Evidence map›Paper›PMID 39008448›Full record

ArticlePloS one2024

Association between fetal hemoglobin, lactate dehydrogenase, and disease severity in patients with sickle cell disease at Bugando Medical Centre, Mwanza, Tanzania.

Samwel Edward Kahema, Cosmas H Mbulwa, Charles Nkubi Bagenda, Nixon Niyonzima, Enoch Muwanguzi, Tunzo L Mcharo

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In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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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

2 citing papers in PubMed.

  1. Article
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4 · The record

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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.

Samwel Edward KahemaMbarara University of Science and Technology, Mbarara, Uganda.ORCID 0009-0008-5176-869X
Cosmas H MbulwaBugando Medical Centre, Mwanza, Tanzania.
Charles Nkubi BagendaMbarara University of Science and Technology, Mbarara, Uganda.ORCID 0009-0006-4235-1003
Nixon NiyonzimaUganda Cancer Institute, Kampala, Uganda.
Enoch MuwanguziMbarara University of Science and Technology, Mbarara, Uganda.
Tunzo L McharoJakaya Kikwete Cardiac Institute, Dar es Salaam, Tanzania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThere is a wide range of clinical manifestations in sickle cell disease (SCD). Despite having the same condition, each person's response to disease complications differs greatly. Individuals can be categorized according to the severity of their diseases to determine which group they fall into and receive the appropriate care based on their needs. The relationship between fetal hemoglobin (HbF), lactate dehydrogenase (LDH), and disease severity in Tanzania is little understood. This investigation sought to ascertain the relationship between HbF, LDH, and disease severity in SCD patients at the Bugando Medical Center.

methodThis cross-sectional study was carried out on SCD patients aged 6 months and older at the Bugando Medical Center in Mwanza, Tanzania. A total of 130 SCD patients were enrolled. The clinical history and laboratory test results for SCD patients were recorded on a specially constructed patient report form.

resultsThe majority of participants (56.9%) were men. For the population under study, more than half (60.8%) of participants had a moderate clinical phenotype (MCP), followed by 31.5% of asymptomatic participants and 7.7% of people with severe clinical phenotypes (SCP). Participants with SCP had substantially higher levels of LDH, with a mean level of 810.97IU/L (95% CI: 559.31-1062.64) and a p-value of 0.005. The severe clinical phenotype exhibited a significantly higher mean HbF score value of 10.09% (95% CI: 7.44-13.74%) with a p-value of 0.024 when compared to the asymptomatic and moderate clinical phenotypes.

conclusionIn SCD patients with SCP compared to ACP and MCP, the HbF levels were higher, but did not show a protective effects, and LDH can be used to predict the severity of SCD.

Indexed as

Anemia, Sickle CellFetal HemoglobinL-Lactate DehydrogenaseSeverity of Illness IndexAdolescentAdultChildChild, PreschoolCross-Sectional StudiesFemaleHumansInfantMaleMiddle AgedTanzaniaYoung AdultFetal HemoglobinL-Lactate Dehydrogenase

Identifiers

PMID39008448
PMCPMC11249230

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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.