Evidence map›Paper›PMID 41253090›Full record

Trial reportNutrition research (New York, N.Y.)2025

Including malnourished siblings in treatment improves nutritional outcomes for children with sickle cell anemia in Northern Nigeria: Results from a feasibility trial.

Hassan Adam Murtala, Shehu U Abdullahi, Safiya Gambo, Halima Kabir, Khadija A Shamsu, Garba Gwarzo, Sari A Acra, Virginia A Stallings, Mark Rodeghier, Michael R DeBaun and 1 more

Registry-linked trialAbstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Nutrition research (New York, N.Y.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03634488 (Management of Severe Acute Malnutrition in Children With Sickle Cell Disease Greater Than 5 Years of Age Living in Northern Nigeria), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03634488 phase2completednot on this map

Management of Severe Acute Malnutrition in Children With Sickle Cell Disease Greater Than 5 Years of Age Living in Northern Nigeria

TypeinterventionalSponsorVanderbilt University Medical CenterRan2021 to 2022Enrolled132ConditionsSickle Cell Anemia, Severe Acute MalnutritionArmshydroxyurea (20mg/kg/day), Ready-to-use therapeutic food
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Hassan Adam MurtalaDepartment of Pediatrics, Murtala Muhammad Specialist Hospital, Kano, Nigeria.
Shehu U AbdullahiDepartment of Pediatrics, Bayero University/Aminu Kano Teaching Hospital, Kano, Nigeria.
Safiya GamboDepartment of Pediatrics, Murtala Muhammad Specialist Hospital, Kano, Nigeria.
Halima KabirDepartment of Pediatrics, Bayero University/Aminu Kano Teaching Hospital, Kano, Nigeria.
Khadija A ShamsuDepartment of Pediatrics, Bayero University/Aminu Kano Teaching Hospital, Kano, Nigeria.
Garba GwarzoDepartment of Pediatrics, Bayero University/Aminu Kano Teaching Hospital, Kano, Nigeria.
Sari A AcraDepartment of Pediatrics, D. Brent Polk Division of Pediatric Gastroenterology, Hepatology, and Nutrition at Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, TN, USA.
Virginia A StallingsDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, The Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, USA.
Mark RodeghierRodeghier Consultants, Chicago, IL, USA.
Michael R DeBaunDepartment of Pediatrics, Vanderbilt-Meharry Center of Excellence in Sickle Cell Disease, Vanderbilt University Medical Center, Nashville, TN, USA; Vanderbilt Institute for Global Health, Vanderbilt University Medical Center, Nashville, TN, USA.
Lauren J KleinDepartment of Pediatrics, D. Brent Polk Division of Pediatric Gastroenterology, Hepatology, and Nutrition at Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, TN, USA; Vanderbilt Institute for Global Health, Vanderbilt University Medical Center, Nashville, TN, USA. Electronic address: lauren.klein@vumc.org.

Funding

TRAINING IN GASTROENTEROLOGYT32DK007673 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 1992 to 2026
$8.4M
Vanderbilt-Emory-Cornell-Duke Global Health Fellowship Consortium-Expanding Diversity for Global Equity (EDGE)D43TW009337 · FIC · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALIYU, MUKTAR HASSAN, HEIMBURGER, DOUGLAS CORBETT · 2017 to 2021
$6.3M
Management of severe acute malnutrition in children with sickle cell disease greater than 5 years of age living in northern NigeriaR21HD097992 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ABDULLAHI, SHEHU UMAR, DEBAUN, MICHAEL R. · 2019 to 2020
$424k
FIC NIH HHS D43 TW009337NICHD NIH HHS R21 HD097992NIDDK NIH HHS T32 DK007673
6 · The paper itself

Abstract

Best treatment approaches for malnutrition in children with sickle cell anemia (SCA) remain underexplored. We hypothesized that (1) children with SCA (CwSCA) enrolled in a malnutrition trial alongside their non-SCA siblings would experience greater nutritional improvements than those without an enrolled sibling and (2) enrolled malnourished siblings without SCA would have higher baseline nutritional status and greater improvements in nutritional status than CwSCA. We tested these hypotheses as part of a randomized controlled feasibility trial at 2 medical centers in northern Nigeria, a low-resource setting with a significant burden of malnutrition and SCA. Participants included 108 CwSCA (5-12 years) with severe malnutrition (body mass index (BMI) z-score <-3.0), 21 of whom had an enrolled sibling (Sibling) with severe malnutrition but without SCA (5-12 years, n = 22). All participants received daily ready-to-use therapeutic food (RUTF) for 12 weeks. CwSCA with a Sibling had a higher mean BMI z-score change than CwSCA without a Sibling (0.8 vs 0.4, P = .003). The mean baseline BMI z-scores for the CwSCA (-3.7) were comparable to those of their Siblings (-3.6; P = .47). Improvement in BMI z-score was similar between CwSCA and their malnourished siblings without SCA. In conclusion, our findings suggest that including malnourished siblings in nutritional interventions enhances outcomes for CwSCA. We postulate that the additional calories delivered by co-treating siblings reduce intrahousehold competition for RUTF, thereby allowing CwSCA to consume a greater share of the therapeutic food. This trial was registered at clinicaltrials.gov (NCT03634488).

Indexed as

Anemia, Sickle CellChild Nutrition DisordersMalnutritionNutritional StatusSiblingsBody Mass IndexChildChild, PreschoolFeasibility StudiesFemaleHumansMaleNigeriaTreatment OutcomeBody mass indexChild nutrition disordersMalnutritionSiblingsSickle cell anemia

Identifiers

PMID41253090
PMCPMC13221909

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Registered trials

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.