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1.
Genes (Basel) ; 11(6)2020 06 26.
Artigo em Inglês | MEDLINE | ID: mdl-32604723

RESUMO

BACKGROUND: So far, numerous meta-analyses have been published regarding the correlation between peroxisome proliferator-activated receptor gamma (PPARG) proline 12 alanine (Pro12Ala) gene polymorphism and chronic kidney disease (CKD); however, the results appear to be contradictory. Hence, this study is formulated with the objective of using existing meta-analysis data together with our research population to study the correlation between PPARG Pro12Ala gene polymorphism and CKD and evaluate whether an accurate result can be obtained. METHODS: First, literature related to CKD and PPARG Pro12Ala available on the PubMed and EMBASE databases up to December 2016 was gathered from 20 publications. Then, the gathered results were combined with our case-control study of 1693 enrolled subjects and a trial sequential analysis (TSA) was performed to verify existing evidence and determine whether a firm conclusion can be drawn. RESULTS: The TSA results showed that the cumulative sample size for the Asian sample was 6078 and was sufficient to support a definite result. The results of this study confirmed that there is no obvious correlation between PPARG Pro12Ala and CKD for Asians (OR = 0.82 (95% CI = 0.66-1.02), I2 = 63.1%), but this was not confirmed for Caucasians. Furthermore, the case-control sample in our study was shown to be the key for reaching this conclusion. CONCLUSIONS: The meta-analysis results of this study suggest no significant correlation between PPARG Pro12Ala gene polymorphism and CKD for Asians after adding our samples, but not for Caucasian.


Assuntos
Estudos de Associação Genética , Predisposição Genética para Doença , PPAR gama/genética , Insuficiência Renal Crônica/genética , Idoso , Povo Asiático/genética , Estudos de Casos e Controles , Feminino , Interação Gene-Ambiente , Humanos , Masculino , Polimorfismo de Nucleotídeo Único/genética , Insuficiência Renal Crônica/epidemiologia , Insuficiência Renal Crônica/patologia , População Branca/genética
2.
IEEE Trans Inf Technol Biomed ; 15(4): 585-93, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21606040

RESUMO

As Internet technologies evolve, their applications have changed various aspects of human life. Here, we attempt to examine their potential impact on services for families with developmentally delayed children. Our research is thus designed to utilize wireless mobile communication technologies, location services, and search technology in an effort to match families of specific needs with potential care providers. Based on the investigation conducted by our counselors, this paper describes a platform for smooth communication between professional communities and families with children with developmental disabilities (CDD). This research also looks into the impact of management of mobile social network services and training on the operation of these services. Interaction opportunities, care, and support to families with CDD are introduced.


Assuntos
Deficiências do Desenvolvimento/terapia , Internet , Apoio Social , Serviço Social/métodos , Adulto , Pré-Escolar , Computadores de Mão , Mineração de Dados , Humanos , Microcomputadores , Pais , Serviço Social/instrumentação , Software , Telecomunicações , Interface Usuário-Computador
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