2022-03-18T11:24:16Z
dc.date.available2023-08-19T08:55:43Z
dc.date.issued2015
dc.description.abstractThe aim of this study is to investigate the association of recurrent pregnancy loss (RPL) with altered C-reactive protein (CRP) serum levels, and genetic variation in CRP gene. This was a retrospective case–control study, involving 275 women with three or more consecutive pregnancy losses, and 290 age-matched control women, who were recruited from outpatient obstetrics/gynecology clinics. CRP serum levels (hs-CRP) were determined by latex-enhanced nephelometry, and CRP genotyping was done by allelic discrimination. Mean serum CRP levels were higher in RPL cases than in control women, and carriage of the (minor) T allele of rs2794520 was associated with significant increase in CRP levels (P = 0.017).en_US
dc.identifier.citationAhmed, S. K., Mahmood, N., Malalla, Z. H., Alsobyani, F. M., Al-Kiyumi, I. S., & Almawi, W. Y. (2015). C-reactive protein gene variants associated with recurrent pregnancy loss independent of CRP serum levels: a case-control study. Gene, 569(1), 136-140.en_US
dc.identifier.doihttps://doi.org/10.1016/j.gene.2015.05.052
dc.identifier.urihttps://edms.wexl.in/handle/1/2963
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectGeneen_US
dc.subjectGynecologyen_US
dc.subjectPregnancyen_US
dc.subjectSerumen_US
dc.titleC-reactive protein gene variants associated with recurrent pregnancy loss independent of CRP serum levels: a case-control studyen_US
dc.title.alternativeGeneen_US
dc.typeArticleen_US

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