Evidence map›Paper›PMID 38951512›Full record

ArticleNature communications2024

Distinct genetic liability profiles define clinically relevant patient strata across common diseases.

Lucia Trastulla, Georgii Dolgalev, Sylvain Moser, Laura T Jiménez-Barrón, Till F M Andlauer, Moritz von Scheidt, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Monika Budde, Urs Heilbronner, Sergi Papiol and 11 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Lucia TrastullaMax Planck Institute of Psychiatry, Munich, Germany.ORCID 0000-0001-8749-475X
Georgii DolgalevDepartment of Psychiatry, University of Münster, Münster, Germany.
Sylvain MoserMax Planck Institute of Psychiatry, Munich, Germany.
Laura T Jiménez-BarrónMax Planck Institute of Psychiatry, Munich, Germany.
Till F M AndlauerMax Planck Institute of Psychiatry, Munich, Germany.ORCID 0000-0002-2917-5889
Moritz von ScheidtKlinik für Herz-und Kreislauferkrankungen, Deutsches Herzzentrum München, Technical University Munich, Munich, Germany.
Schizophrenia Working Group of the Psychiatric Genomics Consortium
Monika BuddeInstitute of Psychiatric Phenomics and Genomics (IPPG), LMU University Hospital, LMU Munich, Munich, 80336, Germany.
Urs HeilbronnerInstitute of Psychiatric Phenomics and Genomics (IPPG), LMU University Hospital, LMU Munich, Munich, 80336, Germany.ORCID 0000-0001-7135-762X
Sergi PapiolMax Planck Institute of Psychiatry, Munich, Germany.ORCID 0000-0001-9366-8728
Alexander TeumerGerman Center for Cardiovascular Research (DZHK), Partner Site Greifswald, Greifswald, Germany.ORCID 0000-0002-8309-094X
Georg HomuthInterfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.
Henry VölzkeGerman Center for Cardiovascular Research (DZHK), Partner Site Greifswald, Greifswald, Germany.
Marcus DörrGerman Center for Cardiovascular Research (DZHK), Partner Site Greifswald, Greifswald, Germany.ORCID 0000-0001-7471-475X
Peter FalkaiMax Planck Institute of Psychiatry, Munich, Germany.ORCID 0000-0002-0284-2290
Thomas G SchulzeInstitute of Psychiatric Phenomics and Genomics (IPPG), LMU University Hospital, LMU Munich, Munich, 80336, Germany.
Julien GagneurSchool of Computation, Information and Technology, Technical University of Munich, Garching, Germany.ORCID 0000-0002-8924-8365
Francesco IorioHuman Technopole, Milan, Italy.ORCID 0000-0001-7063-8913
Bertram Müller-MyhsokMax Planck Institute of Psychiatry, Munich, Germany.ORCID 0000-0002-0719-101X
Heribert SchunkertKlinik für Herz-und Kreislauferkrankungen, Deutsches Herzzentrum München, Technical University Munich, Munich, Germany.ORCID 0000-0001-6428-3001
Michael J ZillerMax Planck Institute of Psychiatry, Munich, Germany. ziller@uni-muenster.de.ORCID 0000-0003-0781-7980

