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Berens, Anne E.

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Berens

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Anne E.

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Berens, Anne E.

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  • Publication

    Measuring Psychosocial Adversity as a Neurodevelopmental Risk Factor: Development & Validation of the Childhood Psychosocial Adversity Questionnaire–Bangladesh (CPAQ-B)

    (2018-05-15) Berens, Anne E.

    BACKGROUND: Research examining effects of psychosocial adversities on child neurocognitive development has occurred largely in high-income countries. A key barrier to global extension of this work has been a lack of culturally appropriate measurement tools. This thesis reports on the development, validation, and initial application of the Childhood Psychosocial Adversity Questionnaire–Bangladesh (CPAQ-B), the first context-tailored tool to assess early childhood psychosocial adversity comprehensively as a neurodevelopmental risk factor in a low-resource setting. PARTICIPANTS: 355 mother-child dyads from an urban slum of Dhaka, Bangladesh took part in qualitative work (N=45), item pretesting (N=25), questionnaire piloting (N=53), and administration of the CPAQ-B (N=232) at child ages 18, 24, 48, and/or 60 months. Community-based clinicians (N=35) also participated in qualitative sessions. METHODS: A conceptual model of early psychosocial adversity was developed to inform item selection. Initial items underwent expert review, pretesting, piloting, and item reduction. The CPAQ-B was then administered for psychometric analysis and validation including assessment of internal consistency, test-retest and inter-rater reliability, and criterion and predictive validity via correlation with parallel measures and child IQ scores. Finally, as an initial use of the tool, multivariate ordinary least squares regression modeling was used to assess whether 48-month CPAQ-B scores predict 60-month child intelligent quotient (IQ) scores when controlling for concurrent risks. RESULTS: 180 initial items were generated and piloted, and reduced to 64 items in the final scale. Exploratory factor analysis supported 11 subscales assessing for child maltreatment, various maternal and family stressors, and neighborhood-level exposures. Evidence supported strong subscale internal consistency and full-scale test-retest and inter-rater reliability. Subscale and full-scale scores correlated significantly with comparator measures. 48-month CPAQ-B scores significantly predicted 60-month WPPSI-IV IQ in multivariate regression models controlling for socioeconomic variables and malnutrition. CONCLUSIONS: The CPAQ-B represents a novel research tool measuring childhood psychosocial adversities, with good initial validity evidence for use among low-SES children ages 18-60 months in Dhaka, Bangladesh. Future work may adapt the instrument for use in other countries in the region, while methods may inform similar efforts to develop context-tailored assessments across other socio-cultural settings.

  • Publication

    Biological embedding of childhood adversity: from physiological mechanisms to clinical implications

    (BioMed Central, 2017) Berens, Anne E.; Jensen, Sarah; Nelson, Charles

    Background: Adverse psychosocial exposures in early life, namely experiences such as child maltreatment, caregiver stress or depression, and domestic or community violence, have been associated in epidemiological studies with increased lifetime risk of adverse outcomes, including diabetes, heart disease, cancers, and psychiatric illnesses. Additional work has shed light on the potential molecular mechanisms by which early adversity becomes “biologically embedded” in altered physiology across body systems. This review surveys evidence on such mechanisms and calls on researchers, clinicians, policymakers, and other practitioners to act upon evidence. Observations Childhood psychosocial adversity has wide-ranging effects on neural, endocrine, immune, and metabolic physiology. Molecular mechanisms broadly implicate disruption of central neural networks, neuroendocrine stress dysregulation, and chronic inflammation, among other changes. Physiological disruption predisposes individuals to common diseases across the life course. Conclusions: Reviewed evidence has important implications for clinical practice, biomedical research, and work across other sectors relevant to public health and child wellbeing. Warranted changes include increased clinical screening for exposures among children and adults, scale-up of effective interventions, policy advocacy, and ongoing research to develop new evidence-based response strategies.