Evidence map›Paper›PMID 42653422›Full record

ArticleInternational journal of molecular sciences2026

Genetically Determined Loss-of-Function of the Organic Cation Transporter OCT1 Is Associated with Lower Liver Fat Content in Humans.

Anna K Scheurer-Böhme, Eileen Moritz, Stefan Weiss, Robin Bülow, Marie-Luise Kromrey, M Kamal Nasr, Uwe Völker, Henry Völzke, Stefan Engeli, Jens-Peter Kühn and 2 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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

12 authors.

Anna K Scheurer-BöhmeDepartment of General Pharmacology, Institute of Pharmacology, Center of Drug Absorption and Transport (C DAT), University Medicine Greifswald, 17475 Greifswald, Mecklenburg-Western Pomerania, Germany.
Eileen MoritzDepartment of General Pharmacology, Institute of Pharmacology, Center of Drug Absorption and Transport (C DAT), University Medicine Greifswald, 17475 Greifswald, Mecklenburg-Western Pomerania, Germany.
Stefan WeissInterfaculty Institute of Genetics and Functional Genomics, University Medicine Greifswald, 17475 Greifswald, Mecklenburg-Western Pomerania, Germany.ORCID 0000-0002-3553-4315
Robin BülowDZHK (German Centre for Cardiovascular Research), Partner Site North, 17475 Greifswald, Mecklenburg-Western Pomerania, Germany.ORCID 0000-0003-1884-5784
Marie-Luise KromreyInstitute of Diagnostic Radiology and Neuroradiology, University Medicine Greifswald, 17475 Greifswald, Mecklenburg-Western Pomerania, Germany.ORCID 0000-0002-0420-7303
M Kamal NasrDZHK (German Centre for Cardiovascular Research), Partner Site North, 17475 Greifswald, Mecklenburg-Western Pomerania, Germany.ORCID 0009-0004-2816-7168
Uwe VölkerInterfaculty Institute of Genetics and Functional Genomics, University Medicine Greifswald, 17475 Greifswald, Mecklenburg-Western Pomerania, Germany.ORCID 0000-0002-5689-3448
Henry VölzkeInstitute for Community Medicine, University Medicine Greifswald, 17475 Greifswald, Mecklenburg-Western Pomerania, Germany.
Stefan EngeliDepartment of Clinical Pharmacology, Institute of Pharmacology, Center of Drug Absorption and Transport (C DAT), University Medicine Greifswald, 17475 Greifswald, Mecklenburg-Western Pomerania, Germany.
Jens-Peter KühnInstitute and Policlinic for Diagnostic and Interventional Radiology, University Hospital, Carl Gustav Carus University, TU Dresden, 01304 Dresden, Saxony, Germany.
Alexander TeumerDZHK (German Centre for Cardiovascular Research), Partner Site North, 17475 Greifswald, Mecklenburg-Western Pomerania, Germany.ORCID 0000-0002-8309-094X
Mladen V TzvetkovDepartment of General Pharmacology, Institute of Pharmacology, Center of Drug Absorption and Transport (C DAT), University Medicine Greifswald, 17475 Greifswald, Mecklenburg-Western Pomerania, Germany.ORCID 0000-0003-1670-5534

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fatty liver is associated with increased all-cause mortality. Organic cation transporter 1 (OCT1) is a polyspecific hepatic uptake transporter. OCT1 mediates hepatic uptake of vitamin B1 (thiamine); thus, OCT1 deficiency may impair thiamine availability and consequently reduce glucose-derived energy. Consequently, OCT1-knockout mice exhibit significantly reduced liver fat. In 2% of Europeans and White Americans, common genetic variants markedly reduce OCT1 function. In this study, we used these naturally occurring variants to investigate the influences of reduced OCT1 function on liver fat in humans. We analyzed 2512 whole-body MRI datasets from the Study of Health in Pomerania (SHIP) and validated the findings using 31,594 datasets from the UK Biobank. In both cohorts, OCT1 deficiency was associated with lower fat content in the liver (

Indexed as

Fatty LiverLiverOctamer Transcription Factor-1Organic Cation Transporter 1AgedAnimalsFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedOctamer Transcription Factor-1Organic Cation Transporter 1hepatic steatosismetabolic dysfunction-associated steatotic liver diseasemetabolic phenotypemitochondrial respirationnon-alcoholic fatty liver diseaseOCT1organic cation transporterStudy of Health in PomeraniaUK Biobank

Identifiers

PMID42653422
PMCPMC13513528

What Socratic 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 Socratic graph.