Evidence map›Paper›PMID 41696918›Full record

ArticleClinical and translational gastroenterology2026

Alpha-1 Antitrypsin Deficiency in Patients With Cirrhosis in a US National Cohort.

Binu V John, Dustin Bastaich, Andres Samos, Austen Hentschel, Sunny Sandhu, Raphaella D Ferreira, Tamar Taddei, Brian Garnet, David E Kaplan, Michael Campos and 1 more

Abstract read
In one paragraph

Article in Clinical and translational gastroenterology, 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

11 authors.

Binu V JohnDivision of Gastroenterology and Hepatology, Miami VA Medical System, Miami, Florida, USA.
Dustin BastaichDivision of Gastroenterology and Hepatology, Miami VA Medical System, Miami, Florida, USA.
Andres SamosDivision of Gastroenterology and Hepatology, Miami VA Medical System, Miami, Florida, USA.
Austen HentschelDivision of Gastroenterology and Hepatology, Miami VA Medical System, Miami, Florida, USA.
Sunny SandhuDivision of Gastroenterology and Hepatology, Miami VA Medical System, Miami, Florida, USA.
Raphaella D FerreiraDivision of Gastroenterology and Hepatology, Miami VA Medical System, Miami, Florida, USA.
Tamar TaddeiSection of Digestive Diseases, Yale School of Medicine, New Haven, Connecticut, USA.
Brian GarnetDivision of Pulmonary and Critical Care, Miami VA Medical System, Miami, Florida, USA.
David E KaplanDivision of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Michael CamposDivision of Pulmonary and Critical Care, Miami VA Medical System, Miami, Florida, USA.
Bassam DahmanDivision of Gastroenterology and Hepatology, Miami VA Medical System, Miami, Florida, USA.

Funding

CSRD VA I01 CX002654
6 · The paper itself

Abstract

introductionAlpha-1 antitrypsin deficiency (AATD) is a genetic condition that increases susceptibility to chronic lung and liver diseases. There are limited data on testing rates in patients with cirrhosis. Guidelines recommend AATD testing in cryptogenic liver disease but not in patients with an established etiology. We aimed to quantify AATD testing patterns in a national cohort of patients with cirrhosis to inform guidelines.

methodsIn this retrospective cohort study of veterans with a new diagnosis of cirrhosis between January 1, 2008 and January 31, 2020, with follow-up until February 23, 2023, we identified predictors of testing, and of severe AATD (alpha-1 antitrypsin [AAT] < 57 mg/dL or PiSZ/PiZZ phenotype/genotype).

resultsOf the 126,210 patients with cirrhosis, 42,403 (33.6%) were tested, including 38,189 (30.3%) for AAT levels only, 1,103 (0.8%) for genotype/phenotype only, and 3,011 (2.4%) for both. Factors associated with higher AATD testing included specialist evaluation and White race, whereas patients with chronic obstructive pulmonary disease, hepatitis B/C, hepatocellular carcinoma, and hepatic decompensation were less likely to be tested. Only half of the patients with AAT levels of <57 mg/dL underwent genotype/phenotype testing. Most patients (94.7%) with severe AATD-associated liver disease also had an alternate etiology of liver disease, including metabolic dysfunction associated with steatotic liver disease (53.6%) or viral hepatitis (16.1%), and would be missed if testing only patients with cryptogenic liver disease. DISCUSSION: AATD testing rates in veterans with cirrhosis are low, and patients at high-risk are less likely to be tested. Guidelines are needed to emphasize universal AATD testing in patients with cirrhosis regardless of the presence of other risk factors.

Indexed as

alpha 1-Antitrypsinalpha 1-Antitrypsin DeficiencyLiver CirrhosisAgedFemaleGenotypeHumansMaleMiddle AgedPhenotypePractice Guidelines as TopicRetrospective StudiesUnited Statesalpha 1-Antitrypsinalpha 1-antitrypsin deficiencyalpha-1 antitrypsin deficiency related liver diseasechronic liver diseasecirrhosisgenotypephenotype

Identifiers

PMID41696918
PMCPMC13102426

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.