Evidence map›Paper›PMID 37808933›Full record

ReviewHealth science reports2023

Homozygote drepanocytosis: Ferric status and inflammation in world and Africa: Review article and meta analysis.

Romaric Tuono De Manfouo, Josué Simo Louokdom, Bernard Claude Chetcha, Prosper Cabral Biapa Nya, Constant Anatole Pieme, Claude Tayou Tagny

Open access · goldAbstract readReview
In one paragraph

Review in Health science reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 22% of its field
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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
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

6 authors at 3 institutions in 1 country.

Romaric Tuono De ManfouoDepartment of Microbiology, Parasitology, Hematology, and Infectious Diseases, Faculty of Medicine and Biomedical Sciences Université de Yaoundé 1 Yaoundé Cameroon.ORCID 0000-0002-2867-0538
Josué Simo LouokdomDepartment of Medicine, Pharmacy, and Biomedical Sciences, Higher Institute of Health Sciences Université des Montagnes Bangangté Cameroon.
Bernard Claude ChetchaDepartment of Microbiology, Parasitology, Hematology, and Infectious Diseases, Faculty of Medicine and Biomedical Sciences Université de Yaoundé 1 Yaoundé Cameroon.
Prosper Cabral Biapa NyaDepartment Biochemistry, Faculty of Sciences Université de Dschang Dschang Cameroon.ORCID 0000-0003-4830-9966
Constant Anatole PiemeDepartment of Microbiology, Parasitology, Hematology, and Infectious Diseases, Faculty of Medicine and Biomedical Sciences Université de Yaoundé 1 Yaoundé Cameroon.
Claude Tayou TagnyDepartment of Microbiology, Parasitology, Hematology, and Infectious Diseases, Faculty of Medicine and Biomedical Sciences Université de Yaoundé 1 Yaoundé Cameroon.
Université de Yaoundé I · CMUniversité de Dschang · CMUniversité des Montagnes · CM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Major sickle cell syndromes are subjected to a high frequency of hemolysis, infections, oxidative stress, and vasooclusive crises which promote inflammation and iron balance disorders. We aimed to systematically review and analyze the studies in this patients addressing in general, and Africa in particular. Methods: The systematic review of published articles in the Pubmed and Google Scholar databases was carried out according to the recommendations of the PRISMA model. The case-control articles have been included. The data extracted from the articles were analyzed using statistical software R. The standardized mean difference (SMD) was used to assess the extent of the disease on the different variables studied. Results: At the end, 128 articles were obtained; but only 33 were elligible for meta-analysis. A SMD of -1.79 was obtained for hemoglobin between the sickle cell patients and the controls due to the deviation from the overall mean hemoglobin in the cases (8 ± 2 g/dL) and in controls (13 ± 3 g/dL). Sickle cell disease showed a significant extent on ferritin [SMD = 2.61; (95% confidence interval, CI: 2.39-2.83); ( Conclusion: Patients with major sickle cell syndrome in inflammation have a higher risk of iron profile disorders compared to the normal population. Further studies are needed to explore mechanisms for preventing the deleterious effects of iron from this hemolysis, for example haptoglobin genotyping.

Indexed as

ferritinhemoglobinhemolysisinflammationserum ironsickle cell anemia

Identifiers

PMID37808933
PMCPMC10551275
OpenAlexW4387361519

What Socratic holds

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LicenceCC BY-NC
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Registered trials

None linked

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 Socratic graph.