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1.
J Family Med Prim Care ; 10(4): 1773-1779, 2021 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-34123927

RESUMO

CONTEXT: Headaches can negatively impact children's quality of life. Nevertheless, data on the parental awareness of childhood headache is very limited. AIM: The objective was to estimate the prevalence of childhood headaches and parental awareness of headaches among their elementary school children. SETTINGS AND DESIGN: A cross-sectional study was conducted among parents who were shopping in five malls in Riyadh between March and July 2019. METHODS AND MATERIAL: Data were collected using a self-completed questionnaire, which included data on socio-demographic characteristics of the parents and their children, the presence of headache in children, and parental awareness about headache susceptibility, possible causes, associated symptoms, and management. STATISTICAL ANALYSIS USED: Descriptive and inferential statistics were employed as appropriate using the software SPSS. RESULTS: A total of 292 parents were included. The majority were mothers (75.3%) in the age range of 26-45 years (83.2%). Approximately 62.3% of the parents reported headaches in their children. Approximately 47.6% of the headaches were attributed to "the use of electronic devices". The overall parental awareness of headaches was 55.1%, with scores being highest for management questions (67.0%) and lowest for susceptibility questions (45.4%). In a multivariate logistic regression analysis adjusted for socio-demographic characteristics, parental awareness was positively associated with the presence of children with headaches in the family and negatively associated with Saudi nationality of the children. CONCLUSIONS: Parental awareness of childhood headache is insufficient. There is a need to increase the awareness of parents about childhood headaches and the problems associated with heavy electronic device use.

2.
Saudi Med J ; 41(11): 1234-1240, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-33130844

RESUMO

OBJECTIVES: To investigate the relationship between a prostasin gene variations and the development of preeclampsia in a Pakistani female population. Methods: This was a case-control study carried out at University of Karachi, Karachi, Pakistan between May 2018 and 2019. A single nucleotide polymorphism (SNP) at rs12597511 locus was examined with polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) analyses in 76 preeclamptic and 74 normotensive expecting mothers. RESULTS: We observed significantly increased risk of preeclampsia associated with the CC genotype of rs12597511 polymorphism as compared to TT (p less than 0.001, OR=8.08, 95% CI: 1.28-31.19) and TT/TC (p less than 0.001, OR=14.66 and 95% CI: 3.31-65.07) genotypes carriers. Calculation of the allelic distribution revealed a higher frequency of the T allele (82%) among controls; however, the C allele was more prevalent in the preeclamptic group (36%) significantly. CONCLUSION: The significantly higher C allele frequency in the prostasin gene at the rs12597511 locus in the preeclamptic group indicates that the distribution of the C allele of the prostasin gene is a potential risk factor contributing to the development of preeclampsia.


Assuntos
Estudos de Associação Genética , Polimorfismo de Nucleotídeo Único/genética , Pré-Eclâmpsia/genética , Serina Endopeptidases/genética , Estudos de Casos e Controles , Feminino , Frequência do Gene/genética , Humanos , Paquistão , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Pré-Eclâmpsia/etiologia , Gravidez , Risco , Fatores de Risco
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