Evidence map›Paper›PMID 41170221›Full record

ArticleCureus2025

Framing Childhood Anemia as an Adverse Childhood Experiences-Associated Health Condition: An Opportunity to Support Healthy Growth and Development.

Beckett Z Hutchens, Joseph P Benitez, Nina Thompson, Kelsi E McCoy-Wilson, Randall Chan, Amy J Shekarchi

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Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Beckett Z HutchensDepartment of Pediatrics, University of California Los Angeles David Geffen School of Medicine, Los Angeles, USA.
Joseph P BenitezDepartment of Pediatrics, University of California Los Angeles David Geffen School of Medicine, Los Angeles, USA.
Nina ThompsonACEs-LA, Los Angeles County Department of Health Services, Los Angeles, USA.
Kelsi E McCoy-WilsonDepartment of Pediatrics, University of California Los Angeles David Geffen School of Medicine, Los Angeles, USA.
Randall ChanDepartment of Pediatrics, University of Southern California Keck School of Medicine, Los Angeles, USA.
Amy J ShekarchiDepartment of Pediatrics, University of California Los Angeles David Geffen School of Medicine, Los Angeles, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionBoth childhood adversity and childhood anemia have the potential to impact growth and development among young children. This study examined the relationship between Adverse Childhood Experience (ACE) scores and hemoglobin levels in young children receiving care in a safety net health system in California.

methodsWe conducted a retrospective review of electronic health records for pediatric patients ages zero to five years who received both ACE screening and hemoglobin testing between 2020 and 2025. Hemoglobin results were categorized as severe anemia (<7.0 mg/dl), mild-moderate anemia (7.0-10.9 mg/dl), and normal (>11.0 mg/dl). ACE scores were categorized into Low-Intermediate Risk (ACE score 0-3) and High Risk (ACE score ≥4).

resultsWe found an association between higher ACEs and lower hemoglobin levels across all patients and within the subset of patients with mild-moderate anemia. Among a population of 8,979, 21.7% had any ACE, 18.3% reported ACE scores of 1-3, and 3.4% had ACE scores of ≥4. Mean hemoglobin was lower in the ACEs High Risk group compared to the ACEs Low-Intermediate Risk group (12.2 mg/dl vs. 12.6 mg/dl, p < 0.001). In the subgroup with mild-moderate anemia (N = 716), ACEs High Risk children also had lower mean hemoglobin levels (9.9 mg/dl vs. 10.3 mg/dl, p < 0.05). Moreover, linear regression models showed that each one-point increase in ACE score resulted in a 0.078 mg/dl decrease in mean hemoglobin (p < 0.0001). DISCUSSION: While statistically significant, the 0.4 mg/dl difference in hemoglobin levels alone does not often have clinical implications for treatment. However, in the context of high ACE scores, this difference may help guide preventative and treatment efforts.

conclusionsThe association of higher ACE scores with lower hemoglobin levels in young children highlights an opportunity to better identify factors that may contribute to anemia in pediatric patients. Knowledge of such risk factors can inform efforts to provide comprehensive counseling and support for patients at risk for anemia. Further research will help determine whether integrating ACE screening into anemia prevention strategies could impact developmental and health outcomes in high-risk populations, and this inquiry may further establish childhood anemia as a meaningful ACE-associated health condition that can be identified and addressed before long-term health consequences emerge.

Indexed as

ace-associated health conditionadverse childhood experienceadverse childhood experiences (aces)childhood anemiafood insecurityiron deficiencypediatric preventive care

Identifiers

PMID41170221
PMCPMC12571428

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.