• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 1
  • Tagged with
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Fatores de risco individuais e familiares no desenvolvimento da pr?-ecl?mpia

Pereira, Flavio Ven?cio Marinho 23 July 2010 (has links)
Made available in DSpace on 2014-12-17T14:13:38Z (GMT). No. of bitstreams: 1 FlavioVMP_TESE.pdf: 2484442 bytes, checksum: a01024c65d8fb94c5394db6d7689663e (MD5) Previous issue date: 2010-07-23 / Preeclampsia is a spectral disease, with different clinical forms which can evolve with severe multisystemic complications. This present study aimed to determine the risk factors associated with preeclampsia (PE); to validate the existence of aggregation of hypertensive disease in families of women with preeclampsia and verify the existence of association between polymorphisms in the VEGF gene and level of VEGF and its soluble receptor (sFlt1). A case-control study was performed (n = 851). Genotyping of VEGF was performed and serum levels of VEGF and sFlt1 were measured by ELISA. It was observed that 38% of mothers (173, 455) of a case of preeclampsia and 30.8% (78 of 361) of controls had history of hypertension (p <0.0001). Similarly, when examining the history of maternal preeclampsia, we observed that 14.6% (48 of 328) of mothers of women with preeclampsia and 9.6% (12 of 294) of mothers of controls had a history of preeclampsia (p = 0.0001). As for maternal history of preeclampsia, we found that 5.1% (15 of 295) of cases and 3.6% (7 of 314) of controls had a history of preeclampsia (p = 0.0568). Sisters of women with preeclampsia also had a history of hypertensive disease in 9% (41 of 455) versus 6.6% (13 of 361), p = 0.002. Similarly when examining the history of preeclampsia in sisters, it was observed that 22.7% (57 of 251) of a sister of case versus 11.4% (26 of 228) of controls had a history of preeclampsia (P = 0.0011). We observed a decrease in free VEGF in the serum of patients (P <0.05) and increased soluble VEGF receptor. There was no association between polymorphisms in the VEGF gene and preeclampsia. The data obtained in this work validate that hypertensive disease in mothers and sisters with preeclampsia are risk factors for preeclampsia. The risk of illness in the family is higher according to disease severity. High incidence of preeclampsia can be assumed by the high incidence of this disease among the controls. Significant differences between the frequency of preeclampsia in mothers of cases and controls indicate familial factors. Work is being conducted with the to eventually perform genome wide association studies to identify susceptibility loci / A pr?-ecl?mpsia ? uma doen?a espectral, com formas distintas, podendo evoluir com complica??es multissist?micas graves. Este presente trabalho teve como objetivos determinar os fatores de risco envolvidos com a pr?-ecl?mpsia (PE); validar a exist?ncia de agrega??o de doen?a hipertensiva em fam?lias de gestantes com pr?ecl?mpsia; verificar a exist?ncia de associa??o entre polimorfismo no gene do VEGF e determinar os n?veis de VEGF e seu receptor sol?vel (sFlt1). Um estudo caso-controle foi realizado (n=851). A genotipagem do VEGF foi realizada e os n?veis s?ricos de VEGF e sFlt1 foram determinados por ELISA. Foi observado que 38 % das m?es (173 de 455) de um caso de pr?-ecl?mpsia e 30.8% (78 de 361) dos controles apresentavam hist?ria de hipertens?o (p<0.0001). De forma que 14.6% (48 de 328) das m?es das gestantes com pr?-ecl?mpsia e 9.6% (12 de 294) das m?es dos controles tinham hist?ria de pr?-ecl?mspia (p=0.0001). Quanto ? hist?ria materna de ecl?mpsia, observou-se que 5.1% (15 de 295) dos casos e 3.6% (7 de 314) dos controles tinham hist?ria de pr?-ecl?mpsia (p=0.0568). Irm?s das gestantes com pr?-ecl?mpsia tinham tamb?m hist?ria de doen?a hipertensiva em 9% (41 de 455), versus 6.6% (13 de 361) dos controles, p=0.002. Da mesma forma ao ser examinada a hist?ria de pr?-ecl?mpsia em irm?s, observou-se que 22.7% (57 de 251) das irm?s dos casos de pr?-ecl?mpsia, versus 11.4% (26 de 228) dos controles apresentavam hist?ria de pr?-ecl?mpsia (P=0.0011). O VEGF livre estava diminu?do no soro dos casos (P<0.05) enquanto que o receptor sol?vel do VEGF estava aumentado. N?o foi observada associa??o entre polimorfismos nos genes do VEGF e pr?-ecl?mpsia. Os dados obtidos neste trabalho validam que doen?a hipertensiva em m?es e irm?s com pr?-ecl?mpsia s?o fatores de risco para pr?-ecl?mpsia. O risco de doen?a na fam?lia ? maior de acordo com a gravidade da doen?a. A hist?ria de pr?-ecl?mpsia elevada em familiares dos controles respectivamente, 9,6% e 11,4%, em m?es e irm?s dos controles demonstram que a pr?-ecl?mpsia ? uma done?a freq?ente nesta popula??o. Trabalho est? sendo conduzido para realizar estudos de varredura ampla do genoma, para permitir identificar loci de susceptibilidade

Page generated in 0.0314 seconds