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1.
Singapore Med J ; 57(12): 690-693, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26805669

RESUMO

INTRODUCTION: This study aimed to determine the prevalence of asthma-like symptoms among schoolchildren with low birth weight (LBW), and to compare the lung function of these children with that of children with normal birth weight. METHODS: This was a comparative cross-sectional study. We recruited children aged 8-11 years from eight primary schools in Kota Bharu, Kelantan, Malaysia. The children were divided into two groups: those with LBW (< 2,500 g) and those with normal birth weight (≥ 2,500 g). Parents of the enrolled children were asked to complete a translated version of the International Study of Asthma and Allergies in Childhood questionnaire. Lung function tests, done using a MicroLoop Spirometer, were performed for the children in both groups by a single investigator who was blinded to the children's birth weight. RESULTS: The prevalence of 'ever wheezed' among the children with LBW was 12.9%. This value was significantly higher than that of the children with normal birth weight (7.8%). Forced vital capacity (FVC), forced expiratory volume in one second, and forced expiratory flow when 50% and 75% of the FVC had been exhaled were significantly lower among the children with LBW as compared to the children with normal birth weight. CONCLUSION: LBW is associated with an increased prevalence of asthma-like symptoms and impaired lung function indices later in life. Children born with LBW may need additional follow-up so that future respiratory problems can be detected early.


Assuntos
Asma/epidemiologia , Asma/etiologia , Recém-Nascido de Baixo Peso , Criança , Estudos Transversais , Bases de Dados Factuais , Feminino , Humanos , Malásia/epidemiologia , Masculino , Prevalência , Testes de Função Respiratória , Sons Respiratórios , Instituições Acadêmicas , Espirometria , Inquéritos e Questionários
2.
J Hum Genet ; 48(12): 650-653, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-14618420

RESUMO

Southeast Asian ovalocytosis (SAO) is a red blood cell abnormality common in malaria-endemic regions and caused by a 27 nt deletion of the band 3 protein gene. Since band 3 protein, also known as anion exchanger 1, is expressed in renal distal tubules, the incidence of SAO was examined in distal renal tubular acidosis (dRTA) in Malays in Kelantan, Malaysia. Twenty-two patients with dRTA and 50 healthy volunteers were examined for complication of SAO by both morphological and genetic analyses. SAO was identified in 18 of the 22 dRTA patients (81.8%), but only two of the 50 controls (4%). The incidence of SAO was significantly high in those with dRTA (p<0.001), indicating a dysfunctional role for band 3 protein/anion exchanger 1 in the development of dRTA.


Assuntos
Acidose Tubular Renal/genética , Proteína 1 de Troca de Ânion do Eritrócito/genética , Eliptocitose Hereditária/genética , Acidose Tubular Renal/complicações , Adulto , Criança , Pré-Escolar , Eliptocitose Hereditária/complicações , Eritrócitos/patologia , Feminino , Deleção de Genes , Humanos , Lactente , Malásia , Masculino , Pessoa de Meia-Idade
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