Evidence map›Paper›PMID 25539285›Full record

ArticleChest2015

Serum Bilirubin and Disease Progression in Mild COPD.

Scott Apperley, Hye Yun Park, Daniel T Holmes, S F Paul Man, Donald Tashkin, Robert A Wise, John E Connett, Don D Sin

Open access · bronzeAbstract read
In one paragraph

Article in Chest, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

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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

8 authors at 6 institutions in 3 countries.

Scott ApperleyDepartment of Medicine, Pulmonary Division, University of British Columbia, Vancouver, BC, Canada.
Hye Yun ParkUBC James Hogg Research Centre and the Institute for Heart and Lung Health, St. Paul's Hospital, Vancouver, BC, Canada; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Samsung Medical Center, Seoul, South Korea.
Daniel T HolmesDepartment of Pathology, University of British Columbia, Vancouver, BC, Canada.
S F Paul ManDepartment of Medicine, Pulmonary Division, University of British Columbia, Vancouver, BC, Canada; UBC James Hogg Research Centre and the Institute for Heart and Lung Health, St. Paul's Hospital, Vancouver, BC, Canada.
Donald TashkinDivision of Pulmonary and Critical Care Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA.
Robert A WiseDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
John E ConnettDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN.
Don D SinDepartment of Medicine, Pulmonary Division, University of British Columbia, Vancouver, BC, Canada; UBC James Hogg Research Centre and the Institute for Heart and Lung Health, St. Paul's Hospital, Vancouver, BC, Canada. Electronic address: don.sin@hli.ubc.ca.
University of British Columbia · CAJohns Hopkins Medicine · USSamsung Medical Center · KRSt. Paul's Hospital · CAUniversity of California, Los Angeles · USUniversity of Minnesota · US

Funding

LUNG HEALTH STUDY--LONG TERM FOLLOW UPU10HL059274 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI WISE, ROBERT A. · 1998 to 2002
$283k
Canadian Institutes of Health Research
6 · The paper itself

Abstract

backgroundCOPD is a chronic inflammatory disorder associated with oxidative stress. Serum bilirubin has potent antioxidant actions, and higher concentrations have been shown to protect against oxidative stress. The relation between serum bilirubin and COPD progression is unknown.

methodsSerum bilirubin was measured in 4,680 smokers aged 35 to 60 years old with mild to moderate airflow limitation. The relationship of serum bilirubin to postbronchodilator FEV₁ and rate of FEV1 decline over 3 to 9 years was determined using regression modeling. Total and disease-specific mortality were also ascertained.

resultsSerum bilirubin was positively related to FEV₁ (P < .001). Serum bilirubin was also negatively related to the annual decline in FEV₁ when adjusted for baseline demographics, pack-years smoked, and baseline measures of lung function (P = .01). Additionally, serum bilirubin was negatively associated with risk of death from coronary heart disease (P = .03); however, the relationships between bilirubin and other mortality end points were not statistically significant (P > .05).

conclusionsBilirubin is inversely related to COPD disease severity and progression. Higher serum bilirubin concentration was associated with a higher FEV₁ and less annual decline in FEV₁. Bilirubin was also associated with less coronary heart disease mortality. These data support the hypothesis that bilirubin has a protective effect on COPD disease progression, possibly through its antioxidant actions. Bilirubin may prove useful as an easily accessible and readily available blood-based COPD biomarker.

Indexed as

Disease ProgressionAdultBilirubinCohort StudiesFemaleForced Expiratory VolumeHumansMaleMiddle AgedPulmonary Disease, Chronic ObstructiveSmokingSpirometryTime FactorsBilirubin

Identifiers

PMID25539285
PMCPMC4493872
OpenAlexW1712232958

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.