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1.
Am J Epidemiol ; 188(8): 1420-1433, 2019 08 01.
Artículo en Inglés | MEDLINE | ID: mdl-30927351

RESUMEN

We describe the design, implementation, and results of the Qatar Biobank (QBB) cohort study for the first 10,000 participants. QBB is a prospective, population-based cohort study in Qatar, established in 2012. QBB's primary goal was to establish a cohort accessible to the local and international scientific community, providing adequate health data and biological samples to enable evidence-based research. The study design is based on an agnostic hypothesis, collecting data using questionnaires, biological samples, imaging data, and -omics. QBB aims to recruit 60,000 participants, men and women, adult (aged ≥18 years) Qataris or long-term residents (≥15 years living in Qatar) and follow up with them every 5 years. Currently, QBB has reached 28% (n = 17,065) of the targeted enrollee population and more than 2 million biological samples. QBB is a multinational cohort including 33 different nationalities, with a relatively young population (mean age, 40.5 years) of persons who are highly educated (50% university-educated) and have high monthly incomes. The 4 main noncommunicable diseases found among the QBB population are dyslipidemia, diabetes, hypertension, and asthma with prevalences of 30.1%, 17.4%, 16.8%, and 9.1%, respectively. The QBB repository can provide data and biological samples sufficient to demonstrate valid associations between genetic and/or environmental exposure and disease development to scientists worldwide.


Asunto(s)
Bancos de Muestras Biológicas/organización & administración , Enfermedades no Transmisibles/epidemiología , Proyectos de Investigación , Adulto , Anciano , Biomarcadores , Pesos y Medidas Corporales , Estudios de Cohortes , Femenino , Humanos , Masculino , Persona de Mediana Edad , Prevalencia , Estudios Prospectivos , Qatar/epidemiología , Factores Socioeconómicos
2.
Am J Epidemiol ; 188(1): 141-150, 2019 01 01.
Artículo en Inglés | MEDLINE | ID: mdl-30252047

RESUMEN

Prenatal cadmium exposure has been associated with impaired fetal growth; much less is known about the impact during later childhood on growth and cardiometabolic traits. To elucidate the associations of prenatal cadmium exposure with child growth, adiposity, and cardiometabolic traits in 515 mother-child pairs in the Rhea Mother-Child Study cohort (Heraklion, Greece, 2007-2012), we measured urinary cadmium concentrations during early pregnancy and assessed their associations with repeated weight and height measurements (taken from birth through childhood), waist circumference, skinfold thickness, blood pressure, and serum lipid, leptin, and C-reactive protein levels at age 4 years. Adjusted linear, Poisson, and mixed-effects regression models were used, with interaction terms for child sex and maternal smoking added. Elevated prenatal cadmium levels (third tertile of urinary cadmium concentration (0.571-2.658 µg/L) vs. first (0.058-0.314 µg/L) and second (0.315-0.570 µg/L) tertiles combined) were significantly associated with a slower weight trajectory (per standard deviation score) in all children (ß = -0.17, 95% confidence interval (CI): -0.32, -0.02) and a slower height trajectory in girls (ß = -0.30, 95% CI: -0.52,-0.09; P for interaction = 0.025) and in children born to mothers who smoked during pregnancy (ß = -0.48, 95% CI: -0.83, -1.13; P for interaction = 0.027). We concluded that prenatal cadmium exposure was associated with delayed growth in early childhood. Further research is needed to understand cadmium-related sex differences and the role of coexposure to maternal smoking during early pregnancy.


Asunto(s)
Adiposidad/efectos de los fármacos , Cadmio/efectos adversos , Desarrollo Infantil/efectos de los fármacos , Obesidad Infantil/epidemiología , Efectos Tardíos de la Exposición Prenatal/epidemiología , Presión Sanguínea , Índice de Masa Corporal , Pesos y Medidas Corporales , Cadmio/sangre , Preescolar , Fumar Cigarrillos/epidemiología , Femenino , Desarrollo Fetal/fisiología , Grecia/epidemiología , Humanos , Lactante , Lípidos/sangre , Masculino , Embarazo , Factores Sexuales , Factores Socioeconómicos , Oligoelementos/sangre
3.
Eur J Nutr ; 57(1): 209-218, 2018 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-27655526

RESUMEN

PURPOSE: The study assessed whether diet and adherence to cancer prevention guidelines during pregnancy were associated with micronucleus (MN) frequency in mothers and newborns. MN is biomarkers of early genetic effects that have been associated with cancer risk in adults. METHODS: A total of 188 mothers and 200 newborns from the Rhea cohort (Greece) were included in the study. At early-mid pregnancy, we conducted personal interviews and a validated food frequency questionnaire was completed. With this information, we constructed a score reflecting adherence to the World Cancer Research Fund/American Institute for Cancer Research cancer prevention guidelines on diet, physical activity and body fatness. At delivery, maternal and/or cord blood was collected to measure DNA and hemoglobin adducts of dietary origin and frequencies of MN in binucleated and mononucleated T lymphocytes (MNBN and MNMONO). RESULTS: In mothers, higher levels of red meat consumption were associated with increased MNBN frequency [2nd tertile IRR = 1.34 (1.00, 1.80), 3rd tertile IRR = 1.33 (0.96, 1.85)] and MNMONO frequency [2nd tertile IRR = 1.53 (0.84, 2.77), 3rd tertile IRR = 2.69 (1.44, 5.05)]. The opposite trend was observed for MNBN in newborns [2nd tertile IRR = 0.64 (0.44, 0.94), 3rd tertile IRR = 0.68 (0.46, 1.01)], and no association was observed with MNMONO. Increased MN frequency in pregnant women with high red meat consumption is consistent with previous knowledge. CONCLUSIONS: Our results also suggest exposure to genotoxics during pregnancy might affect differently mothers and newborns. The predictive value of MN as biomarker for childhood cancer, rather than adulthood, remains unclear. With few exceptions, the association between maternal carcinogenic exposures during pregnancy and childhood cancer or early biologic effect biomarkers remains poorly understood.


