Evidence map›Paper›PMID 38816598›Full record

ArticleDigestive diseases and sciences2024

Increased Risk of Herpes Zoster Infection in Patients with Celiac Disease 50 Years Old and Older.

Arjun Chatterjee, Vibhu Chittajallu, Andrew Ford, Khaled Alsabbagh Alchirazi, Rama Nanah, Emad Mansoor, Sarah DeLozier, Claire Jansson-Knodell, Alberto Rubio-Tapia

Abstract read
In one paragraph

Article in Digestive diseases and sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Observational
  3. 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

9 authors.

Arjun ChatterjeeDepartment of Internal Medicine, Cleveland Clinic Foundation, Cleveland, OH, 44195, USA.
Vibhu ChittajalluDigestive Health Institute, Case Western Reserve University/University Hospitals Cleveland Medical Center, Cleveland, OH, USA.
Andrew FordDepartment of Internal Medicine, Cleveland Clinic Foundation, Cleveland, OH, 44195, USA.
Khaled Alsabbagh AlchiraziDepartment of Internal Medicine, Cleveland Clinic Foundation, Cleveland, OH, 44195, USA.
Rama NanahDepartment of Internal Medicine, Cleveland Clinic Foundation, Cleveland, OH, 44195, USA.
Emad MansoorDigestive Health Institute, Case Western Reserve University/University Hospitals Cleveland Medical Center, Cleveland, OH, USA.
Sarah DeLozierClinical Research Center, University Hospitals Cleveland Medical Center, Cleveland, OH, USA.
Claire Jansson-KnodellDigestive Disease and Surgery Institute, Cleveland Clinic Foundation, Cleveland, OH, 44195, USA.
Alberto Rubio-TapiaDigestive Disease and Surgery Institute, Cleveland Clinic Foundation, Cleveland, OH, 44195, USA. RUBIOTA@ccf.org.ORCID http://orcid.org/0000-0001-6964-4072

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCeliac Disease (CD) is associated with increased susceptibility to certain bacterial and viral infections. Herpes zoster (HZ) is a viral infection that can be prevented by immunization. In the US, the vaccine is recommended for adults ≥ 50 or ≥ 19 with certain at-risk conditions, not including CD.

aimsWe aimed to determine if adult patients aged < 50 or ≥ 50 years with CD had a higher risk of developing HZ.

methodsWe designed a retrospective cohort study. CD was defined as patients with the ICD-10 code for CD and positive Celiac serology. Patients with negative serology and lacking CD ICD-10 codes served as controls. Patients who had HZ before CD diagnosis were excluded. We formed two sub-cohorts, those aged < 50 (cohort 1) and aged ≥ 50 years (cohort 2), and evaluated HZ infection at 10-year follow-up. To account for confounding variables, we performed 1:1 propensity score matching (PSM).

resultsFollowing PSM, cohort 1 had 6,826 CD patients, and cohort 2 had 5,337 CD patients and respective matched controls. After ten years of follow-up, in cohort 1, 62 CD patients developed HZ versus 57 controls, RR: 1.09 (CI: 0.76-1.56, p-value = 0.64). In cohort 2, 200 CD patients developed HZ versus 159 controls, RR: 1.2 (CI: 1.02-1.54, p-value = 0.03).

conclusionThere was no significant difference in the likelihood of getting HZ in CD patients < 50, although CD patients ≥ 50 had a modestly increased risk. Our findings do not support routine early vaccination for HZ in CD, and the vaccine should be offered at age 50.

Indexed as

Celiac DiseaseHerpes ZosterAdultAgedAge FactorsFemaleHumansMaleMiddle AgedPropensity ScoreRetrospective StudiesRisk FactorsCeliac diseaseHerpes zosterImmunizationShinglesVaccine

Identifiers

PMID38816598
PMCPMC11341706

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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.