Evidence map›Paper›PMID 30859582›Full record

ArticleHepatology (Baltimore, Md.)2019

Collagen Formation Assessed by N-Terminal Propeptide of Type 3 Procollagen Is a Heritable Trait and Is Associated With Liver Fibrosis Assessed by Magnetic Resonance Elastography.

Cyrielle Caussy, Meera Bhargava, Ida F Villesen, Natasja S Gudmann, Diana J Leeming, Morten A Karsdal, Claire Faulkner, Denny Bao, Amy Liu, Min-Tzu Lo and 7 more

Open access · greenAbstract readTwin Study
In one paragraph

Article in Hepatology (Baltimore, Md.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Precision pathophysiology in steatotic liver disease.Clinical and molecular hepatology · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
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  11. Article
  12. Cysteine-rich domain of type III collagen N-propeptide inhibits fibroblast activation by attenuating TGFβ signaling.Matrix biology : journal of the International Society for Matrix Biology · 2022
    Article
  13. Article
  14. International journal of molecular sciences · 2020
    Article
  15. Article
  16. Article
  17. 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

17 authors at 4 institutions in 3 countries.

Cyrielle CaussyNAFLD Research Center, Department of Medicine, University of California at San Diego, La Jolla, CA.
Meera BhargavaNAFLD Research Center, Department of Medicine, University of California at San Diego, La Jolla, CA.
Ida F VillesenDepartment of Biomarkers and Research, Nordic Bioscience, Herlev, Denmark.
Natasja S GudmannDepartment of Biomarkers and Research, Nordic Bioscience, Herlev, Denmark.
Diana J LeemingDepartment of Biomarkers and Research, Nordic Bioscience, Herlev, Denmark.
Morten A KarsdalDepartment of Biomarkers and Research, Nordic Bioscience, Herlev, Denmark.
Claire FaulknerNAFLD Research Center, Department of Medicine, University of California at San Diego, La Jolla, CA.
Denny BaoNAFLD Research Center, Department of Medicine, University of California at San Diego, La Jolla, CA.
Amy LiuNAFLD Research Center, Department of Medicine, University of California at San Diego, La Jolla, CA.
Min-Tzu LoDepartment of Radiology, University of California at San Diego, La Jolla, CA.
Ricki BettencourtNAFLD Research Center, Department of Medicine, University of California at San Diego, La Jolla, CA.
Shirin BassirianNAFLD Research Center, Department of Medicine, University of California at San Diego, La Jolla, CA.
Lisa RichardsNAFLD Research Center, Department of Medicine, University of California at San Diego, La Jolla, CA.
David A BrennerNAFLD Research Center, Department of Medicine, University of California at San Diego, La Jolla, CA.
Chi-Hua ChenDepartment of Radiology, University of California at San Diego, La Jolla, CA.
Claude B SirlinLiver Imaging Group, Department of Radiology, University of California at San Diego, La Jolla, CA.
Rohit LoombaNAFLD Research Center, Department of Medicine, University of California at San Diego, La Jolla, CA.
University of California, San Diego · USNordic Bioscience (Denmark) · DKLa Jolla Alcohol Research · USUniversité Claude Bernard Lyon 1 · FR

Funding

UC San Diego Clinical and Translational Research InstituteUL1TR001442 · NCATS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIRESTEIN, GARY S, HOGARTH, MICHAEL · 2015 to 2024
$88.3M
Yeast Genetics and Stress Response Genes-BiomedicalP42ES010337 · NIEHS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TUKEY, ROBERT H · 2000 to 2022
$69.8M
QUS Technology for Diagnosis and Grading of Hepatic Steatosis in NAFLDR01DK106419 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LOOMBA, ROHIT, SIRLIN, CLAUDE B · 2015 to 2019
$3.4M
GENETIC EPIDEMIOLOGY OF NONALCOHOLIC FATTY LIVER DISEASEK23DK090303 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LOOMBA, ROHIT · 2011 to 2014
$721k
NCATS NIH HHS UL1 TR001442NIDDK NIH HHS K23 DK090303NIDDK NIH HHS R01 DK106419NIEHS NIH HHS P42 ES010337
6 · The paper itself

Abstract

N-terminal propeptide of type 3 procollagen (PRO-C3) is a biomarker of liver fibrosis in nonalcoholic fatty liver disease (NAFLD). This study examines the association between PRO-C3 concentration and liver fibrosis assessed by magnetic resonance elastography (MRE)-measured stiffness (MRE-stiffness) and the heritability of PRO-C3 concentration in a cohort of twins and families with and without NAFLD. We performed a cross-sectional analysis of a well-characterized prospective cohort of 306 participants, including 44 probands with NAFLD-cirrhosis and their 72 first-degree relatives, 24 probands with NAFLD without advanced fibrosis and their 24 first-degree relatives, and 72 controls without NAFLD and their 72 first-degree relatives. Liver steatosis was assessed by magnetic resonance imaging proton density fat fraction, and liver fibrosis was assessed by MRE-stiffness. Serum PRO-C3 was assessed by competitive, enzyme-linked immunosorbent assay. We assessed the familial correlation of PRO-C3 concentration, the shared gene effects between PRO-C3 concentration and liver steatosis and fibrosis, and the association between PRO-C3 concentration and genetic variants in the patatin-like phospholipase domain-containing 3 (PNPLA3), transmembrane 6 superfamily member 2 (TM6SF2), membrane-bound O-acyltransferase domain-containing (MBOAT), and glucokinase regulator (CGKR) genes. In multivariable-adjusted models including age, sex, body mass index, and ethnicity, serum PRO-C3 correlated strongly with liver fibrosis (r

Indexed as

AdultAgedCollagen Type IIIElasticity Imaging TechniquesEpidemiologic StudiesExtracellular MatrixFemaleHumansLiver CirrhosisMaleMembrane ProteinsMiddle AgedNon-alcoholic Fatty Liver DiseaseQuantitative Trait, HeritableCollagen Type IIIMembrane ProteinsTM6SF2 protein, human

Identifiers

PMID30859582
PMCPMC6984974
OpenAlexW2921734144

What OpenQuestion holds

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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.