Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: Development Of A Clinical Laboratory Data Base Of Hyper And Hypo Alpha Lipoproteins In Campinas-sp And Neighboring Region
Author: Parra E.S.
De Souza Zago V.H.
Panzoldo N.B.
Alexandre F.
Vendrame F.
De Moura Virginio V.W.
Vieira I.C.
Rodrigues M.S.D.
De Souza Cassol A.
D'Alexandri F.
Castanho V.S.
Nakamura R.
Baracat J.
Danelon M.R.G.
Pozeti R.C.S.
Facin A.C.C.
Da Silva Honorio H.M.
De Cassia Dias Mesquita S.
Da Silva M.J.
Lot M.C.F.
Nunes V.S.
Leanca C.C.
Nakandakare E.R.
Quintao E.C.R.
De Faria E.C.
Abstract: Introduction: The development of research for diagnosis, prevention and treatment of atherosclerotic cardiovascular disease is of utmost importance due to the fact that it is the main cause of morbidity and mortality in Brazil. Objective: To demonstrate the phases of the selection process for candidates with the aim to develop a clinical-laboratorial database of hyper alpha lipoproteinemic patients (hyper A) - high density lipoprotein cholesterol (HDL-C) ≥ 68 mg/dl) and hypo alpha lipoproteinemic patients (hypo A) - HDL-C ≤ 39 mg/dl. Material and methods: The volunteers were contacted after selection of lipid profiles from individuals treated at the Sistema Único de Saúde (SUS), Campinas-SP and neighboring area. Afterwards, the selected patients went through blood collection, clinical examinations and answered questionnaires on dietary frequency and physical activity. After this preliminary evaluation, some individuals were convened to another blood collection and, subsequently, were submitted to an ultrasonographic exam of the carotid arteries. Results: Only 0.6% and 0.3% from 598,288 lipid profiles were selected for hyper A and hypo A groups, respectively, including gender disparity. Lack of effective questionnaires (75%), missing calls (60%) and non-inclusion were the major hindrances in the construction of this database. Discussion: The difficulties to obtain eligible candidates were also due to the low prevalence of both groups hypo A and hyper A and the high prevalence of pathologies that contribute to non-genetic variations of HDL-C. Conclusion: In spite of the obstacles in the development of this database, this study brought about several scientific publications. Furthermore, the development of molecular analyzes and functionality will shortly generate other findings, contributing to the diagnosis and follow-up of HDL dyslipidemias.
Rights: aberto
Identifier DOI: 10.1590/S1676-24442013000100004
Date Issue: 2013
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.