Funding

VESICULAR LOCALIZATION AND FUNCTION OF PRESENILIN 1 FRAGMENTP50AG005138 · NIA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI SCHIMMING, CORBETT · 1985 to 2019
$37.9M
QUANTITATIVE ANALYSIS OF MICROVASCULAR CHANGES IN THE AGING BRAINP01AG002219 · NIA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI HAROUTUNIAN, VAHRAM · 1985 to 2009
$19.2M
White Matter Abnormalities in SchizophreniaP50MH066392 · NIMH · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI BUXBAUM, JOSEPH D. · 2002 to 2012
$18.6M
Project 5: In vivo measurement of GABA transmission in healthy controls & subjectP50MH084053 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LEWIS, DAVID A · 2008 to 2012
$11.5M
International Cohort Collection for Bipolar DisorderR01MH085542 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI SMOLLER, JORDAN W · 2008 to 2012
$10.7M
Cis-Regulatory Epigenome Mappings in SchizophreniaU01MH103392 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI AKBARIAN, SCHAHRAM, SKLAR, PAMELA · 2014 to 2017
$7.6M
Molecular Profiling of SchizophreniaR01MH110921 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHESS, ANDREW J, ROUSSOS, PANAGIOTIS · 2016 to 2020
$6.9M
Genetics Association in Schizophrenia and Other DisordersR37MH057881 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DEVLIN, BERNIE · 2013 to 2022
$5.4M
Risk genetic variants and cis regulation of gene expression in Bipolar DisorderR01MH109677 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ROUSSOS, PANAGIOTIS · 2016 to 2020
$4.6M
Deciphering the molecular basis of T1D in human cells using functional genomicsDP3DK111898 · NIDDK · HARVARD UNIVERSITY · PI CARR, STEVEN A, MAEHR, RENE · 2016 to 2016
$4.2M
Src mediates molecular alterations leading to NMDAR hypofunction in schizophreniaR01MH075916 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BORGMANN-WINTER, KARIN, HAHN, CHANG-GYU · 2006 to 2019
$3.3M
Integrated Multiscale Networks in SchizophreniaR01MH109897 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BRENNAND, KRISTEN JENNIFER, ROUSSOS, PANAGIOTIS · 2016 to 2020
$3.0M
Brain and Behavior Research Foundation (Brain & Behavior Research Foundation) NARSAD Young Investigator GrantBritish Heart Foundation (BHF) 81X2600522Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 01EE1404HBundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 01EW 2005Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 01EW 2009Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 01ZX1504Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 01ZX1614KBundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 01ZX1706Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 01ZX1904ABundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 031L0174ABundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 031L0174BBundesministerium für Wirtschaft und Energie (Federal Ministry for Economic Affairs and Energy) ZF4590201BA8Deutsche Forschungsgemeinschaft (German Research Foundation) SCHU 1603/4-1, 5-1, 7-1; FA241/16-1Deutsche Forschungsgemeinschaft (German Research Foundation) SFB 1123 (B02)Deutsche Forschungsgemeinschaft (German Research Foundation) SFB TRR 267 (B05).NIA NIH HHS P01 AG002219NIA NIH HHS P50 AG005138NIDA NIH HHS HHSN271201300031CNIDDK NIH HHS DP3 DK111898NIMH NIH HHS P50 MH066392NIMH NIH HHS P50 MH084053NIMH NIH HHS R01 MH075916NIMH NIH HHS R01 MH080405NIMH NIH HHS R01 MH085542NIMH NIH HHS R01 MH093725NIMH NIH HHS R01 MH097276NIMH NIH HHS R01 MH109677NIMH NIH HHS R01 MH109897NIMH NIH HHS R01 MH110921NIMH NIH HHS R01 MH124873NIMH NIH HHS R37 MH057881NIMH NIH HHS U01 MH103392
6 · The paper itself

Abstract

Stratified medicine holds great promise to tailor treatment to the needs of individual patients. While genetics holds great potential to aid patient stratification, it remains a major challenge to operationalize complex genetic risk factor profiles to deconstruct clinical heterogeneity. Contemporary approaches to this problem rely on polygenic risk scores (PRS), which provide only limited clinical utility and lack a clear biological foundation. To overcome these limitations, we develop the CASTom-iGEx approach to stratify individuals based on the aggregated impact of their genetic risk factor profiles on tissue specific gene expression levels. The paradigmatic application of this approach to coronary artery disease or schizophrenia patient cohorts identified diverse strata or biotypes. These biotypes are characterized by distinct endophenotype profiles as well as clinical parameters and are fundamentally distinct from PRS based groupings. In stark contrast to the latter, the CASTom-iGEx strategy discovers biologically meaningful and clinically actionable patient subgroups, where complex genetic liabilities are not randomly distributed across individuals but rather converge onto distinct disease relevant biological processes. These results support the notion of different patient biotypes characterized by partially distinct pathomechanisms. Thus, the universally applicable approach presented here has the potential to constitute an important component of future personalized medicine paradigms.

Indexed as

Coronary Artery DiseaseGenetic Predisposition to DiseaseMultifactorial InheritanceSchizophreniaFemaleGenome-Wide Association StudyHumansMaleMiddle AgedPolymorphism, Single NucleotidePrecision MedicineRisk Factors

Identifiers

PMID38951512
PMCPMC11217418

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