Evidence map›Paper›PMID 37090544›Full record

ArticlemedRxiv : the preprint server for health sciences2023

Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency and Long-Term Risk of Immune-Related diseases.

Ariel Israel, Alejandro A Schäffer, Matitiahu Berkovitch, David J Ozeri, Eugene Merzon, Ilan Green, Avivit Golan-Cohen, Eytan Ruppin, Shlomo Vinker, Eli Magen

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Ariel IsraelLeumit Research Institute, Leumit Health Services, Tel Aviv-Yafo 6473817, Israel.
Alejandro A SchäfferCancer Data Science Laboratory, National Cancer Institute, Bethesda, MD 20892, USA.
Matitiahu BerkovitchClinical Pharmacology and Toxicology Unit, Shamir Medical Center, Zerifin.
David J OzeriLeumit Research Institute, Leumit Health Services, Tel Aviv-Yafo 6473817, Israel.
Eugene MerzonLeumit Research Institute, Leumit Health Services, Tel Aviv-Yafo 6473817, Israel.
Ilan GreenLeumit Research Institute, Leumit Health Services, Tel Aviv-Yafo 6473817, Israel.
Avivit Golan-CohenLeumit Research Institute, Leumit Health Services, Tel Aviv-Yafo 6473817, Israel.
Eytan RuppinCancer Data Science Laboratory, National Cancer Institute, Bethesda, MD 20892, USA.
Shlomo VinkerLeumit Research Institute, Leumit Health Services, Tel Aviv-Yafo 6473817, Israel.
Eli MagenLeumit Research Institute, Leumit Health Services, Tel Aviv-Yafo 6473817, Israel.
Tel Aviv University · ILNational Cancer Institute · USAriel University · ILAssaf Harofeh Medical Center · ILClalit Health Services · ILSheba Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked recessive enzymatic disorder, particularly prevalent in Africa, Asia and the Middle East. In the US, about 14% of black men are affected. Individuals with G6PD deficiency are often asymptomatic but may develop hemolysis following an infection or upon consumption of specific medications. Despite some evidence that G6PD deficiency affects the immune system, the long- term health risks associated with G6PD deficiency had not been studied in a large population.

methodsIn this retrospective cohort study, health records from G6PD deficient individuals were compared to matched controls in a national healthcare provider in Israel (Leumit Health Services). Rates of infectious diseases, allergic conditions and autoimmune disorders were compared between groups.

resultsThe cohort included 7,473 G6PD deficient subjects (68.7% men) matched with 29,892 control subjects (4:1 ratio) of the same age, gender, socioeconomic status and ethnic group, followed during 14.3±6.2 years.Significantly increased rates for autoimmune disorders, infectious diseases and allergic conditions were observed throughout this period. Notable increases were observed for rheumatoid arthritis (OR 2.41, p<0.001), systemic lupus erythematosus (OR 4.56, p<0.001), scleroderma (OR 6.87, p<0.001), pernicious anemia (OR=18.70, P<0.001), fibromyalgia (OR 1.98, p<0.001), Graves' disease (OR 1.46, P=0.001), and Hashimoto's thyroiditis (OR 1.26, P=0.001). These findings were corroborated with elevated rates of positive autoimmune serology and higher rates of treatment with medications commonly used to treat autoimmune conditions in the G6PD deficient group.

conclusionG6PD deficient individuals suffer from higher rates of autoimmune disorders, infectious diseases, and allergic conditions.

Identifiers

PMID37090544
PMCPMC10120794
OpenAlexW4360822134

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.