Asunto(s)
Dieta , Micronúcleos con Defecto Cromosómico/estadística & datos numéricos , Neoplasias/genética , Linfocitos T/ultraestructura , Adulto , Biomarcadores de Tumor/genética , Carcinógenos/administración & dosificación , Exposición a Riesgos Ambientales , Femenino , Sangre Fetal/citología , Grecia , Humanos , Recién Nacido , Masculino , Exposición Materna , Intercambio Materno-Fetal , Madres , Neoplasias/prevención & control , Embarazo , Efectos Tardíos de la Exposición Prenatal , Carne Roja/efectos adversos
4.
BMC Public Health ; 17(1): 836, 2017 10 23.
Artículo en Inglés | MEDLINE | ID: mdl-29061134

RESUMEN

BACKGROUND: The latest scientific reports raise concerns about the rapidly increasing burden of chronic diseases in the state of Qatar. Pregnant Qatari women often confront complications during pregnancy including gestational diabetes, hypertension, abortion and stillbirth. The investigation of early life environmental, genetic, nutritional and social factors that may affect lifelong health is of great importance. Birth cohort studies offer a great opportunity to address early life hazards and their possible long lasting effects on health. METHODS/DESIGN: The Qatari Birth Cohort study is the first mother-child cohort study in the Middle East Area that aims to assess the synergetic role of environmental exposure and genetic factors in the development of chronic disease and monitor woman and child health and/or obstetric characteristics with high prevalence. The present manuscript describes the recruitment phase of the study (duration: 2 years; expected number: 3000 families), where the pregnant Qatari women and their husbands are being contacted before the 15th week of gestation at the Primary Health Care Centers. The consented participants are interviewed to obtain information on several factors (sociodemographic characteristics, dietary habits, occupational/environmental exposure) and maternal characteristics are assessed based on anthropometric measurements, spirometry, and blood pressure. Pregnant women are invited to provide biological samples (blood and urine) in each trimester of their pregnancy, as well as cord blood at delivery. Fathers are also asked to provide biological samples. DISCUSSION: The present study provides invaluable insights into a wide range of early life factors affecting human health. With a geographical focus on the Middle East, it will be a resource for information to the wider scientific community and will allow the formulation of effective policies with a primary focus on public health interventions for maternal and child health.


Asunto(s)
Enfermedad Crónica/epidemiología , Exposición a Riesgos Ambientales/efectos adversos , Interacción Gen-Ambiente , Adolescente , Adulto , Preescolar , Estudios de Cohortes , Femenino , Humanos , Lactante , Recién Nacido , Masculino , Embarazo , Prevalencia , Qatar/epidemiología , Factores de Riesgo , Manejo de Especímenes/métodos , Adulto Joven
5.
Eur J Epidemiol ; 31(11): 1123-1134, 2016 11.
Artículo en Inglés | MEDLINE | ID: mdl-27147065

RESUMEN

The evidence regarding a potential link of low-to-moderate iodine deficiency, selenium status, and cadmium exposure during pregnancy with neurodevelopment is either contradicting or limited. We aimed to assess the prenatal impact of cadmium, selenium, and iodine on children's neurodevelopment at 4 years of age. The study included 575 mother-child pairs from the prospective "Rhea" cohort on Crete, Greece. Exposure to cadmium, selenium and iodine was assessed by concentrations in the mother's urine during pregnancy (median 13 weeks), measured by ICPMS. The McCarthy Scales of Children's Abilities was used to assess children's general cognitive score and seven different sub-scales. In multivariable-adjusted regression analysis, elevated urinary cadmium concentrations (≥0.8 µg/L) were inversely associated with children's general cognitive score [mean change: -6.1 points (95 % CI -12; -0.33) per doubling of urinary cadmium; corresponding to ~0.4 SD]. Stratifying by smoking status (p for interaction 0.014), the association was restricted to smokers. Urinary selenium was positively associated with children's general cognitive score [mean change: 2.2 points (95 % CI -0.38; 4.8) per doubling of urinary selenium; ~0.1 SD], although the association was not statistically significant. Urinary iodine (median 172 µg/L) was not associated with children's general cognitive score. In conclusion, elevated cadmium exposure in pregnancy of smoking women was inversely associated with the children's cognitive function at pre-school age. The results indicate that cadmium may adversely affect neurodevelopment at doses commonly found in smokers, or that there is an interaction with other toxicants in tobacco smoke. Additionally, possible residual confounding cannot be ruled out.


