Evidence map›Paper›PMID 26584061›Full record

ArticleAmerican journal of respiratory cell and molecular biology2016

Age, Sexual Dimorphism, and Disease Associations in the Developing Human Fetal Lung Transcriptome.

Alvin T Kho, Divya Chhabra, Sunita Sharma, Weiliang Qiu, Vincent J Carey, Roger Gaedigk, Carrie A Vyhlidal, J Steven Leeder, Kelan G Tantisira, Scott T Weiss

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.8field-weighted citation impact, top 6% 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, 38 citations in OpenAlex.

  1. Trial
  2. Trial
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  4. Sex and the Developmental Environment Shape Molecular Networks Underlying Bronchial Responsiveness in Mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  5. Observational
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  18. Review
  19. Human lung development: recent progress and new challenges.Development (Cambridge, England) · 2018
    Review
  20. 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

10 authors at 2 institutions in 1 country.

Alvin T Kho1 Children's Hospital Informatics Program, Boston Children's Hospital, Boston, Massachusetts.
Divya Chhabra2 Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Sunita Sharma2 Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Weiliang Qiu2 Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Vincent J Carey2 Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Roger Gaedigk5 Division of Pediatric Clinical Pharmacology and Medical Toxicology, Children's Mercy Hospital and Clinics, Kansas City, Missouri; and.
Carrie A Vyhlidal5 Division of Pediatric Clinical Pharmacology and Medical Toxicology, Children's Mercy Hospital and Clinics, Kansas City, Missouri; and.
J Steven Leeder5 Division of Pediatric Clinical Pharmacology and Medical Toxicology, Children's Mercy Hospital and Clinics, Kansas City, Missouri; and.
Kelan G Tantisira2 Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Scott T Weiss2 Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Brigham and Women's Hospital · USChildren's Mercy Hospital · US

Funding

THE PHARMACOGENETICS OF ASTHMA TREATMENTU01HL065899 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI TANTISIRA, KELAN G, WEISS, SCOTT T · 2000 to 2014
$38.5M
SYSTEMS APPROACHES TO THE EPIDEMIOLOGY, GENETICS AND GENOMICS OF LUNG DISEASEST32HL007427 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI DAWN L DEMEO, Edwin K Silverman · 1985 to 2026
$13.6M
INTEGRATIVE PHARMACOGENOMICS OF LEUKOTRIENE INHIBITION IN ASTHMAR01HL092197 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI TANTISIRA, KELAN G · 2009 to 2013
$3.6M
INTRAUTERINE SMOKE EXPOSURE AND ASTHMA: GENOMIC ORIGINSR01HL097144 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI KOBZIK, LESTER, WEISS, SCOTT T · 2009 to 2013
$2.9M
A Developmental Basis for Chronic Obstructive Lung DiseaseK25HL091124 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI KHO, ALVIN THONG-JUAK · 2008 to 2012
$743k
INTEGRATIVE GENOMICS AND THE FETAL ORIGINS OF IMPAIRED LUNG FUNCTIONK08HL096833 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SHARMA, SUNITA · 2010 to 2013
$547k
CIGARETTE SMOKE IMPACTS FETAL LUNG DNA METHYLATION AND GENE EXPRESSIONR21HL107927 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI DEMEO, DAWN L, TANTISIRA, KELAN G · 2011 to 2012
$491k
NHLBI NIH HHS K08 HL096833NHLBI NIH HHS K25 HL091124NHLBI NIH HHS R01 HL092197NHLBI NIH HHS R01 HL097144NHLBI NIH HHS R21 HL107927NHLBI NIH HHS T32 HL007427NHLBI NIH HHS U01 HL065899
6 · The paper itself

Abstract

The fetal origins of disease hypothesis suggests that variations in the course of prenatal lung development may affect life-long pulmonary function growth, decline, and pathobiology. Many studies support the existence of differences in the developing lung trajectory in males and females, and sex-specific differences in the prevalence of chronic lung diseases, such as asthma and bronchopulmonary dysplasia. The objectives of this study were to investigate the early developing fetal lung for transcriptomic correlates of postconception age (maturity) and sex, and their associations with chronic lung diseases. We analyzed whole-lung transcriptome profiles of 61 females and 78 males at 54-127 days postconception (dpc) from nonsmoking mothers using unsupervised principal component analysis and supervised linear regression models. We identified dominant transcriptomic correlates for postconception age and sex with corresponding gene sets that were enriched for developing lung structural and functional ontologies. We observed that the transcriptomic sex difference was not a uniform global time shift/lag, rather, lungs of males appear to be more mature than those of females before 96 dpc, and females appear to be more mature than males after 96 dpc. The age correlate gene set was consistently enriched for asthma and bronchopulmonary dysplasia genes, but the sex correlate gene sets were not. Despite sex differences in the developing fetal lung transcriptome, postconception age appears to be more dominant than sex in the effect of early fetal lung developments on disease risk during this early pseudoglandular phase of development.

Indexed as

Sex CharacteristicsAge FactorsDatabases, GeneticFemaleFetusGene Expression ProfilingGene Expression Regulation, DevelopmentalHumansLungLung DiseasesMalePrincipal Component AnalysisStatistics as TopicTranscriptomeasthmabronchopulmonary dyplasiaembryonic and fetal developmentlungsex dimorphism

Identifiers

PMID26584061
PMCPMC4942221
OpenAlexW2173765536

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.