Evidence map›Paper›PMID 26208220›Full record

ArticlePloS one2015

Long-Term Trends in Esophageal Candidiasis Prevalence and Associated Risk Factors with or without HIV Infection: Lessons from an Endoscopic Study of 80,219 Patients.

Yuta Takahashi, Naoyoshi Nagata, Takuro Shimbo, Takeshi Nishijima, Koji Watanabe, Tomonori Aoki, Katsunori Sekine, Hidetaka Okubo, Kazuhiro Watanabe, Toshiyuki Sakurai and 13 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 72 citations in OpenAlex.

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  12. Prevalence and risk factors forWorld journal of clinical cases · 2022
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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

23 authors at 2 institutions in 1 country.

Yuta TakahashiDepartment of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Tokyo, Japan.
Naoyoshi NagataDepartment of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Tokyo, Japan.
Takuro ShimboOhta Nishinouchi Hospital, Fukushima, Japan.
Takeshi NishijimaDivision of AIDS Clinical Center (ACC), National Center for Global Health and Medicine, Tokyo, Japan.
Koji WatanabeDivision of AIDS Clinical Center (ACC), National Center for Global Health and Medicine, Tokyo, Japan.
Tomonori AokiDepartment of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Tokyo, Japan.
Katsunori SekineDepartment of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Tokyo, Japan.
Hidetaka OkuboDepartment of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Tokyo, Japan.
Kazuhiro WatanabeDivision of AIDS Clinical Center (ACC), National Center for Global Health and Medicine, Tokyo, Japan.
Toshiyuki SakuraiDepartment of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Tokyo, Japan.
Chizu YokoiDepartment of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Tokyo, Japan.
Masao KobayakawaDepartment of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Tokyo, Japan.
Hirohisa YazakiDivision of AIDS Clinical Center (ACC), National Center for Global Health and Medicine, Tokyo, Japan.
Katsuji TeruyaDivision of AIDS Clinical Center (ACC), National Center for Global Health and Medicine, Tokyo, Japan.
Hiroyuki GatanagaDivision of AIDS Clinical Center (ACC), National Center for Global Health and Medicine, Tokyo, Japan.
Yoshimi KikuchiDivision of AIDS Clinical Center (ACC), National Center for Global Health and Medicine, Tokyo, Japan.
Sohtaro MineDepartment of Pathology, National Center for Global Health and Medicine, Tokyo, Japan.
Toru IgariDepartment of Pathology, National Center for Global Health and Medicine, Tokyo, Japan.
Yuko TakahashiDivision of Rheumatic Diseases, National Center for Global Health and Medicine, Tokyo, Japan.
Akio MimoriDivision of Rheumatic Diseases, National Center for Global Health and Medicine, Tokyo, Japan.
Shinichi OkaDivision of AIDS Clinical Center (ACC), National Center for Global Health and Medicine, Tokyo, Japan.
Junichi AkiyamaDepartment of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Tokyo, Japan.
Naomi UemuraDepartment of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Kohnodai Hospital, Chiba, Japan.
National Center for Global Health and Medicine · JPOhta Nishinouchi Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prevalence of candida esophagitis (CE) might be changing in an era of highly active antiretroviral therapy (HAART) among HIV-infected patients or today's rapidly aging society among non-HIV-infected patients. However, few studies have investigated long-term CE trends, and CE risk factors have not been studied in a large sample, case-control study. This study aimed to determine long-term trends in CE prevalence and associated risk factors for patients with or without HIV infection.

methodsTrends in CE prevalence were explored in a cohort of 80,219 patients who underwent endoscopy between 2002 and 2014. Risks for CE were examined among a subcohort of 6,011 patients. In risk analysis, we assessed lifestyles, infections, co-morbidities, immunosuppressants, and proton-pump inhibitors (PPIs). All patients were tested for HIV, hepatitis B or C virus, and syphilis infection. For HIV-infected patients, sexual behavior, CD4 cell count, history of HAART were also assessed.

resultsCE prevalence was 1.7% (1,375/80,219) in all patients, 9.8% (156/1,595) in HIV-infected patients, and 1.6% (1,219/78,624) in non-HIV-infected patients. CE prevalence from 2002-2003 to 2012-2014 tended to increase in non-HIV-infected patients (0.6% to 2.5%; P<0.01) and decrease in HIV-infected patients (13.6% to 9.0%; P=0.097). Multivariate analysis revealed increasing age (odds ratio [OR], 1.02; p=0.007), HIV infection (OR, 4.92; p<0.001), and corticosteroid use (OR, 5.90; p<0.001) were significantly associated with CE, and smoking (OR, 1.32; p=0.085) and acetaminophen use (OR, 1.70; p=0.097) were marginally associated. No significant association was found with alcohol consumption, hepatitis B or C virus, syphilis, diabetes mellitus, cardiovascular disease, cerebrovascular disease, chronic kidney disease, liver cirrhosis, anticancer, or PPIs use. In HIV-infected patients, CD4 cell count <100/μL (OR, 4.83; p<0.001) and prior HAART (OR, 0.35; p=0.006) were independently associated with CE, but sexual behavior was not. Among corticosteroid users, CE was significantly associated with higher prednisone-equivalent dose (p=0.043 for trend test).

conclusionsThis large, endoscopy-based study demonstrated that CE prevalence increased in non-HIV-infected patients but decreased in HIV-infected patients over 13 years. Risk analysis revealed that increasing age, HIV infection, and corticosteroids use, particularly at higher doses, were independently associated with CE, but alcohol, other infections, diabetes, anticancer drugs, and PPIs use were not.

Indexed as

CoinfectionAgedAged, 80 and overCandidiasisCase-Control StudiesEndoscopy, Digestive SystemEsophagitisFemaleHIV InfectionsHumansMaleMiddle AgedOdds RatioPrevalence

Identifiers

PMID26208220
PMCPMC4514810
OpenAlexW1009742808

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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.