Asunto(s)
Cadmio/orina , Desarrollo Infantil/efectos de los fármacos , Trastornos del Conocimiento/inducido químicamente , Yodo/orina , Efectos Tardíos de la Exposición Prenatal/epidemiología , Selenio/orina , Adulto , Preescolar , Trastornos del Conocimiento/orina , Femenino , Grecia/epidemiología , Humanos , Estudios Longitudinales , Masculino , Madres , Embarazo , Estudios Prospectivos , Adulto Joven
6.
Environ Res ; 146: 379-87, 2016 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-26821262

RESUMEN

BACKGROUND: Bisphenol A (BPA) is a chemical used extensively worldwide in the manufacture of plastic polymers. The environmental obesogen hypothesis suggests that early life exposure to endocrine disrupting chemicals such as BPA may increase the risk for wt gain later in childhood but few prospective epidemiological studies have investigated this relationship. OBJECTIVES: We examined the association of early life BPA exposure with offspring obesity and cardiometabolic risk factors in 500 mother-child pairs from the RHEA pregnancy cohort in Crete, Greece. METHODS: BPA concentrations were measured in spot urine samples collected at the 1st trimester of pregnancy) and from children at 2.5 and 4 years of age. We measured birth wt, body mass index (BMI) from 6 months to 4 years of age, waist circumference, skinfold thickness, blood pressure, serum lipids, C-reactive protein, and adipokines at 4 years of age. BMI growth trajectories from birth to 4 years were estimated by mixed effects models with fractional polynomials of age. Adjusted associations were obtained via multivariable regression analyses. RESULTS: The prevalence of overweight/obesity was 9% at 2, 13% at 3% and 17% at 4 years of age. Geometric mean BPA concentrations were 1.2µg/g creatinine±7.9 in 1st trimester, 5.1µg/g±13.3 in 2.5 years and 1.9µg/g±4.9 in 4 years. After confounder adjustment, each 10-fold increase in BPA at 4 years was associated with a higher BMI z-score (adj. ß=0.2; 95% CI: 0.01, 0.4), waist circumference (adj. ß=1.2; 95% CI: 0.1, 2.2) and sum of skinfold thickness (adj. ß=3.7mm; 95% CI: 0.7, 6.7) at 4 years. Prenatal BPA was negatively associated with BMI and adiposity measures in girls and positively in boys. We found no associations of early life exposure to BPA with other offspring cardiometabolic risk factors. CONCLUSIONS: Prenatal BPA exposure was not consistently associated with offspring growth and adiposity measures but higher early childhood BPA was associated with excess child adiposity.


Asunto(s)
Compuestos de Bencidrilo/orina , Disruptores Endocrinos/orina , Contaminantes Ambientales/orina , Obesidad/epidemiología , Fenoles/orina , Efectos Tardíos de la Exposición Prenatal/epidemiología , Adolescente , Adulto , Antropometría , Análisis Químico de la Sangre , Presión Sanguínea/efectos de los fármacos , Preescolar , Femenino , Grecia/epidemiología , Humanos , Lactante , Masculino , Obesidad/inducido químicamente , Embarazo , Efectos Tardíos de la Exposición Prenatal/inducido químicamente , Estudios Prospectivos , Adulto Joven
7.
Environ Res ; 143(Pt A): 170-6, 2015 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-26496153

RESUMEN

BACKGROUND: Micronuclei (MN) are biomarkers of early genetic effects that have been used to investigate the association between environmental exposures and cancer. However, few studies have examined the association between environmental exposures during pregnancy and MN in mothers and newborns. OBJECTIVES: We examined MN frequency in maternal blood and in cord blood, in relation to maternal air pollution exposure, and the potential interaction with maternal vitamin C intake and maternal smoking. METHODS: We used the cytokinesis-block micronucleus assay to assess MN frequency per 1000 bi-nucleated T-lymphocytes from 181 mothers and 183 newborns born in 2007-2008 in Heraklion (Crete, Greece). The ESCAPE land-use regression methods were used to estimate annual mean exposure to outdoor air pollution [particulate matter (PM), black carbon, nitrogen dioxide (NO2) and nitrogen oxides (NOx)] at maternal home addresses. Food frequency questionnaires were used to estimate maternal dietary vitamin C intake during pregnancy. Smoking habits were self-reported using questionnaires which were checked by measuring maternal urinary cotinine levels. RESULTS: Exposure to PM2.5 was associated with increased MN frequencies in pregnant women [rate ratio [RR (95%CI)] per 5 µg/m(3)=1.53 (1.02, 2.29)]. This increase was considerably higher among women who did not fulfill the recommended vitamin C dietary allowances [RR=9.35 (2.77, 31.61); n=20]. Exposure to PM2.5-10, PM10, NO2 and NOx were also associated with a higher incidence of MN frequencies in smoker women (n=56). No associations were found for newborns. CONCLUSIONS: We found an association between air pollution, particularly PM2.5, and MN frequency in mothers but not in newborns. This association was more pronounced among women with a lower dietary intake of vitamin C during pregnancy and among women who smoked during pregnancy. While results are clear in mothers, the association between maternal carcinogenic exposures during pregnancy and biomarkers of early biologic effect in the newborn remains poorly understood.


