Evidence map›Paper›PMID 42404081›Full record

ArticleBMJ neurology open2026

Stroke and its consequences: protocol and pilot data of the observational Berlin Long-term Observation of Vascular Events (BeLOVE) stroke stratum.

Christian H Nolte, Joachim E Weber, Michael Ahmadi, Leif-Hendrik Boldt, Tim B Braemswig, Frederik Damm, Jakob I Doerrfuss, Kai-Uwe Eckardt, Frank Edelmann, Ivana Galinovic and 27 more

Abstract read
In one paragraph

Article in BMJ neurology open, 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

37 authors.

Christian H NolteDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0001-5577-1775
Joachim E WeberBIH, Berlin, Germany.
Michael AhmadiBIH, Berlin, Germany.
Leif-Hendrik BoldtDHZC, Berlin, BE, Germany.
Tim B BraemswigDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Frederik DammBIH, Berlin, Germany.
Jakob I DoerrfussCharité - Universitätsmedizin Berlin, Berlin, Germany.
Kai-Uwe EckardtDepartment of Nephrology and Medical Intensive Care, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Frank EdelmannDHZC, Berlin, BE, Germany.
Ivana GalinovicCharité University Hospital Berlin Center for Stroke Research Berlin, Berlin, Germany.
Holger GerhardtBIH, Berlin, Germany.
Ulrike GrittnerCharité University Hospital Berlin Institute of Biometry and Clinical Epidemiology, Berlin, Germany.
Norbert HübnerMax Delbruck Centre for Molecular Medicine in the Helmholtz Association, Buch, BE, Germany.
Jil HeegeCharité University Hospital Berlin Institute of Biometry and Clinical Epidemiology, Berlin, Germany.
Anna KufnerDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Thomas LimanDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Andreas MeiselDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Dominik N MüllerMax-Delbrück-Centrum für Molekulare Medizin in der Helmholtz-Gemeinschaft, Buch, Germany.
Christian OtteCharité University Hospital Berlin Center for Stroke Research Berlin, Berlin, Germany.
Rafaela M PintoBIH, Berlin, Germany.
Sophie PiperCharité University Hospital Berlin Institute of Biometry and Clinical Epidemiology, Berlin, Germany.
Simrit RattanCharité University Hospital Berlin Institute of Biometry and Clinical Epidemiology, Berlin, Germany.
Regina I von RennenbergDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Ira Rohrpasser-NapierkowskiBIH, Berlin, Germany.
Jan F ScheitzDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Katharina SchoenrathBIH, Berlin, Germany.
Jeanette Schulz-MengerMax Delbruck Centre for Molecular Medicine in the Helmholtz Association, Buch, BE, Germany.
Oliver SchweizerhofBIH, Berlin, Germany.ORCID https://orcid.org/0000-0002-8954-4818
Pia S SperberBIH, Berlin, Germany.
Lena Steindorf-SabathDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Alina StegemannDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0003-0401-0698
Helena StenglDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Kersten VillringerCharité University Hospital Berlin Center for Stroke Research Berlin, Berlin, Germany.
Ulf LandmesserBIH, Berlin, Germany.
Knut MaiDepartment of Endocrinology and Metabolism; European Reference Network on Rare Endocrine Diseases (ENDO-ERN), Charité - Universitätsmedizin Berlin, Berlin, Germany.
Tobias PischonMax Delbruck Centre for Molecular Medicine in the Helmholtz Association, Buch, BE, Germany.
Matthias EndresDepartment of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Following a cerebrovascular event, the associated risks for further major adverse cerebro- and cardiovascular events and death (MACE) and important aspects of cognitive, mental and patient-reported outcomes are currently not understood, particularly long-term. Here, we present the study design of the ongoing Berlin Long-term Observation of Vascular Events (BeLOVE) stroke stratum and report data of the first study phase. Methods and analysis: BeLOVE is a prospective, longitudinal, observational, hospital-based cohort study. Its stroke stratum enrols adult patients with acute ischaemic stroke, transient ischaemic attack (TIA) or non-traumatic intracerebral haemorrhage. Patients undergo deep phenotyping including cerebral and cardiac MRI, ECG, echocardiography and bio-sampling including multi-omics analyses. Regular, standardised follow-ups take place annually over a period of up to 10 years and record the frequency of MACE as the primary outcome.Secondary outcomes include the frequency, progression and interactions of functional impairments, namely post-stroke cognition, pain, depression, seizures and their relationship to quality of life.The first study phase included 758 patients (median 69 years, 37% female). At 2-year follow-up, the cumulative incidence (95% CI) of the composite primary endpoint MACE was 0.107 (0.085 to 0.132) and that of first ischaemic stroke, first myocardial infarction and death were 0.066 (0.049 to 0.086), 0.015 (0.008 to 0.026) and 0.040 (0.027 to 0.056), respectively. Ethics and dissemination: Each participant will provide informed written consent during the acute in-hospital phase. Data will be available for research purposes via a written request to the data use and access committee. Trial registration number: German Clinical Trials Register: http://www.drks.de/DRKS00023323 on 4 November 2020.

Indexed as

COGNITIONEPILEPSYPAINSTROKE

Identifiers

PMID42404081
PMCPMC13330884

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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.