Evidence map›Paper›PMID 42627583›Full record

ArticleImmunologic research2026

Hidden Burden: Liver and Gastrointestinal Involvement in Chronic Granulomatous Disease.

Zehra Genç Ozbay, Saliha Esenboga, Elif Soyak Aytekin, Deniz İlgün Gürel, Ersin Gümüş, Hayriye Hizarcioglu Gulsen, Barış Kuşkonmaz, İnci Nur Saltık-Temizel, Hasan Özen, Hülya Demir and 1 more

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Article in Immunologic research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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.

No citing paper in PubMed yet.

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

11 authors.

Zehra Genç OzbayDivision of Pediatric Immunology, Department of Pediatrics, Hacettepe University Medical School, Ankara, Turkey.
Saliha EsenbogaDivision of Pediatric Immunology, Department of Pediatrics, Hacettepe University Medical School, Ankara, Turkey. salihaeren@yahoo.com.ORCID http://orcid.org/0000-0003-0562-9863
Elif Soyak AytekinDivision of Pediatric Immunology, Department of Pediatrics, Hacettepe University Medical School, Ankara, Turkey.
Deniz İlgün GürelDivision of Pediatric Immunology, Department of Pediatrics, Hacettepe University Medical School, Ankara, Turkey.
Ersin Gümüşİhsan Doğramacı Children's Hospital, Hacettepe University, Altındağ, Ankara, 06100, Turkey.
Hayriye Hizarcioglu Gulsenİhsan Doğramacı Children's Hospital, Hacettepe University, Altındağ, Ankara, 06100, Turkey.
Barış Kuşkonmazİhsan Doğramacı Children's Hospital, Hacettepe University, Altındağ, Ankara, 06100, Turkey.
İnci Nur Saltık-Temizelİhsan Doğramacı Children's Hospital, Hacettepe University, Altındağ, Ankara, 06100, Turkey.
Hasan Özenİhsan Doğramacı Children's Hospital, Hacettepe University, Altındağ, Ankara, 06100, Turkey.
Hülya Demirİhsan Doğramacı Children's Hospital, Hacettepe University, Altındağ, Ankara, 06100, Turkey.
Deniz CagdasDivision of Pediatric Immunology, Department of Pediatrics, Hacettepe University Medical School, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by defective reactive oxygen species production, leading to recurrent infections, chronic inflammation, and immune dysregulation. Hepatic and gastrointestinal (GI) involvement are major contributors to disease-related morbidity. To evaluate hepatic and GI involvement in patients with CGD and to assess their associations with clinical features and outcomes. This retrospective single-center cohort study included 80 patients diagnosed with CGD between 1984 and 2025. Demographic, clinical, laboratory, genetic, and outcome data were analyzed. Hepatic and GI involvement were defined based on clinical, radiological, endoscopic, and histopathological findings. The cohort was predominantly male (63.8%), with a median age at diagnosis of 3.5 years and a high rate of parental consanguinity (62.5%). Hepatic involvement was identified in 52.5% of patients, most commonly hepatomegaly (42.5%), followed by hepatic abscesses (15%) and steatosis (11.3%). Gastrointestinal involvement was documented in 10% of patients, with inflammatory bowel disease (IBD) occurring in 8.8%, typically presenting with diarrhea, rectal bleeding, and abdominal pain. Growth failure (42.2% of children) and chronic diarrhea (21.3%) were also common clinical features. During follow-up, 17 patients (21.3%) died. Mortality was numerically higher among patients with hepatic involvement than among those without (26.2% vs. 15.8%), although the difference was not statistically significant. In exploratory multivariable Cox regression analysis, elevated alanine aminotransferase (ALT) levels at diagnosis were associated with mortality (HR 4.78, p = 0.020), whereas no independent predictors of hepatic or gastrointestinal involvement were identified. CGD is a complex disorder characterized by both susceptibility to infection and immune dysregulation. Hepatic and GI manifestations represent important components of the disease spectrum. Elevated ALT levels at the time of CGD diagnosis were associated with mortality in exploratory multivariable analysis, suggesting that baseline liver function assessment at diagnosis, together with longitudinal monitoring, may provide prognostic information, although this finding requires confirmation in larger prospective studies.

Indexed as

Gastrointestinal DiseasesGastrointestinal TractGranulomatous Disease, ChronicLiverLiver DiseasesAdolescentChildChild, PreschoolFemaleHumansInfantMalePrognosisRetrospective StudiesChronic granulomatous diseaseHepatic abscessImmune dysregulationInflammatory bowel diseaseLiver involvement

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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.