Asunto(s)
Contaminantes Atmosféricos/toxicidad , Linfocitos/efectos de los fármacos , Exposición Materna/efectos adversos , Micronúcleos con Defecto Cromosómico/inducido químicamente , Material Particulado/toxicidad , Efectos Tardíos de la Exposición Prenatal/inducido químicamente , Adulto , Ácido Ascórbico/administración & dosificación , Ácido Ascórbico/uso terapéutico , Estudios de Cohortes , Femenino , Sangre Fetal/citología , Grecia/epidemiología , Humanos , Recién Nacido , Linfocitos/patología , Masculino , Exposición Materna/prevención & control , Micronúcleos con Defecto Cromosómico/efectos de los fármacos , Micronúcleos con Defecto Cromosómico/estadística & datos numéricos , Tamaño de la Partícula , Embarazo , Efectos Tardíos de la Exposición Prenatal/epidemiología , Efectos Tardíos de la Exposición Prenatal/genética , Efectos Tardíos de la Exposición Prenatal/prevención & control , Fumar/efectos adversos , Fumar/epidemiología , Encuestas y Cuestionarios
8.
BMC Med ; 12: 110, 2014 Jul 11.
Artículo en Inglés | MEDLINE | ID: mdl-25012562

RESUMEN

BACKGROUND: Preterm birth (PB) and fetal growth restriction (FGR) convey the highest risk of perinatal mortality and morbidity, as well as increasing the chance of developing chronic disease in later life. Identifying early in pregnancy the unfavourable maternal conditions that can predict poor birth outcomes could help their prevention and management. Here we used an exploratory metabolic profiling approach (metabolomics) to investigate the association between birth outcomes and metabolites in maternal urine collected early in pregnancy as part of the prospective mother-child cohort Rhea study. Metabolomic techniques can simultaneously capture information about genotype and its interaction with the accumulated exposures experienced by an individual from their diet, environment, physical activity or disease (the exposome). As metabolic syndrome has previously been shown to be associated with PB in this cohort, we sought to gain further insight into PB-linked metabolic phenotypes and to define new predictive biomarkers. METHODS: Our study was a case-control study nested within the Rhea cohort. Major metabolites (n = 34) in maternal urine samples collected at the end of the first trimester (n = 438) were measured using proton nuclear magnetic resonance spectroscopy. In addition to PB, we used FGR in weight and small for gestational age as study endpoints. RESULTS: We observed significant associations between FGR and decreased urinary acetate (interquartile odds ratio (IOR) = 0.18 CI 0.04 to 0.60), formate (IOR = 0.24 CI 0.07 to 0.71), tyrosine (IOR = 0.27 CI 0.08 to 0.81) and trimethylamine (IOR = 0.14 CI 0.04 to 0.40) adjusting for maternal education, maternal age, parity, and smoking during pregnancy. These metabolites were inversely correlated with blood insulin. Women with clinically induced PB (IPB) had a significant increase in a glycoprotein N-acetyl resonance (IOR = 5.84 CI 1.44 to 39.50). This resonance was positively correlated with body mass index, and stratified analysis confirmed that N-acetyl glycoprotein and IPB were significantly associated in overweight and obese women only. Spontaneous PB cases were associated with elevated urinary lysine (IOR = 2.79 CI 1.20 to 6.98) and lower formate levels (IOR = 0.42 CI 0.19 to 0.94). CONCLUSIONS: Urinary metabolites measured at the end of the first trimester are associated with increased risk of negative birth outcomes, and provide novel information about the possible mechanisms leading to adverse pregnancies in the Rhea cohort. This study emphasizes the potential of metabolic profiling of urine as a means to identify novel non-invasive biomarkers of PB and FGR risk.


Asunto(s)
Retardo del Crecimiento Fetal/orina , Primer Trimestre del Embarazo/orina , Nacimiento Prematuro/orina , Adulto , Biomarcadores/orina , Índice de Masa Corporal , Peso Corporal , Estudios de Casos y Controles , Niño , Estudios de Cohortes , Femenino , Grecia , Humanos , Recién Nacido , Síndrome Metabólico/orina , Metaboloma , Obesidad/orina , Oportunidad Relativa , Sobrepeso/orina , Embarazo , Estudios Prospectivos , Riesgo
9.
Epidemiology ; 25(2): 215-24, 2014 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-24487205

RESUMEN

BACKGROUND: Maternal exposure to dioxins and dioxin-like compounds may affect fetal growth and development. We evaluated the association between in utero dioxin-like activity and birth outcomes in a prospective European mother-child study. METHODS: We measured dioxin-like activity in maternal and cord blood plasma samples collected at delivery using the Dioxin-Responsive Chemically Activated LUciferase eXpression (DR CALUX) bioassay in 967 mother-child pairs, in Denmark, Greece, Norway, Spain, and England. Multiple linear regression models were used to investigate the associations with birth weight, gestational age, and head circumference. RESULTS: Plasma dioxin-like activity was higher in maternal sample than in cord samples. Birth weight was lower with medium (-58 g [95% confidence interval (CI) = -176 to 62]) and high (-82 g [-216 to 53]) tertiles of exposure (cord blood) compared with the lowest tertile. Gestational age was shorter by approximately half a week in the highest compared with the lowest (-0.4 weeks [95% CI = -0.8 to -0.1]). This association was stronger in boys than in girls, although the statistical evidence for interaction was weak (P = 0.22). Analysis based on CALUX-toxic equivalents expressed per milliliter of plasma showed similar trends. We found no association between dioxin-like activity in maternal plasma and birth outcomes. CONCLUSIONS: Results from this international general population study suggest an association between low-level prenatal dioxin-like activity and shorter gestational age, particularly in boys, with weaker associations for birth weight.


