Evidence map›Paper›PMID 33502483›Full record

ArticleJAMA network open2021

Association of Serum Mannose With Acute Respiratory Distress Syndrome Risk and Survival.

Yongyue Wei, Hui Huang, Ruyang Zhang, Zhaozhong Zhu, Ying Zhu, Lijuan Lin, Xuesi Dong, Liangmin Wei, Xin Chen, Zhonghua Liu and 4 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in JAMA network open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Causal Associations Between Human Blood Metabolites and Cardio-Cerebrovascular Diseases: A Mendelian Randomisation Study.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    Article
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

14 authors at 3 institutions in 3 countries.

Yongyue WeiDepartment of Biostatistics, Nanjing Medical University School of Public Health, Nanjing, Jiangsu, China.
Hui HuangDepartment of Biostatistics, Nanjing Medical University School of Public Health, Nanjing, Jiangsu, China.
Ruyang ZhangDepartment of Biostatistics, Nanjing Medical University School of Public Health, Nanjing, Jiangsu, China.
Zhaozhong ZhuDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
Ying ZhuDepartment of Biostatistics, Nanjing Medical University School of Public Health, Nanjing, Jiangsu, China.
Lijuan LinDepartment of Biostatistics, Nanjing Medical University School of Public Health, Nanjing, Jiangsu, China.
Xuesi DongDepartment of Biostatistics, Nanjing Medical University School of Public Health, Nanjing, Jiangsu, China.
Liangmin WeiDepartment of Biostatistics, Nanjing Medical University School of Public Health, Nanjing, Jiangsu, China.
Xin ChenDepartment of Biostatistics, Nanjing Medical University School of Public Health, Nanjing, Jiangsu, China.
Zhonghua LiuDepartment of Statistics and Actuarial Science, The University of Hong Kong, Hong Kong, China.
Yang ZhaoDepartment of Biostatistics, Nanjing Medical University School of Public Health, Nanjing, Jiangsu, China.
Li SuDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
Feng ChenDepartment of Biostatistics, Nanjing Medical University School of Public Health, Nanjing, Jiangsu, China.
David C ChristianiDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
Nanjing Medical University · CNHarvard University · USUniversity of Hong Kong · HK

Funding

Translational Research Support CoreP30ES000002 · NIEHS · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI JAIME ELIZABETH HART · 1985 to 2026
$44.6M
MOLECULAR EPIDEMIOLOGY OF ARDSR01HL060710 · NHLBI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI CHRISTIANI, DAVID C · 2000 to 2015
$8.4M
Molecular and Genetic Analysis of Lung Cancer SurvivalR01CA092824 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI CHRISTIANI, DAVID C · 2002 to 2013
$5.9M
NCI NIH HHS R01 CA092824NHLBI NIH HHS R01 HL060710NIEHS NIH HHS P30 ES000002
6 · The paper itself

Abstract

Importance: Acute respiratory distress syndrome (ARDS) confers high mortality risk among critically ill patients. Identification of biomarkers associated with ARDS risk may guide clinical diagnosis and prognosis. Objective: To systematically evaluate the association of blood metabolites with ARDS risk and survival. Design, Setting, and Participants: In this cohort study, data from the Molecular Epidemiology of ARDS (MEARDS) study, a prospective cohort of 403 patients with ARDS and 1227 non-ARDS controls, were analyzed. Patients were recruited in intensive care units (ICUs) at Massachusetts General Hospital and Beth Israel Deaconess Medical Center, both in Boston, Massachusetts, from January 1, 1998, to December 31, 2014. Data analysis was performed from December 9, 2018, to January 4, 2019. Main Outcomes and Measures: Participants were followed up daily for ARDS development defined by Berlin criteria, requiring fulfillment of chest radiograph and oxygenation criteria on the same calendar day during invasive ventilatory assistance. A 2-stage study design was used to explore novel metabolites associated with ARDS risk and survival. Results: Of the 1630 participants from MEARDS who were admitted to the ICU , 403 (24.7%) were diagnosed with ARDS (mean [SD] age, 63.0 [17.0] years; 251 [62.3%] male) and 1227 (75.3%) were at-risk but did not have ARDS (mean [SD] age, 62.3 [16.9] years; 753 [61.4%] male). Mendelian randomization suggested that genetically regulated serum mannose was associated with ARDS risk (odds ratio [OR], 0.64; 95% CI, 0.53-0.78; P = 7.46 × 10-6) in the discovery stage. In the functional validation stage incorporating 83 participants with ARDS and matched at-risk participants in the control group from the ICU, the protective association of mannose with ARDS risk was validated (OR, 0.67; 95% CI, 0.46-0.97; P = .03). Furthermore, serum mannose was associated with 28-day (OR, 0.25; 95% CI, 0.11-0.56; P = 6.95 × 10-4) and 60-day (OR, 0.36; 95% CI, 0.19-0.71; P = 3.12 × 10-3) mortality and 28-day (hazard ratio, 0.49; 95% CI, 0.32-0.74; P = 6.41 × 10-4) and 60-day (hazard ratio, 0.55; 95% CI, 0.37-0.80; P = 2.11 × 10-3) survival. Conclusions and Relevance: In this study, genetically regulated serum mannose appeared to be associated with ARDS risk and outcome, and increased serum mannose at admission was associated with reduced ARDS risk and better survival. These findings could inform prevention and clinical intervention in ARDS cases, which have increased with the expansion of the coronavirus disease 2019 pandemic.

Indexed as

AgedAPACHECritical IllnessFemaleHumansIntensive Care UnitsLogistic ModelsMaleMannoseMendelian Randomization AnalysisMiddle AgedPatient AdmissionPrognosisProportional Hazards ModelsProspective StudiesRespiratory Distress SyndromeMannose

Identifiers

PMID33502483
PMCPMC7841460
OpenAlexW3124061202

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.