Evidence map›Paper›PMID 38965603›Full record

Observational studyLipids in health and disease2024

Non-O blood types are associated with a greater risk of large artery atherosclerosis stroke and dysregulation of cholesterol metabolism: an observational study.

Lan Gou, Haowen Li, Yingyu Jiang, Yang Liu, Hongqiu Gu, Zhe Xu, Weina Jin, Lanxin Li, Yanfeng Shi, Jie Zhang and 6 more

Abstract readObservational Study
In one paragraph

Observational study in Lipids in health and disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

16 authors.

Lan Gou *Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Haowen Li *China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Yingyu JiangChina National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Yang LiuDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Hongqiu GuChina National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Zhe XuDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Weina JinChina National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Lanxin LiDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Yanfeng ShiDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Jie ZhangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Zhenjuan FangChangping Laboratory, Beijing, China.
Xia MengDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Yong JiangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Hao LiDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Yongjun WangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China. yongjunwang@ncrcnd.org.cn.
Si ChengDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China. sicheng@ncrcnd.org.cn.

Funding

the Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences 2019-I2M-5-029the National Key R&D Program 2022YFC2502400the National Key R&D Program 2022YFE0209600the National Natural Science Foundation of China 82101359the Young Elite Scientists Sponsorship Program by CAST 2023QNRC001
6 · The paper itself

Abstract

backgroundPrevious research on ABO blood types and stroke has been controversial, predominantly suggesting heightened risk of stroke in non-O blood types. Nonetheless, investigations into the correlation and underlying mechanisms between ABO blood groups and stroke subtypes, especially within Chinese cohorts, remain limited.

methodsThe ABO blood types of 9,542 ischaemic stroke (IS) patients were inferred using two ABO gene loci (c.261G > del; c.802G > A). The healthy population was derived from the 1000 Genomes Project. Patients were classified by the causative classification system (CCS). Volcano plot and gene ontology (GO) analysis were employed to explore protein differential expression among blood types. Additionally, HT29 and SW480 cell lines with downregulated ABO expression were generated to evaluate its impact on cholesterol uptake and efflux.

resultsA greater proportion of stroke patients had non-O blood types (70.46%) than did healthy individuals (61.54%). Notable differences in blood type distributions were observed among stroke subtypes, with non-O blood type patients mainly classified as having large artery atherosclerosis (LAA). Clinical baseline characteristics, such as the low-density lipoprotein cholesterol level, activated partial thromboplastin time and thrombin time, varied significantly among blood types. A volcano plot revealed 17 upregulated and 42 downregulated proteins in the O blood type. GO term analysis indicated that downregulated proteins were primarily associated with lipid metabolism pathways. In vitro experiments revealed that reducing ABO gene expression decreased cholesterol uptake and increased cholesterol efflux.

conclusionsThis study revealed that the non-O blood type increased the risk of LAA stroke through cholesterol metabolism.

Indexed as

ABO Blood-Group SystemAtherosclerosisCholesterolStrokeAgedCholesterol, LDLFemaleHT29 CellsHumansMaleMiddle AgedRisk FactorsABO Blood-Group SystemCholesterolCholesterol, LDLABO blood typeCholesterol uptake and effluxIschaemic strokeLarge artery atherosclerosisNon-O blood typeStroke subtype

Identifiers

PMID38965603
PMCPMC11223365

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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.