Evidence map›Paper›PMID 27393914›Full record

ArticlePediatric blood & cancer2016

Cognitive functioning in children from Nigeria with sickle cell anemia.

Olubusola B Oluwole, Robert B Noll, Daniel G Winger, Olu Akinyanju, Enrico M Novelli

Abstract read
In one paragraph

Article in Pediatric blood & cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Trial
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  8. Dementia in Africa: Current evidence, knowledge gaps, and future directions.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2022
    Review
  9. Article
  10. Article
  11. Social-environmental factors and cognitive and behavioral functioning in pediatric sickle cell disease.Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence · 2020
    Article
  12. Article
  13. Associations of transcranial doppler velocity, age, and gender with cognitive function in children with sickle cell anemia in Nigeria.Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence · 2019
    Article
  14. Article
  15. Article
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

5 authors.

Olubusola B OluwoleSchool of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Robert B NollDepartment of Pediatrics, University of Pittsburgh, Pittsburgh, Pennsylvania.
Daniel G WingerClinical and Translational Science Institute, University of Pittsburgh, Pittsburgh, Pennsylvania.
Olu AkinyanjuSickle Cell Foundation Nigeria, Lagos, Nigeria.
Enrico M NovelliDivision of Hematology/Oncology, Department of Medicine, Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, Pennsylvania. noveex@upmc.edu.

Funding

University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
Neurovascular Determinants of Cognitive Function in Adults with Sickle Cell DiseaseR01HL127107 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NOVELLI, ENRICO M · 2016 to 2020
$3.6M
NCATS NIH HHS UL1 TR000005NHLBI NIH HHS R01 HL127107
6 · The paper itself

Abstract

backgroundCognitive impairment is a major neurological complication of sickle cell anemia (SCA) in the United States, but there are limited studies of cognitive impairment in Nigeria, the country with the highest SCA burden. We hypothesized that children from Nigeria with SCA have worse cognitive functioning than comparison children and explored the association between lower cognitive functioning and key laboratory demographic and socioeconomic variables among children with SCA. PROCEDURE: We conducted a cross-sectional survey, supplemented by anthropomorphic and laboratory data, among a convenience sample of children from Nigeria with and without SCA. We administered the Wechsler Intelligence Scale for Children, Version IV. Our primary outcome measures included (1) estimated IQ (Est. IQ), (2) working memory (WM), and (3) processing speed (PS).

resultsThe sample included 56 children with SCA (mean age 9.20 [SD 2.75], 46.43% girls) and 44 comparison children (mean age 9.41 [SD 2.49], 40.91% girls). Children with SCA performed worse on Est. IQ (84.58 vs. 96.10, P = 0.006) and PS (86.69 vs 96.91, P = 0.009) than comparison children. There was no significant difference in WM between both groups. Factors associated with lower Est. IQ and PS among children with SCA included age, maternal education, weight-for-age Z scores, and height-for age Z scores.

conclusionIn this small sample of children from Nigeria, we found worse cognitive functioning in children with SCA than in comparison children, and that sociodemographic and anthropomorphic factors were correlated with cognitive functioning.

Indexed as

CognitionAdolescentAnemia, Sickle CellChildCross-Sectional StudiesEducational StatusFemaleHumansIntelligenceMaleNigeriacognitive functioningIQNigerianutritionsickle cell anemia

Identifiers

PMID27393914
PMCPMC7134368

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Registered trials

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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.