Cardiovascular disease risk assessment in Japanese adults with hemophilia: Interim results of a multicenter study

Abstract Background Although patients with hemophilia have historically been considered at low risk for cardiovascular disease (CVD), recent studies report increasing CVD incidence in this population. Ischemic heart disease incidence is reported lower in Japanese hemophilia patients (~0.3%) compared to Western populations. On the other hand, a Japanese study also reported that approximately 25% of HIV-positive patients with hemophilia exhibited moderate-to-severe coronary atherosclerosis, suggesting a more complex and unclear clinical picture. There is no significant difference in mortality CVD between patients with hemophilia and the general population. However, in patients with hemophilia, the use of anticoagulant or antiplatelet therapy is complex, high-risk, and costly; therefore, identifying CVD risk factors and implementing preventive strategies is essential. Objective To investigate the prevalence and risk factors for CVD among adult hemophilia patients without chest symptoms and inform preventative strategies. Methods Between April 2022 and March 2025, hemophilia patients aged ≥30 years who attended participating institutions and provided written informed consent underwent coronary computed tomography (CT) scanning. Health-related quality of life was assessed using the SF-36® v2 questionnaire. Vascular inflammation markers, including interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), intercellular adhesion molecule-1 (ICAM-1), and high-sensitivity C-reactive protein (hs-CRP), were measured from blood samples. Pulse wave velocity (PWV) testing was also conducted. An interim analysis was performed on cases for which complete data were available as of June 2025. Univariate analyses were conducted to evaluate the association between individual clinical and laboratory parameters and moderate-to-high CVD risk, as determined by coronary CT findings. Statistical analyses were performed using SPSS software. Categorical and continuous variables were compared using the chi-square test and Mann–Whitney U test, respectively. A p-value of <0.05 was considered statistically significant. Results A total of 126 patients (hemophilia A: 109, hemophilia B: 17) underwent coronary CT. Among those with hemophilia A, 69 (63.3%) were severe, 24 (22.0%) moderate, and 15 (11.9%) mild; 1 had inhibitors. In hemophilia B, 15 (88.2%) were severe and 2 (11.8%) were moderate, with inhibitors in 2 patients. Treatment regimens for hemophilia A included emicizumab (n=26), prophylaxis with extended half-life factor VIII (EHL-FVIII; n=41), prophylaxis with standard half-life FVIII (SHL-FVIII; n=18), and on-demand therapy (n=24). For hemophilia B: prophylaxis with EHL-FIX (n=11), prophylaxis with SHL-FIX (n=1), on-demand therapy (n=3), and regular bypassing agent use (n=2). Median age of all patients was 54.0 years (IQR: 45.0–61.0). Prevalence of CVD risk factors among all patients included hypertension (41.3%), dyslipidemia (28.6%), diabetes (13.5%), chronic kidney disease (12.7%), current smoking (16.7%), and HIV infection (26.2%). Patients were stratified by Agatston score into low-risk (<100; n=97) and moderate-to-high-risk (≥100; n=29) groups. The moderate-to-high-risk group was significantly older and had higher rates of hypertension, dyslipidemia, and diabetes. TNF-α levels and baPWV were significantly elevated in this group. No significant differences were observed in SF-36®v2 scores. All 29 moderate-to-high-risk patients were recommended for cardiology referral; however, only 9 underwent coronary angiography. All of 3 patients underwent coronary angiography in the high-risk subgroup (Agatston ≥400; n=9) showed moderate or greater coronary stenosis; one started antiplatelet therapy. In the moderate-risk subgroup (Agatston 100–399; n=20), 3 of 6 patients received coronary angiography had moderate or greater stenosis, with one requiring coronary artery bypass grafting. Conclusion In this study, the risk of CVD in Japanese patients with hemophilia appeared comparable to that of the general population. Aging, hypertension, dyslipidemia, and diabetes were identified as major risk factors for CVD. Additionally, TNF-α and baPWV emerged as potential markers for identifying individuals at moderate or higher risk of coronary artery disease, warranting further investigation.

