Evidence map›Paper›PMID 29058696›Full record

ArticleBone marrow transplantation2018

Donor and recipient plasma follistatin levels are associated with acute GvHD in Blood and Marrow Transplant Clinical Trials Network 0402.

L M Turcotte, T E DeFor, L F Newell, C S Cutler, M R Verneris, J Wu, A Howard, M L MacMillan, J H Antin, G M Vercellotti and 5 more

Open access · greenAbstract read
In one paragraph

Article in Bone marrow transplantation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. 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

15 authors at 6 institutions in 1 country.

L M TurcotteDivision of Pediatric Hematology/Oncology, University of Minnesota, Minneapolis, MN, USA.
T E DeForBlood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN, USA.
L F NewellCenter for Hematologic Malignancies, Oregon Health & Science University, Portland, OR, USA.
C S CutlerHematologic Malignancy Program, Dana Farber Cancer Institute, Boston, MA, USA.
M R VernerisPediatric BMT and Cell Therapy, University of Colorado Anschutz Medical Campus and Children's Hospital, Denver, CO, USA.
J WuThe EMMES Corporation, Rockville, MD, USA.
A HowardCenter for International Blood and Marrow Transplant Research, Minneapolis, MN, USA.
M L MacMillanBlood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN, USA.
J H AntinHematologic Malignancy Program, Dana Farber Cancer Institute, Boston, MA, USA.
G M VercellottiBlood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN, USA.
Ane SlungaardBlood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN, USA.
B R BlazarBlood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN, USA.
D J WeisdorfBlood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN, USA.
A Panoskaltsis-MortariBlood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN, USA.
S G HoltanBlood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN, USA.
University of Minnesota · USDana-Farber Cancer Institute · USEmmes (United States) · USNational Marrow Donor Program · USOregon Health & Science University · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
Blood and Marrow Transplant Clinical Trials Network DCC- The Medical College of Wisconsin, Inc.U24HL138660 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI Steven M. DeVine, Mehdi Hussain Hamadani · 2017 to 2026
$71.4M
Easy-to-read Informed Consent for HCT Clinical TrialsU10HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2011 to 2016
$43.8M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR002494 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, WEISDORF, DANIEL J · 2018 to 2022
$34.9M
In Vivo Prevention of Murine GVHDR37AI034495 · NIAID · UNIVERSITY OF MINNESOTA · PI Bruce R Blazar · 2017 to 2026
$5.4M
City of Hope Core Clinical Center for the Blood and Marrow Transplant Clinical Trials NetworkUG1HL069278 · NHLBI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI RYOTARO NAKAMURA · 2017 to 2026
$2.2M
BMT CTN Core - Dana-Farber Cancer Institute and MGH ConsortiumUG1HL069249 · NHLBI · DANA-FARBER CANCER INST · PI Mahasweta Gooptu · 2017 to 2026
$2.2M
BMT CTN Core - University of MinnesotaUG1HL069290 · NHLBI · UNIVERSITY OF MINNESOTA · PI Mark Juckett, Margaret L MacMillan · 2017 to 2026
$1.9M
Infectious Events in Pregnancy: PlGF Contributes to Maternal MorbidityK23HD091369 · NICHD · OREGON HEALTH & SCIENCE UNIVERSITY · PI NEWELL, LAURA F · 2017 to 2020
$634k
NCATS NIH HHS UL1 TR002494NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294NHLBI NIH HHS U24 HL138660NHLBI NIH HHS UG1 HL069249NHLBI NIH HHS UG1 HL069278NHLBI NIH HHS UG1 HL069290NIAID NIH HHS R37 AI034495NICHD NIH HHS K23 HD091369
6 · The paper itself

Abstract

Follistatin is an angiogenic factor elevated in the circulation after allogeneic hematopoietic cell transplantation (HCT). Elevations in follistatin plasma concentrations are associated with the onset of and poor survival after acute GvHD (aGvHD). Using data from the Blood and Marrow Transplant Clinical Trials Network 0402 study (n=247), we sought to further quantify the longitudinal associations between plasma follistatin levels in transplant recipients, as well as baseline HCT donor follistatin levels, and allogeneic HCT outcomes. Higher recipient baseline follistatin levels were predictive of development of aGvHD (P=0.04). High donor follistatin levels were also associated with the incidence of aGvHD (P<0.01). Elevated follistatin levels on day 28 were associated with the onset of grade II-IV aGvHD before day 28, higher 1-year non-relapse mortality (NRM) and lower overall survival. In multivariate analyses, individuals with follistatin levels >1088 pg/mL at day 28 had a 4-fold increased risk for NRM (relative risk (RR)=4.3, 95% confidence interval (CI) 1.9-9.9, P<0.01) and a nearly three-fold increased overall risk for mortality (RR=2.8, 95% CI 1.5-5.2, P<0.01). Given the multiple roles of follistatin in tissue inflammation and repair, and the confirmation that this biomarker is predictive of important HCT outcomes, the pathobiology of these relationships need further study.

Indexed as

Acute DiseaseAdolescentAdultChildFemaleFollistatinGraft vs Host DiseaseHumansMaleMiddle AgedTissue DonorsYoung AdultFollistatin

Identifiers

PMID29058696
PMCPMC5752567
OpenAlexW2766122872

What OpenQuestion holds

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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.