# ABO Blood Groups, Lipids, and Coronary CT Imaging in A Japanese Single-Center Cohort

**Authors:** Hiroyuki Tokue, Azusa Tokue, Yoshito Tsushima

PMC · DOI: 10.3390/medsci14010121 · 2026-03-04

## TL;DR

This study found that ABO blood type does not significantly affect coronary artery disease risk in Japanese adults when considering standard risk factors.

## Contribution

The study provides new evidence on ABO blood groups and coronary disease in a Japanese population using CT imaging.

## Key findings

- ABO blood type was not independently linked to coronary calcium or stenosis after adjusting for standard risk factors.
- Type O blood was associated with lower HDL-C and higher diastolic pressure, but not with coronary disease outcomes.
- Age, sex, hypertension, and diabetes were the main predictors of coronary disease in this cohort.

## Abstract

Background and Objectives: Non-O ABO blood groups have been linked to higher coronary risk, plausibly via hemostatic and lipid pathways. However, evidence in Japanese populations and imaging-defined disease is limited. We examined whether ABO status relates to serum lipids and coronary CT imaging findings in Japanese adults. Materials and Methods: We reviewed adults who underwent coronary CT angiography (CCTA) at our institution. After prespecified exclusions, 865 patients comprised the imaging cohort. For lipid analyses, we excluded patients receiving lipid-lowering therapy at the time of blood sampling, leaving 636 patients (lipid subset). ABO blood group was obtained from the medical record as recorded at registration (patient-reported) and was not re-confirmed by laboratory testing for this study. Outcomes were any coronary artery calcium (Agatston score > 0) and ≥50% luminal stenosis on CCTA. Results: In the lipid subset (n = 636), coronary calcium was present in 44–54% of patients across the four ABO groups and did not differ across groups (p = 0.33). Among assessable scans in the imaging cohort, ≥50% stenosis did not differ across the four ABO groups. In multivariable models (n = 636), older age, male sex, hypertension, and diabetes were independently associated with both outcomes (CAC presence and ≥50% stenosis) (all p < 0.05). For ≥50% stenosis, higher High-Density Lipoprotein-cholesterol (HDL-C) was additionally associated with lower odds (p < 0.05). ABO status (O vs. non-O) was not independently associated with either outcome. Conclusions: In Japanese adults undergoing CCTA, type O blood was tied to lower HDL-C and higher diastolic pressure—features that track with cardiometabolic risk—yet ABO type did not independently relate to coronary calcium or CT-defined stenosis once standard risk factors were considered. These data suggest that, in this setting, ABO adds little beyond conventional risk profiling.

## Linked entities

- **Diseases:** coronary artery disease (MONDO:0005010), diabetes (MONDO:0005015)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** F8 (coagulation factor VIII) [NCBI Gene 2157] {aka AHF, DXS1253E, F8B, F8C, FVIII, HEMA}, VWF (von Willebrand factor) [NCBI Gene 7450] {aka F8VWF, VWD}, ABO (ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase) [NCBI Gene 28] {aka A3GALNT, A3GALT1, GTA, GTB, NAGAT}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}
- **Diseases:** CAC (MESH:D003324), diastolic blood pressure (MESH:D006337), atherosclerosis (MESH:D050197), venous thrombosis (MESH:D020246), venous thromboembolism (MESH:D054556), Diabetes mellitus (MESH:D003920), coronary calcification (MESH:D003323), plaque (MESH:D003773), cardiovascular disease (MESH:D002318), Stenosis (MESH:D003251), DBP (OMIM:261515), injury to (MESH:D014947), Dyslipidemia (MESH:D050171), thrombotic (MESH:D013927), inflammation (MESH:D007249), Chronic kidney disease (MESH:D051436), ischemic heart disease (MESH:D017202), Hypertension (MESH:D006973), calcification (MESH:D002114), artery calcium (MESH:D002128), cancer (MESH:D009369), aortic aneurysm or dissection (MESH:D000784), coronary disease (MESH:D003327), Coronary stenosis (MESH:D023921), metabolic disorders (MESH:D008659), myocardial infarction (MESH:D009203), CKD (MESH:D012080)
- **Chemicals:** glycan (MESH:D011134), Lipid (MESH:D008055), triglycerides (MESH:D014280), O (MESH:D010100), bisoprolol (MESH:D017298), Lp(a) (MESH:D010649), cholesterol (MESH:D002784), CAC (-), TG (MESH:D013866), Calcium (MESH:D002118), glucose (MESH:D005947), landiolol (MESH:C077049), metal (MESH:D008670), propranolol (MESH:D011433), iopamidol (MESH:D007479), creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC13027437