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Journal
Blood
Published
2025-11-03
DOI
https://doi.org/10.1182/blood-2025-4843
Primary Topic
Hemophilia Treatment and Research
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article
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article

Cardiovascular disease risk assessment in Japanese adults with hemophilia: Interim results of a multicenter study

Yushi Chikasawa, Ei Kinai, Tsukasa Osaki, Mitsuhiro Ishikura et al.
Blood
Hemophilia Treatment and Research
article

Cardiovascular disease risk assessment in Japanese adults with hemophilia: Interim results of a multicenter study

Yushi Chikasawa, Ei Kinai, Tsukasa Osaki, Mitsuhiro Ishikura, Azusa Nagao, Kagehiro Amano, Hisanori Kosuge, Takashi Muramatsu, Masato Bingo, Akito Ichiki, Ryui Miyashita, Mihoko Yotsumoto, Kazuhiro Satomi, Shun KANEKO, Satoshi Hida, Tomoko Yamaguchi, Takeshi Hagiwara
article en

Abstract

Abstract Background Although patients with hemophilia have historically been considered at low risk for cardiovascular disease (CVD), recent studies report increasing CVD incidence in this population. Ischemic heart disease incidence is reported lower in Japanese hemophilia patients (~0.3%) compared to Western populations. On the other hand, a Japanese study also reported that approximately 25% of HIV-positive patients with hemophilia exhibited moderate-to-severe coronary atherosclerosis, suggesting a more complex and unclear clinical picture. There is no significant difference in mortality CVD between patients with hemophilia and the general population. However, in patients with hemophilia, the use of anticoagulant or antiplatelet therapy is complex, high-risk, and costly; therefore, identifying CVD risk factors and implementing preventive strategies is essential. Objective To investigate the prevalence and risk factors for CVD among adult hemophilia patients without chest symptoms and inform preventative strategies. Methods Between April 2022 and March 2025, hemophilia patients aged ≥30 years who attended participating institutions and provided written informed consent underwent coronary computed tomography (CT) scanning. Health-related quality of life was assessed using the SF-36® v2 questionnaire. Vascular inflammation markers, including interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), intercellular adhesion molecule-1 (ICAM-1), and high-sensitivity C-reactive protein (hs-CRP), were measured from blood samples. Pulse wave velocity (PWV) testing was also conducted. An interim analysis was performed on cases for which complete data were available as of June 2025. Univariate analyses were conducted to evaluate the association between individual clinical and laboratory parameters and moderate-to-high CVD risk, as determined by coronary CT findings. Statistical analyses were performed using SPSS software. Categorical and continuous variables were compared using the chi-square test and Mann–Whitney U test, respectively. A p-value of <0.05 was considered statistically significant. Results A total of 126 patients (hemophilia A: 109, hemophilia B: 17) underwent coronary CT. Among those with hemophilia A, 69 (63.3%) were severe, 24 (22.0%) moderate, and 15 (11.9%) mild; 1 had inhibitors. In hemophilia B, 15 (88.2%) were severe and 2 (11.8%) were moderate, with inhibitors in 2 patients. Treatment regimens for hemophilia A included emicizumab (n=26), prophylaxis with extended half-life factor VIII (EHL-FVIII; n=41), prophylaxis with standard half-life FVIII (SHL-FVIII; n=18), and on-demand therapy (n=24). For hemophilia B: prophylaxis with EHL-FIX (n=11), prophylaxis with SHL-FIX (n=1), on-demand therapy (n=3), and regular bypassing agent use (n=2). Median age of all patients was 54.0 years (IQR: 45.0–61.0). Prevalence of CVD risk factors among all patients included hypertension (41.3%), dyslipidemia (28.6%), diabetes (13.5%), chronic kidney disease (12.7%), current smoking (16.7%), and HIV infection (26.2%). Patients were stratified by Agatston score into low-risk (<100; n=97) and moderate-to-high-risk (≥100; n=29) groups. The moderate-to-high-risk group was significantly older and had higher rates of hypertension, dyslipidemia, and diabetes. TNF-α levels and baPWV were significantly elevated in this group. No significant differences were observed in SF-36®v2 scores. All 29 moderate-to-high-risk patients were recommended for cardiology referral; however, only 9 underwent coronary angiography. All of 3 patients underwent coronary angiography in the high-risk subgroup (Agatston ≥400; n=9) showed moderate or greater coronary stenosis; one started antiplatelet therapy. In the moderate-risk subgroup (Agatston 100–399; n=20), 3 of 6 patients received coronary angiography had moderate or greater stenosis, with one requiring coronary artery bypass grafting. Conclusion In this study, the risk of CVD in Japanese patients with hemophilia appeared comparable to that of the general population. Aging, hypertension, dyslipidemia, and diabetes were identified as major risk factors for CVD. Additionally, TNF-α and baPWV emerged as potential markers for identifying individuals at moderate or higher risk of coronary artery disease, warranting further investigation.

BloodVol. 146(Supplement 1)
Tokyo Medical University (JP), Ogikubo Hospital (JP), Osaka International Cancer Institute (JP)
Openalex Percentile: Top 45%
Hemophilia Treatment and Research
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