Haemophilia and cardiovascular disease in Japan: Low incidence rates from ADVANCE Japan baseline data

Author:

Nagao Azusa1ORCID,Chikasawa Yushi2ORCID,Sawada Akihiro3,Kanematsu Takeshi4,Yamasaki Naoya5,Takedani Hideyuki6,Nojima Masanori7,Fujii Teruhisa5ORCID,Suzuki Nobuaki8ORCID,Matsushita Tadashi8,Higasa Satoshi3,Amano Kagehiro2,

Affiliation:

1. Department of Blood Coagulation Ogikubo Hospital Tokyo Japan

2. Department of Laboratory Medicine Tokyo Medical University Tokyo Japan

3. Department of Respiratory Medicine and Hematology Hyogo Medical University Hyogo Japan

4. Department of Clinical Laboratory Nagoya University Hospital Aichi Japan

5. Division of Transfusion Medicine Hiroshima University Hospital Hiroshima Japan

6. National Hospital Organization Tsuruga Medical Center Department of Physiotherapy Fukui Japan

7. Center for Translational Research The Institute of Medical Science Hospital The University of Tokyo Tokyo Japan

8. Department of Transfusion Medicine Nagoya University Hospital Aichi Japan

Abstract

AbstractIntroductionWith the increasing life expectancy of people with haemophilia, the risk of cardiovascular disease (CVD) and thrombotic events has become a growing concern. Longitudinal studies on the incidence and risk factors of CVD in this population are limited, and optimal prevention and treatment strategies are yet to be established.AimThis study aimed to present the baseline data of a prospective longitudinal study focusing on a subset of Japanese patients with haemophilia, specifically investigated the incidence, risk factors and treatment modalities for CVD and thrombotic diseases in people aged 40 years in Japan over 10 years through the ADVANCE Japan study.MethodsThe ADVANCE Japan study is a prospective multicentre cohort study involving 600 adult individuals with haemophilia A/B aged 40 years in Japan. The primary endpoint was the incidence of CVD, with secondary endpoints encompassing anticoagulant use, mortality rates, and comparison with the general population.ResultsBaseline data from the 600 participants revealed that thrombotic events occurred in 13 individuals (2.2%), mostly in those with haemophilia A. Atrial fibrillation was observed in 11 participants (1.8%). Hypertension and dyslipidaemia were identified as the prevalent risk factors. Various prophylactic treatments were employed, and no severe bleeding events were observed during the study period.ConclusionThis study provides vital baseline data for a 10‐year prospective investigation of CVD and thrombotic disease risk in people with haemophilia. These findings will contribute to refining prevention and treatment approaches and improving patients’ quality of life.

Funder

Bayer Yakuhin

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

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