Asunto(s)
Peso al Nacer/efectos de los fármacos , Dioxinas/toxicidad , Contaminantes Ambientales/toxicidad , Exposición Materna/efectos adversos , Nacimiento Prematuro/inducido químicamente , Adulto , Bioensayo , Dioxinas/sangre , Contaminantes Ambientales/sangre , Europa (Continente) , Femenino , Sangre Fetal/química , Edad Gestacional , Humanos , Recién Nacido , Modelos Lineales , Masculino , Embarazo , Estudios Prospectivos , Factores Sexuales
10.
Mutagenesis ; 29(6): 393-400, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25296962

RESUMEN

The use of biomarkers of early genetic effects, predictive for cancer, such as micronuclei (MN) in lymphocytes, may help to investigate the association between diet and cancer. We hypothesised that the presence of mutagens in the diet may increase MN formation. A 'pooled' standardised analysis was performed by applying the same experimental protocol for the cytokinesis block micronucleus assay in 625 young healthy women after delivery from five European study populations (Greece, Denmark, UK, Spain and Norway). We assessed MN frequencies in mono- and binucleated T-lymphocytes (MNMONO and MNBN) and the cytokinesis blocked proliferation index using a semi-automated image analysis system. Food frequency questionnaires (FFQs) were used to estimate intake of fatty acids and a broad range of immunotoxic and genotoxic/carcinogenic compounds through the diet. Pooled difference based on delivery type revealed higher MNMONO frequencies in caesarean than in vaginal delivery (P = 0.002). Statistical analysis showed a decrease in MNMONO frequencies with increasing calculated omega-6 PUFA concentrations and a decrease in MNBN frequencies with increasing calculated omega-3 PUFA concentrations. The expected toxic compounds estimated by FFQs were not associated with MN formation in mothers after delivery. In pregnant women, an omega-3 and -6 rich diet estimated by FFQ is associated with lower MN formation during pregnancy and delivery.


Asunto(s)
Dieta , Conducta Alimentaria , Micronúcleos con Defecto Cromosómico , Encuestas y Cuestionarios , Población Blanca , Adulto , Proliferación Celular/efectos de los fármacos , Estudios de Cohortes , Citocinesis/efectos de los fármacos , Femenino , Humanos , Modelos Lineales , Persona de Mediana Edad , Mutágenos/toxicidad , Embarazo , Linfocitos T/metabolismo
11.
Psychoneuroendocrinology ; 166: 107060, 2024 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-38677195

RESUMEN

BACKGROUND: The placenta acts as a buffer to regulate the degree of fetal exposure to maternal cortisol through the 11-Beta Hydroxysteroid Dehydrogenase isoenzyme type 2 (11-ß HSD2) enzyme. We conducted a systematic review and meta-analysis to assess the effect of prenatal psychological distress (PPD) on placental 11-ß HSD2 gene expression and explore the related mechanistic pathways involved in fetal neurodevelopment. METHODS: We searched PubMed, Embase, Scopus, APA PsycInfo®, and ProQuest Dissertations for observational studies assessing the association between PPD and 11-ß HSD2 expression in human placentas. Adjusted regression coefficients (ß) and corresponding 95% confidence intervals (CIs) were pooled based on three contextual PPD exposure groups: prenatal depression, anxiety symptoms, and perceived stress. RESULTS: Of 3159 retrieved records, sixteen longitudinal studies involving 1869 participants across seven countries were included. Overall, exposure to PPD disorders showed weak negative associations with the placental 11-ß HSD2 gene expression as follows: prenatal depression (ß -0.01, 95% CI 0.05-0.02, I2=0%), anxiety symptoms (ß -0.02, 95% CI 0.06-0.01, I2=0%), and perceived stress (ß -0.01 95% CI 0.06-0.04, I2=62.8%). Third-trimester PPD exposure was more frequently associated with lower placental 11-ß HSD2 levels. PPD and placental 11-ß HSD2 were associated with changes in cortisol reactivity and the development of adverse health outcomes in mothers and children. Female-offspring were more vulnerable to PPD exposures. CONCLUSION: The study presents evidence of a modest role of prenatal psychological distress in regulating placental 11-ß HSD2 gene expression. Future prospective cohorts utilizing larger sample sizes or advanced statistical methods to enhance the detection of small effect sizes should be planned. Additionally, controlling for key predictors such as the mother's ethnicity, trimester of PPD exposure, mode of delivery, and infant sex is crucial for valid exploration of PPD effects on fetal programming.


