11 research outputs found

    Study of factors related to childhood leukemia and to central nervous system tumors in California

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    Childhood leukemia is the most common malignant disease in children, followed by childhood CNS/brain tumors. [1, 2] Both diseases have been recognized for a long time but little is known about the etiology of childhood leukemia and primary CNS/brain tumors. The aims of this project were to evaluate: 1) the association of several perinatal factors with childhood leukemia as well as with CNS/brain tumors; 2) the relationships between childhood leukemia and child's and parental race, Hispanic ethnicity and socio-economic status (SES) at individual and census levels; 3) factors associated with residential mobility in childhood leukemia cases. We conducted a large registry-based study in California using California birth and cancer registries to obtain information on childhood leukemia and CNS/brain tumor cases and controls. Information on case's diagnosis, histological subtypes, age at diagnosis, sex, and diagnosis address was obtained from California cancer registry; information on perinatal factors (birth weight, gestational age, birth order, parental age at birth, maternal complications during pregnancy, abnormal condition of a newborn), socio-demographic factors (date of birth, sex, race and ethnicity of parents and child, parental education, sources of payment for delivery, birth address) were obtained from the birth registry. We linked California cancer and birth registries to obtain information on 5788 cases of childhood leukemia and 3308 cases of CNS/brain tumors and their 5788 and 3308 controls matched on age and sex (1:1). To address at least partially the problem with misclassification we categorized birth weight, gestational age, parental age, child and parental race and Hispanic ethnicity, individual level proxies for and census-based SES in several ways. For all analyses we used conditional logistic regression, with adjustment for potential confounders. Our results for childhood leukemia and perinatal factors indicate that high birth weight and LGA were associated with increased risk and SGA with decreased risk of total childhood leukemia and ALL, being first-born was associated with decreased risk of AML, and advanced paternal age was associated with increased risk of ALL. Our results for CNS/brain tumors and perinatal factors suggest that maternal genital herpes, blood and immunological disorders during pregnancy and newborn CNS abnormalities were associated with increased risk of CNS tumors. Maternal infections during pregnancy were associated with decreased risk of CNS tumors. Factors associated with childhood leukemia and CNS tumors varied by subtype, an indicator of different etiology for different subtypes. We noted that Black children had decreased risk (ref. - White) and Hispanic children (ref. non-Hispanic) had increased risk of total childhood leukemia and ALL. Asian race was associated with increased risk of AML. These differences in the incidence of childhood leukemia indicate that some genetic and/or environmental/cultural (e.g., diet or lifestyle) factors are involved in etiology of childhood leukemia. We found no evidence to support the suggestion that SES, as measured by variety of proxies is a determinant of childhood leukemia and of its both subtypes. It is likely that results of many previous studies that found an association between childhood leukemia and SES were largely influenced by selection or ecological bias. The results of this study indicate that childhood leukemia cases in California are residentially very mobile, with 58% of them moving between birth and diagnosis. The residential mobility of childhood leukemia cases notably varied by time interval between birth and diagnosis, child's race/ethnicity, maternal age at birth, census-based SES, and the source of payment for delivery; it varied less by the distance to the nearest power line. Our results suggest that even if information on the residential mobility of subjects is unavailable, it might be possible and important to look at the distribution of factors that could be associated with residential mobility

    Epidemiologic study of residential proximity to transmission lines and childhood cancer in California: description of design, epidemiologic methods and study population.

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    We conducted a large epidemiologic case-control study in California to examine the association between childhood cancer risk and distance from the home address at birth to the nearest high-voltage overhead transmission line as a replication of the study of Draper et al. in the United Kingdom. We present a detailed description of the study design, methods of case ascertainment, control selection, exposure assessment and data analysis plan. A total of 5788 childhood leukemia cases and 3308 childhood central nervous system cancer cases (included for comparison) and matched controls were available for analysis. Birth and diagnosis addresses of cases and birth addresses of controls were geocoded. Distance from the home to nearby overhead transmission lines was ascertained on the basis of the electric power companies' geographic information system (GIS) databases, additional Google Earth aerial evaluation and site visits to selected residences. We evaluated distances to power lines up to 2000 m and included consideration of lower voltages (60-69 kV). Distance measures based on GIS and Google Earth evaluation showed close agreement (Pearson correlation >0.99). Our three-tiered approach to exposure assessment allowed us to achieve high specificity, which is crucial for studies of rare diseases with low exposure prevalence

    Childhood leukaemia and distance from power lines in California: a population-based case-control study

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    BACKGROUND: Studies have reported an increased risk of childhood leukaemia associated with living near high-voltage electric power transmission lines that extend to distances at which magnetic fields from lines are negligible. We conducted a large records-based case-control study of childhood leukaemia risk in the population living near power lines in California. METHODS: The study included 5788 childhood leukaemia and 3308 central nervous system (CNS) cancer cases (for comparison) born in and diagnosed in California (1986–2008), and matched to population-based controls by age and sex. We geocoded birth address and estimated the distance from residence to transmission lines using geographic information systems, aerial imagery, and, for some residences, site visits. RESULTS: For leukaemia, there was a slight excess of cases within 50 m of a transmission line over 200 kV (odds ratio 1.4, 95% confidence interval 0.7–2.7). There was no evidence of increased risk for distances beyond 50 m, for lower-voltage lines, or for CNS cancers. CONCLUSIONS: Our findings did not clearly support an increased childhood leukaemia risk associated with close proximity (<50 m) to higher voltage lines, but could be consistent with a small increased risk. Reports of increased risk for distances beyond 50 m were not replicated

    Trajectories of Viral Suppression in People Living With HIV Receiving Coordinated Care: Differences by Comorbidities.

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    BackgroundIn March of 2013, the Los Angeles County (LAC) Division of HIV and STD Programs implemented a clinic-based Medical Care Coordination (MCC) Program to increase viral suppression (VS) (&lt;200 c/mL) among people living with HIV (PLWH) at high risk for poor health outcomes.ObjectiveThis study aimed to estimate trajectories of VS and to assess whether these trajectories differed by stimulant use, housing instability, and depressive symptom severity as reported by PLWH participating in MCC.MethodsData represent 6408 PLWH in LAC receiving services from the MCC Program and were obtained from LAC HIV surveillance data matched to behavioral assessments obtained across 35 Ryan White Program clinics participating in MCC. Piecewise mixed-effects logistic regression with a random intercept estimated probabilities of VS from 12 months before MCC enrollment through 36 months after enrollment, accounting for time by covariate interactions for 3 comorbid conditions: housing instability, stimulant use, and depressive symptoms.ResultsThe overall probability of VS increased from 0.35 to 0.77 within the first 6 months in the MCC Program, and this probability was maintained up to 36 months after enrollment. Those who reported housing instability, stimulant use, or multiple comorbid conditions did not achieve the same probability of VS by 36 months as those with none of those comorbidities.ConclusionsFindings suggest that MCC improved the probability of VS for all patient groups regardless of the presence of comorbidities. However, those with comorbid conditions will still require increased support from patient-centered programs to address disparities in VS
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