The CHAMA-COS (Center for the Health Assessment of Mothers and Children of Salinas) project, a component of the Center for Children’s Environmental Health Research at the University of California, Berkeley, is a longitudinal birth cohort study of the effects of pesticides and other environmental exposures on the health of pregnant women and their children living in the Salinas Valley. Pregnant women entering prenatal care at Natividad Medical Center, a county hospital located in the town of Salinas, or at one of five centers of Clinica de Salud del Valle de Salinas (located in Castroville, Salinas, Soledad, and Greenfield) were screened for eligibility over 1 year between October 1999 and October 2000. Clinica de Salud del Valle de Salinas is a network of community clinics located throughout the Salinas Valley and serving a low-income population, many of whom are farm workers.
Eligible women were ≥ 18 years of age, < 20 weeks gestation at enrollment, English or Spanish speaking, Medi-Cal eligible, and planning to deliver at the Natividad Medical Center. Of 1,130 eligible women, 601 (53.2%) agreed to participate in this multiyear study. Women who declined to participate were similar to study subjects in age and parity but were more likely to be English speaking and born in the United States and less likely to be living with agricultural field workers. After losses due to miscarriage, moving, or dropping from the study before delivery, birth weight information was available for 538 women. We excluded from these analyses women with gestational or preexisting diabetes (n = 26), hypertension (n = 15), twin births (n = 5), or stillbirths (n = 3). We also excluded one woman for whom birth weight information was out of range (< 500 g). Eleven infants diagnosed with congenital anomalies at birth [International Classification of Diseases, 9th Revision (ICD-9; 1989 ) codes 740–759] were included in the final sample because their exclusion did not materially affect the results. The final sample size was 488. Written informed consent was obtained from all participants, and the study was approved by the institutional review boards.