Asunto(s)
11-beta-Hidroxiesteroide Deshidrogenasa de Tipo 2 , Placenta , Complicaciones del Embarazo , Distrés Psicológico , Estrés Psicológico , Humanos , Embarazo , 11-beta-Hidroxiesteroide Deshidrogenasa de Tipo 2/genética , 11-beta-Hidroxiesteroide Deshidrogenasa de Tipo 2/metabolismo , Femenino , Placenta/metabolismo , Estrés Psicológico/metabolismo , Estrés Psicológico/genética , Complicaciones del Embarazo/genética , Complicaciones del Embarazo/metabolismo , Complicaciones del Embarazo/psicología , Depresión/genética , Depresión/metabolismo , Expresión Génica/genética , Ansiedad/genética , Ansiedad/metabolismo , Hidrocortisona/metabolismo , Efectos Tardíos de la Exposición Prenatal/genética , Efectos Tardíos de la Exposición Prenatal/metabolismo
12.
FASEB J ; 26(10): 3946-56, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-22730438

RESUMEN

The relevance of preconceptional and prenatal toxicant exposures for genomic stability in offspring is difficult to analyze in human populations, because gestational exposures usually cannot be separated from preconceptional exposures. To analyze the roles of exposures during gestation and conception on genomic stability in the offspring, stability was assessed via the Comet assay and highly sensitive, semiautomated confocal laser scans of γH2AX foci in cord, maternal, and paternal blood as well as spermatozoa from 39 families in Crete, Greece, and the United Kingdom. With use of multivariate linear regression analysis with backward selection, preconceptional paternal smoking (% tail DNA: P>0.032; γH2AX foci: P>0.018) and gestational maternal (% tail DNA: P>0.033) smoking were found to statistically significantly predict DNA damage in the cord blood of F1 offspring. Maternal passive smoke exposure was not identified as a predictor of DNA damage in cord blood, indicating that the effect of paternal smoking may be transmitted via the spermatozoal genome. Taken together, these studies reveal a role for cigarette smoke in the induction of DNA alterations in human F1 offspring via exposures of the fetus in utero or the paternal germline. Moreover, the identification of transgenerational DNA alterations in the unexposed F1 offspring of smoking-exposed fathers supports the claim that cigarette smoke is a human germ cell mutagen.


Asunto(s)
Sangre Fetal/metabolismo , Inestabilidad Genómica/efectos de los fármacos , Inestabilidad Genómica/genética , Exposición Materna/efectos adversos , Fumar/efectos adversos , Adolescente , Adulto , Ensayo Cometa , Cotinina/orina , Daño del ADN/efectos de los fármacos , Daño del ADN/genética , Femenino , Humanos , Recién Nacido , Masculino , Análisis Multivariante , Embarazo , Adulto Joven
13.
Paediatr Perinat Epidemiol ; 27(5): 461-71, 2013 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-23930782

RESUMEN

BACKGROUND: Leptin is an adipocyte-secreted hormone that regulates energy homeostasis, while its role in fetal programming remains poorly understood. We aimed to evaluate the effect of maternal weight status on cord blood leptin levels and their combined effect on fetal growth. METHODS: We included 638 mother-child pairs from the prospective mother-child cohort 'Rhea' study in Crete, Greece with singleton pregnancies, providing cord blood serum samples for leptin analysis and complete data on birth outcomes. Multivariable logistic and linear regression models were used adjusting for confounders. Generalised additive models were used to explore the form of the relationship between cord leptin and continuous birth outcomes. RESULTS: Log cord leptin was positively associated with birthweight {ß-coef: 176.5 [95% confidence interval (CI): 133.0, 220.0] }, ponderal index (ß-coef: 1.0 [95% CI: 0.6, 1.4] ) and gestational age (ß-coef: 0.7 [95% CI: 0.5, 0.8] ). Excessive weight gain during pregnancy was associated with a threefold increased risk for cord hyperleptinaemia {relative risk (RR): 3.0, [95% CI: 1.5, 6.3] }. Maternal pre-pregnancy overweight/obesity [body mass index (BMI) ≥25 kg/m(2) ] increased the risk of giving birth to a hyperleptinaemic neonate (RR: 2.1 [95% CI: 1.4, 3.2] and the effect of log leptin on birthweight (ß-coef: 219.1 [95% CI: 152.3, 285.9] compared with women with a BMI <25 kg/m(2) (ß-coef: 150.5 [95% CI: 93.1, 207.9]. CONCLUSIONS: Higher cord blood leptin levels are associated with increased size at birth and gestational age, while maternal pre-pregnancy BMI and weight gain during pregnancy represent significant indicators of cord blood leptin.


Asunto(s)
Peso Corporal/fisiología , Sangre Fetal/metabolismo , Desarrollo Fetal/fisiología , Leptina/sangre , Aumento de Peso/fisiología , Adulto , Índice de Masa Corporal , Estudios de Cohortes , Femenino , Edad Gestacional , Grecia , Humanos , Madres , Embarazo , Estudios Prospectivos , Análisis de Regresión
14.
Tob Control ; 22(3): 194-200, 2013 May.
Artículo en Inglés | MEDLINE | ID: mdl-22253001

RESUMEN

BACKGROUND: To date, no research exists on the role that different sources of exposure to second-hand smoke (SHS) have on 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and nicotine uptake, assessed via urinary 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) and cotinine concentrations of non-smoking pregnant women, nor the differences in NNAL concentrations among pregnant women who quit smoking in comparison to those who do not. METHODS: As part of the 'Rhea' mother childbirth cohort in Crete, Greece, 1317 mother-child pairs were followed-up until delivery, while among a subsample, maternal urine was assessed for its NNAL (n=117) and cotinine concentrations (n=377). RESULTS: Pregnant women who continued to smoke during pregnancy were found to have geometric mean urinary NNAL concentrations of 0.612 pmol/ml, in comparison to the 0.100 pmol/ml of ex-smokers and 0.0795 pmol/ml of non-smokers exposed to SHS. Exposure to SHS in the home was associated with a 4.40 ng/ml increase in urinary cotinine levels, while reported exposure to SHS in cars was associated with an even higher (8.73 ng/ml) increase in cotinine concentrations and was strongly related to NNAL concentrations. Exposure to SHS in the workplace and in public places was also shown to increase cotinine and NNAL concentrations. The NNAL:cotinine ratio was found to be higher among pregnant women who were exposed to SHS but did not smoke (p<0.001). CONCLUSIONS: Using cotinine levels as an indicator of NNK, exposure due to SHS during pregnancy leads to an underestimation of exposure to NNK uptake. Moreover, each source of exposure contributed to the increase in cotinine levels, indicating the importance of avoiding SHS exposure from any source.


