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1.
BJOG ; 125(9): 1127-1134, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-29377552

RESUMEN

OBJECTIVE: Determine associations of cardiorespiratory fitness, exercise systolic blood pressure (SBP) and heart rate recovery (HRR) following a maximal exercise test performed years preceding pregnancy with odds of preterm birth (PTB; <37 weeks' gestation) and small for gestational age (SGA; birthweight <10th percentile) delivery. DESIGN: Prospective, longitudinal. SETTING: Multi-site, observational cohort study initially consisting of 2787 black and white women aged 18-30 at baseline (1985-86) and followed for 25 years (Y25; 2010-2011). POPULATION: 768 nulliparous women at baseline who reported ≥1 live birth by the Y25 exam. METHODS: We used Poisson regression to determine associations of exposures with PTB/SGA. MAIN OUTCOME MEASURES: PTB and/or SGA births. RESULTS: Women with PTB (n = 143) and/or SGA (n = 88) were younger, had completed fewer years of education and were more likely to be black versus women without PTB/SGA (n = 546). Women with PTB/SGA had lower fitness (501 ± 9 versus 535 ± 6 seconds, P < 0.002) and higher submaximal SBP than women without PTB/SGA (144 ± 1 versus 142 ± 1 mmHg, P < 0.04). After adjustment, no exercise test variables were associated with PTB/SGA, though the association with HRR and submaximal SBP approached significance in the subset of women who completed the exercise test <5 years before the index birth. CONCLUSIONS: Neither fitness nor haemodynamic responses to exercise a median of 5 years preceding pregnancy, were associated with PTB/SGA. These findings indicate excess likelihood of PTB/SGA is not detectable by low fitness or exercise haemodynamic responses 5 years preceding pregnancy, but exercise testing, especially HRR and submaximal SBP, may be more useful when conducted closer to the onset of pregnancy. TWEETABLE ABSTRACT: Exercise testing conducted >5 years before pregnancy may not detect women likely to have PTB/SGA.


Asunto(s)
Capacidad Cardiovascular/fisiología , Enfermedad de la Arteria Coronaria/etiología , Ejercicio Físico/fisiología , Hemodinámica/fisiología , Complicaciones Cardiovasculares del Embarazo/etiología , Nacimiento Prematuro/etiología , Adolescente , Adulto , Femenino , Humanos , Recién Nacido , Recién Nacido Pequeño para la Edad Gestacional , Estudios Longitudinales , Paridad , Distribución de Poisson , Embarazo , Resultado del Embarazo , Estudios Prospectivos , Análisis de Regresión , Factores de Riesgo , Adulto Joven
2.
Int J STD AIDS ; 20(1): 39-45, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19103892

RESUMEN

The relationships between hygiene, sexual behaviour and HIV infection are poorly understood. We examine these relationships in Indian truck drivers, a group at high risk for HIV infection. Truck drivers (n = 189) were recruited into an integrated HIV and hygiene Information Motivation (IM) programme. Sociodemographic characteristics, sexual and hygiene behaviour and HIV prevalence were determined. Multivariate logistic regression and linear generalized estimating equation models were utilized. At baseline, 2.1% of drivers were HIV infected and 34% who reported having contact with female sex workers (FSWs) had contact within the previous six months. Those who washed their hands postdefecation were less likely to report genital symptoms (OR 0.02; P = 0.01) and have sex with an FSW (OR [odds ratio] 0.21; P = 0.05). After an IM intervention, there were no changes in sexual risk-taking behaviour (coefficient -0.15 to -0.02; P = 0.13-0.75); however, hygiene behaviour improved from baseline (coefficient 0.09-0.31; P < 0.01 to P = 0.03). Personal hygiene habits, like handwashing, seem to be a modifiable behaviour after a modest intervention, whereas HIV risk-taking behaviour was not. The association between hygiene and HIV risk-taking suggests the need for further evaluation of the relationship and that of other hygiene practices in high-risk men in India.


Asunto(s)
Infecciones por VIH/epidemiología , Higiene , Asunción de Riesgos , Conducta Sexual , Transportes , Adulto , Femenino , Infecciones por VIH/prevención & control , VIH-1 , Desinfección de las Manos/métodos , Conocimientos, Actitudes y Práctica en Salud , Encuestas Epidemiológicas , Humanos , India , Entrevistas como Asunto , Masculino , Prevalencia , Recursos Humanos
3.
J Immunol ; 165(8): 4710-7, 2000 Oct 15.
Artículo en Inglés | MEDLINE | ID: mdl-11035115

RESUMEN

Dendritic cells (DC) are the major APCs involved in naive T cell activation making them prime targets of vaccine research. We observed that mRNA was efficiently transfected, resulting in superior translation in DC compared with other professional APCs. A single stimulation of T cells by HIV gag-encoded mRNA-transfected DC in vitro resulted in primary CD4(+) and CD8(+) T cell immune responses at frequencies of Ag-specific cells (5-12.5%) similar to primary immune responses observed in vivo in murine models. Additionally, mRNA transfection also delivered a maturation signal to DC. Our results demonstrated that mRNA-mediated delivery of encoded Ag to DC induced potent primary T cell responses in vitro. mRNA transfection of DC, which mediated efficient delivery of antigenic peptides to MHC class I and II molecules, as well as delivering a maturation signal to DC, has the potential to be a potent and effective anti-HIV T cell-activating vaccine.


Asunto(s)
Células Dendríticas/metabolismo , Productos del Gen gag/genética , VIH/genética , Antígenos de Histocompatibilidad Clase II/metabolismo , Antígenos de Histocompatibilidad Clase I/metabolismo , ARN Mensajero/genética , Subgrupos de Linfocitos T/inmunología , Transfección , Presentación de Antígeno/genética , Linfocitos T CD4-Positivos/inmunología , Linfocitos T CD8-positivos/inmunología , Diferenciación Celular/genética , Diferenciación Celular/inmunología , Células Cultivadas , Citotoxicidad Inmunológica/genética , Células Dendríticas/citología , Células Dendríticas/inmunología , Células Dendríticas/virología , Productos del Gen gag/biosíntesis , Productos del Gen gag/metabolismo , Genes Reporteros/inmunología , Humanos , Memoria Inmunológica/genética , ARN Mensajero/farmacología , ARN Viral/genética , Linfocitos T Citotóxicos/inmunología
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