Evidence map›Paper›PMID 33362211›Full record

ArticlePloS one2020

Deficiency of mannose-binding lectin is a risk of Pneumocystis jirovecii pneumonia in a natural history cohort of people living with HIV/AIDS in Northern Thailand.

Kunio Yanagisawa, Nuanjun Wichukchinda, Naho Tsuchiya, Michio Yasunami, Archawin Rojanawiwat, Hidenori Tanaka, Hiroh Saji, Yoshiyuki Ogawa, Hiroshi Handa, Panita Pathipvanich and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
0.7field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Associations betweenJournal of fungi (Basel, Switzerland) · 2021
    Review
  5. Review
  6. 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

12 authors at 6 institutions in 2 countries.

Kunio YanagisawaDepartment of Hematology, Gunma University Hospital, Maebashi, Japan.ORCID 0000-0001-8542-7449
Nuanjun WichukchindaDepartment of Medical Sciences, Ministry of Public Health, Nonthaburi, Thailand.
Naho TsuchiyaDepartment of Preventive Medicine and Epidemiology, Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.
Michio YasunamiDepartment of Laboratory Medicine, Saga-Ken Medical Centre Koseikan, Saga, Japan.
Archawin RojanawiwatDepartment of Medical Sciences, Ministry of Public Health, Nonthaburi, Thailand.
Hidenori TanakaHLA Foundation Laboratory, Kyoto, Japan.
Hiroh SajiHLA Foundation Laboratory, Kyoto, Japan.
Yoshiyuki OgawaDepartment of Hematology, Gunma University Hospital, Maebashi, Japan.
Hiroshi HandaDepartment of Hematology, Gunma University Hospital, Maebashi, Japan.ORCID 0000-0003-3753-9862
Panita PathipvanichDay Care Centre, Lampang Hospital, Lampang, Thailand.
Koya AriyoshiDepartment of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Pathom SawanpanyalertDepartment of Medical Sciences, Ministry of Public Health, Nonthaburi, Thailand.
Gunma University Hospital · JPMinistry of Public Health · THLampang Hospital · THNagasaki University · JPSaga-Ken Medical Centre Koseikan · JPTohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMannose-binding lectin (MBL) plays a pivotal role in innate immunity; however, its impact on susceptibility to opportunistic infections (OIs) has not yet been examined in a natural history cohort of people living with HIV/AIDS.

methodsWe used archived samples to analyze the association between MBL expression types and risk of major OIs including Pneumocystis jirovecii pneumonia (PCP), cryptococcosis, talaromycosis, toxoplasmosis, and tuberculosis in a prospective cohort in Northern Thailand conducted from 1 July 2000 to 15 October 2002 before the national antiretroviral treatment programme was launched.

resultsOf 632 patients, PCP was diagnosed in 96 (15.2%) patients, including 45 patients with new episodes during the follow-up period (1006.5 person-years). The total history of PCP was significantly associated with low MBL expression type: high/intermediate (81/587, 13.8%), low (10/33, 30.3%) and deficient (5/12, 41.7%) (p = 0.001), whereas the history of other OIs showed no relation with any MBL expression type. Kaplan-Meier analysis (n = 569; log-rank p = 0.011) and Cox's proportional hazards model revealed that deficient genotype dramatically increased the risk of PCP, which is independent upon sex, age, CD4 count, HIV-1 viral load and hepatitis B and C status (adjusted hazard ratio 7.93, 95% confidence interval 2.19-28.67, p = 0.002).

conclusionsDeficiency of MBL expression is a strong risk factor determining the incidence of PCP but not other major OIs.

Indexed as

AdolescentAdultAIDS-Related Opportunistic InfectionsFemaleFollow-Up StudiesGenetic Predisposition to DiseaseGenotyping TechniquesHumansImmunity, InnateIncidenceMaleMannose-Binding LectinMiddle AgedPneumocystis cariniiPneumonia, PneumocystisProspective StudiesMannose-Binding LectinMBL2 protein, human

Identifiers

PMID33362211
PMCPMC7757797
OpenAlexW3113481410

What OpenQuestion holds

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LicenceCC BY
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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.