Asunto(s)
Cotinina/orina , Nitrosaminas/orina , Embarazo/orina , Piridinas/orina , Contaminación por Humo de Tabaco/análisis , Contaminación del Aire Interior/análisis , Biomarcadores/orina , Exposición a Riesgos Ambientales/análisis , Monitoreo del Ambiente/métodos , Femenino , Estudios de Seguimiento , Humanos , Autoinforme , Fumar/orina , Cese del Hábito de Fumar , Manejo de Especímenes/métodos , Esposos/estadística & datos numéricos
15.
Eur J Pediatr ; 171(10): 1563-6, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-22855221

RESUMEN

Cord leptin is a biomarker of fetal growth and adiposity with a role in predicting weight gain during the first months of life and childhood obesity. Our objective was to calculate gender-specific reference intervals for cord blood leptin in healthy neonates in Crete, Greece. We used data from the prospective mother-child cohort ("Rhea" study) in Crete, Greece. The analysis included 398 neonates chosen with strict inclusion criteria based on maternal and fetal characteristics. Cord leptin reference intervals for male neonates were 1.4-18.2 ng/mL and for females 2.0-25.8 ng/mL. Females had higher leptin levels (median 7.4; IQR 4.7-10.9) compared to males (median 4.9; IQR 3.2-7.6) (p < 0.001). Conclusion Gender-specific reference ranges are essential in clinical practice for correct interpretation of leptin values in cord blood and early detection of childhood obesity.


Asunto(s)
Sangre Fetal/química , Recién Nacido/sangre , Leptina/sangre , Biomarcadores/sangre , Estudios de Cohortes , Ensayo de Inmunoadsorción Enzimática , Femenino , Grecia , Humanos , Masculino , Estudios Prospectivos , Valores de Referencia , Factores Sexuales
16.
Acta Biomed ; 93(1): e2022033, 2022 03 14.
Artículo en Inglés | MEDLINE | ID: mdl-35315407

RESUMEN

BACKGROUND AND AIM OF THE WORK: Qatar Biobank (QBB) is actively acquiring data on the range of short- and long-term health impacts associated with COVID-19. This is performed through the COVID-19 biorepository National project. In this report, we describe the most common indications for the referral to Qatar's healthcare system of COVID-19 biorepository participants in comparison with the Qatar Biobank (QBB) general population study. Methods Patients with a laboratory diagnosis of COVID-19, who were Qatar residents that could communicate in Arabic, English, Hindi and Urdu were eligible to participate in the COVID-19 biorepository project. Biological samples of Consented participants were collected on a weekly basis until recovery, and then monthly for a year. Participants were also offered a bone density scan three months after recovery and non-contrast MRI brain and whole-body scan six months after recovery. Number of participants requiring referral for medical follow up after recovery for any abnormal clinically significant findings were recorded and statistically compared to general population referred participants Results: The majority of referrals for the general population study was for osteopenia versus diabetes for the COVID-19 biorepository project Conclusion Descriptive analysis of the referral data of the COVID-19 participants and QBB general population (not previously affected by the virus) shows a clear difference between the two populations' reasons for referrals. Diabetes for COVID 19 recovered participants versus osteopenia for general population Keywords: COVID19, Reason for Referrals, Diabetes, Qatar biobank.


Asunto(s)
COVID-19 , Bancos de Muestras Biológicas , Atención a la Salud , Humanos , Qatar/epidemiología , Derivación y Consulta
17.
Xenobiotica ; 41(6): 456-63, 2011 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-21381896

RESUMEN

Exposure to toxic metals during pregnancy may have detrimental effects on foetal development. We assessed the role of sociodemographic characteristics and active and passive smoking on blood concentrations of metals (As, Cd, Pb, Hg, Sb, U, Mn and Mo). Venous blood drawn from 50 pregnant women, randomly selected from the mother-child birth cohort 'Rhea'. Extensive questionnaire data on active and passive smoking were collected. Urinary cotinine was measured to validate self-reported exposure and non-smoking status. Smokers had higher concentrations of Cd (1.0 µg/L) as compared with non-smokers (0.29 µg/L, P < 0.001) and a tendency for higher As and Hg. Among non-smokers, blood As and Hg concentrations were also associated with exposure to passive smoking in public venues and the family home and to overall greater secondhand smoke (SHS) exposure (As: 0.97µg/L among heavy-exposed compared with 0.20 µg/L among the low-exposed, P < 0.05; Hg: 2.1 µg/L vs. 0.9 µg/L respectively, P < 0.05). Controlling for fish and seafood intake altered the statistical significance but not the direction of the above associations. Smoking was associated with higher Cd concentrations in pregnant women, although the association between passive smoking and elevated As and Hg concentrations was indicative, however inconclusive.


