Protocol of the Berlin Long-term Observation of Vascular Events (BeLOVE): a prospective cohort study with deep phenotyping and long-term follow up of cardiovascular high-risk patients

Author:

Weber Joachim EORCID,Ahmadi MichaelORCID,Boldt Leif-HendrikORCID,Eckardt Kai-UweORCID,Edelmann FrankORCID,Gerhardt HolgerORCID,Grittner UlrikeORCID,Haubold KathrinORCID,Hübner NorbertORCID,Kollmus-Heege JilORCID,Landmesser UlfORCID,Leistner David MORCID,Mai KnutORCID,Müller Dominik NORCID,Nolte Christian HORCID,Pieske BurkertORCID,Piper Sophie KORCID,Rattan SimritORCID,Rauch GeraldineORCID,Schmidt SeinORCID,Schmidt-Ott Kai MORCID,Schönrath KatharinaORCID,Schulz-Menger JeanetteORCID,Schweizerhof OliverORCID,Siegerink BobORCID,Spranger JoachimORCID,Ramachandran Vasan SORCID,Witzenrath MartinORCID,Endres MatthiasORCID,Pischon TobiasORCID

Abstract

IntroductionThe Berlin Long-term Observation of Vascular Events is a prospective cohort study that aims to improve prediction and disease-overarching mechanistic understanding of cardiovascular (CV) disease progression by comprehensively investigating a high-risk patient population with different organ manifestations.Methods and analysisA total of 8000 adult patients will be recruited who have either suffered an acute CV event (CVE) requiring hospitalisation or who have not experienced a recent acute CVE but are at high CV risk. An initial study examination is performed during the acute treatment phase of the index CVE or after inclusion into the chronic high risk arm. Deep phenotyping is then performed after ~90 days and includes assessments of the patient’s medical history, health status and behaviour, cardiovascular, nutritional, metabolic, and anthropometric parameters, and patient-related outcome measures. Biospecimens are collected for analyses including ‘OMICs’ technologies (e.g., genomics, metabolomics, proteomics). Subcohorts undergo MRI of the brain, heart, lung and kidney, as well as more comprehensive metabolic, neurological and CV examinations. All participants are followed up for up to 10 years to assess clinical outcomes, primarily major adverse CVEs and patient-reported (value-based) outcomes. State-of-the-art clinical research methods, as well as emerging techniques from systems medicine and artificial intelligence, will be used to identify associations between patient characteristics, longitudinal changes and outcomes.Ethics and disseminationThe study was approved by the Charité—Universitätsmedizin Berlin ethics committee (EA1/066/17). The results of the study will be disseminated through international peer-reviewed publications and congress presentations.Study registrationFirst study phase: Approved WHO primary register: German Clinical Trials Register:https://drks.de/search/de/trial/DRKS00016852; WHO International Clinical Registry Platform:http://apps.who.int/trialsearch/Trial2.aspx?TrialID=DRKS00016852. Recruitment started on July 18, 2017.Second study phase: Approved WHO primary register: German Clinical Trials Register DRKS00023323, date of registration: November 4, 2020, URL:http://www.drks.de/DRKS00023323. Recruitment started on January 1, 2021.

Funder

Berlin Institute of Health

Publisher

BMJ

Subject

General Medicine

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