Evidence map›Paper›PMID 42688017›Full record

ArticleResearch square2026

A Changing Paradigm: The Swift Expansion of Adult Living Donor Liver Transplantation for MASH Cirrhosis.

Rei Matsumoto, Stephanie Silpe, Maria E Cortes, Alexis Kim, Cheng Han Ng, Anh T Bui, Garren Mongtomery, Brian J Wentworth, Curt K Argo, Nicolas M Intagliata and 9 more

Abstract readPreprint
In one paragraph

Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Rei MatsumotoUniversity of Virginia.
Stephanie SilpeUniversity of Virginia.
Maria E CortesUniversity of Virginia.
Alexis KimVirginia Commonwealth University.
Cheng Han NgNational University, National University Hospital.
Anh T BuiVirginia Commonwealth University.
Garren MongtomeryUniversity of Virginia.
Brian J WentworthUniversity of Virginia.
Curt K ArgoUniversity of Virginia.
Nicolas M IntagliataUniversity of Virginia.
Neeral L ShahUniversity of Virginia.
Stephen H CaldwellUniversity of Virginia.
Anya MezinaUniversity of Virginia.
Yazan Al-AdwanUniversity of Virginia.
Shawn PelletierUniversity of Virginia.
Juan F GuerraUniversity of Virginia.
Anita SitesUniversity of Virginia.
Mohammad S SiddiquiUniversity of Virginia.
Zachary H HenryUniversity of Virginia.

Funding

Predicting outcomes in nonalcoholic steatohepatitis with advanced fibrosisR01DK129564 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI ARUN J SANYAL, Mohammad Shadab Siddiqui · 2022 to 2026
$2.8M
NIDDK NIH HHS R01 DK129564
6 · The paper itself

Abstract

Living donor liver transplantation (LDLT) provides a lifesaving option for patients with end-stage liver disease who may not be prioritized for deceased donor transplantation under the current model for end-stage liver disease (MELD)-based allocation system. Although prior studies have demonstrated a survival benefit for LDLT compared with remaining on the waitlist, limited data account for evolving liver disease epidemiology and donor characteristics in the United States. Methods: Using data from the Scientific Registry of Transplant Recipients/United Network of Organ Sharing (SRTR/UNOS), we conducted a retrospective cohort analysis of adult LDLT recipients and donors from 2000 to 2024. Trends were assessed using descriptive statistics and logistic regression. Results: A total of 7,686 LDLT recipients were identified. Indications included cholestatic liver disease (23%), hepatitis C virus (HCV) infection (16%), metabolic dysfunction-associated steatohepatitis (MASH) (15%), and alcohol-associated liver disease (ALD) (14%). MELD scores at LT varied by etiology, with higher scores in MASH and ALD. From 2000 to 2024, LDLT for MASH increased 5.4-fold (5.6% to 30.2%), while HCV declined sharply after 2014. LDLT for ALD remained stable despite increasing waitlist registrations. MASH recipients were more likely to receive grafts from younger related donors and less likely from older related donors or spouses compared with cholestatic liver disease. Conclusions: MASH is the fastest-growing indication for LDLT in the United States. These findings highlight limitations of MELD-based allocation and suggest a need to address donor eligibility barriers to improve equitable access to transplantation across liver disease etiologies.

Indexed as

alcohol associated liver diseasecirrhosisliver transplantliving donor liver transplantmetabolic dysfunction associated steatohepatitis

Identifiers

PMID42688017
PMCPMC13533020

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.