Asunto(s)
Sustancias Peligrosas/sangre , Metales/sangre , Fumar/epidemiología , Contaminación por Humo de Tabaco/estadística & datos numéricos , Adulto , Estudios de Cohortes , Cotinina/orina , Demografía , Femenino , Grecia/epidemiología , Humanos , Exposición Materna/estadística & datos numéricos , Embarazo , Fumar/sangre , Fumar/orina , Encuestas y Cuestionarios
18.
In Vivo ; 23(1): 69-76, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19368127

RESUMEN

Fibrosarcoma is an uncommon soft tissue tumor with a complex cell microenvironment, particularly rich in glycosaminoglycans/proteoglycans (GAGs/PGs). Chondroitin sulfate proteoglycans (CSPGs) participate in the modulation of various cellular functions, including adhesion and migration. The role of chondroitin sulfate (CS) chains on adhesion, chemotaxis and migration of poorly differentiated fibrosarcoma B6FS cell was studied, utilizing exogenous CS treatment and chondroitinase digestions as well as specific modulators of CS synthesis. Cleavage of cell-associated CS chains and specific inhibition of endogenous CS production severely impaired these fibrosarcoma cell functions. These results show that the reduction of endogenous CSPG expression as well as cleavage of the CS chain inhibited fibrosarcoma cell motility, migration and adhesion. Treatment with free CS chains enhanced cell chemotaxis and migration, whereas adhesion was inhibited. CS chains were found to upregulate cell motility through the MAPK pathway, specifically through JNK, whereas CS-induced migration was found to require tyrosine kinase dependent pathways. This study suggests a new role of CS on tumor cell adhesion, chemotaxis and migration.


Asunto(s)
Antineoplásicos/farmacología , Movimiento Celular/efectos de los fármacos , Sulfatos de Condroitina/farmacología , Fibrosarcoma/tratamiento farmacológico , MAP Quinasa Quinasa 4/metabolismo , Proteínas Tirosina Quinasas/metabolismo , Adhesión Celular/efectos de los fármacos , Línea Celular Tumoral , Quimiotaxis/efectos de los fármacos , Fibrosarcoma/enzimología , Fibrosarcoma/fisiopatología , Humanos , Transducción de Señal/efectos de los fármacos , Cicatrización de Heridas
19.
Biopreserv Biobank ; 17(6): 491-493, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31833811

RESUMEN

Biobank science is progressively becoming indispensable for the development of novel diagnostic tools in health care, by pairing standardized high-quality biological samples, phenotypic, and omics data required to best characterize the underlying biological mechanisms of response to therapy and survival. Qatar Biobank (QBB), Qatar's National Repository Centre for biological samples and health information, aligning with these endeavors, has developed a strategic framework to enable biobanking science that can be transformed into tangible health care diagnostic tools. In this concept, QBB works closely with multidisciplinary stakeholders: (1) governmental authorities (n = 2), (2) health providers (n = 3), (3) academic institutions (n = 28), (4) other research institutions (n = 6), and (5) the Qatar National Research Fund, by providing data and biospecimens to research projects. The local community organizes campaigns through social media and interactive events, spreading the concept of biobanking to inform and encourage people to participate. Up to now, QBB has recruited up to 30% of the targeted population and collaborated with 35 national and international research entities contributing to more than 170 research projects. QBB is referring about 53% of its participants to the Hamad general hospital through the integrated information system, revealing the need of new health screening approaches for public health policy makers. QBB contributed to the development of a customized genetic screening microarray tailored to the Qatari population that will be used in research as well as for the screening of variants of medical relevance in Qatar, promoting precision medicine in Qatar's health care system. The QBB strategic plan is a paradigm for the optimal utilization of resources, infrastructure, and investments engaging the local authorities and the research entities, and committing them to data sharing and working together toward the discovery of evidence-based health care interventions.


Asunto(s)
Bancos de Muestras Biológicas , Práctica Clínica Basada en la Evidencia/métodos , Humanos , Difusión de la Información , Cooperación Internacional , Medicina de Precisión , Qatar , Investigación Biomédica Traslacional
20.
Biopreserv Biobank ; 17(6): 494-505, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31833809

RESUMEN

The overall goal of the Qatar Biobank (QBB) is to collect, manage, and distribute high-quality human biospecimens with appropriate clinical and/or research annotation and associated phenotypic data, aiming to be an important and essential resource of medical research and evidence-based health care system policies in Qatar. To manage and collect large volumes of data, the QBB has been investing in a number of information management solutions, trying to avoid inflexibility of traditional systems and accommodate changes in data sources and workflows. This article aims to present the information technology solutions of QBB based on a free, open-source software solution, considered a reliable alternative to commercial solutions. After evaluating the free, open-source software solutions available for biobanks, Onyx from ObiBa was utilized to develop custom components to interface various clinical devices, LIMS and Picture Archiving and Communication System, which has varying integration capabilities. This is a showcase for biobanks to carefully evaluate and select hardware and software to automate their operations providing the functions required for business continuity.


Asunto(s)
Bancos de Muestras Biológicas/organización & administración , Bancos de Muestras Biológicas/normas , Atención a la Salud , Práctica Clínica Basada en la Evidencia , Humanos , Gestión de la Información , Tecnología de la Información , Qatar , Programas Informáticos
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