Evidence map›Paper›PMID 39991480›Full record

ArticleInnovation (Cambridge (Mass.))2025

The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals.

Lei-Yun Wang, Bing Yu, Ying Peng, Kai Mou, Yan Zhan, Yi-Min Wang, Wei Ji, Chun Xu, Le-Dong Xiao, Yan Chen and 35 more

Abstract read
In one paragraph

Article in Innovation (Cambridge (Mass.)), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Preventing adverse drug reactions and more: current clinical use of pharmacogenetic testing.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2025
    Article
  7. 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

45 authors.

Lei-Yun WangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Bing YuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Ying PengNational Health Commission Key Laboratory of Birth Defects Research, Prevention and Treatment, Hunan Provincial Maternal and Child Health Care Hospital, Changsha 410000, China.
Kai MouDepartment of Genetic Laboratory, Zibo Maternal and Child Health Hospital, Zibo 255000, China.
Yan ZhanDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Yi-Min WangSalus Med Co. Ltd., Shenzhen 518107, China.
Wei JiFujian Agene Biotechnology Co. Ltd., Fuzhou 350100, China.
Chun XuGenetalks Co. Ltd., Changsha 410008, China.
Le-Dong XiaoXiangya Medical Laboratory, Central South University, Changsha 410078, China.
Yan ChenXiangya Medical Laboratory, Central South University, Changsha 410078, China.
Hua WangThe Hunan Children's Hospital, Changsha 410000, China.
Zhi-Hua SheDepartment of Pharmacy, Hunan Provincial Maternal and Child Health Care Hospital, Changsha 410008, China.
Peng DaiThe Genetics and Prenatal Diagnosis Center, The Department of Obstetrics and Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Gan-Ye ZhaoThe Genetics and Prenatal Diagnosis Center, The Department of Obstetrics and Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Yang WangDepartment of Pharmacy, Xiangya Hospital, Central South University, Changsha 410078, China.
Lu-Lu YuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Miao YuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Ke LiuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Jia-Jia CuiDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Rong LiuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Xi LiDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Yuan-Fei HuangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Zhao-Qian LiuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Dong-Sheng OuyangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Wei ZhangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Qing LiDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Xing-Liang XiongDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Cheng-Xian GuoCenter of Clinical Pharmacology, The Third Xiangya Hospital, Central South University, Changsha 410013, China.
Jin-Gao LiDepartment of Radiation Oncology, Jiangxi Cancer Hospital, Nanchang 330029, China.
Qiao-Li LvDepartment of Radiation Oncology, Jiangxi Cancer Hospital, Nanchang 330029, China.
Qing-He XingChildren's Hospital and Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China.
Hai-Jian WangState Key Laboratory of Genetic Engineering and Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai 200438, China.
Zhi-Ling LiDepartment of Pharmacy, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai 200120, China.
Ji-Chu WuThe Affiliated Shaoyang Hospital, Department of Geriatrics, Hengyang Medical School, University of South China, Shaoyang 422000, China.
Long-Jian HuangYoujiang Medical University for Nationalities, Baise 533000, China.
Jian HeState Key Laboratory of Targeting Oncology, National Center for International Research of Bio-targeting Theranostics, Guangxi Key Laboratory of Bio-targeting Theranostics, Collaborative Innovation Center for Targeting Tumor Diagnosis and Therapy, Guangxi Medical University, Nanning 530021, China.
Li-Ming TanClinical Pharmacy Center, The Second People's Hospital of Huaihua, Huaihua 418000, China.
Wen-Xu HongShenzhen Institute of Dermatology, Shenzhen Center for Chronic Disease Control, Shenzhen 518020, China.
Xue-Chang WangDepartment of Pharmacy, Anning First People's Hospital Affiliated to Kunming University of Science and Technology, Anning 650302, China.
Chao-Peng LiThe First Affiliated Hospital of Shihezi University, Shihezi 832000, China.
Qin LuGeneMind Biosciences Co. Ltd., No. 116, Shenzhen 518000, China.
Long ZhangHunan Jiarun Medical Laboratory Co. Ltd., No. 319, Linyu Road, Yuelu District, Changsha 410000, China.
Xiang-Dong KongThe Genetics and Prenatal Diagnosis Center, The Department of Obstetrics and Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Hong-Hao ZhouDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.
Ji-Ye YinDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pharmacogenomic landscapes and related databases are important for identifying the biomarkers of drug response and toxicity. However, these data are still lacking for the Chinese population. In this study, we constructed a pharmacogenomic landscape and an associated database using whole-genome sequencing data generated by non-invasive prenatal testing in 206,640 Chinese individuals. In total, 1,577,513 variants (including 331,610 novel variants) were identified among 3,538 pharmacogenes related to 2,086 drugs. We found that the variant spectrum in the Chinese population differed among the seven major regions. Regional differences also exist among provinces in China. The average numbers of drug enzyme, transporter, and receptor variants were 258, 557, and 632, respectively. Subsequent correlation analysis indicated that the pharmacogenes affecting multiple drugs had fewer variants. Among the 16 categories of drugs, we found that nervous system, cardiovascular system, and genitourinary system/sex hormone drugs were more likely to be affected by variants of pharmacogenes. Characteristics of the variants in the enzyme, transporter, and receptor subfamilies showed specificity. To explore the clinical utility of these data, a genetic association study was conducted on 1,019 lung cancer patients. Two novel variants,

Indexed as

Chinesedatabasenext-generation sequencepharmacogenespharmacogenomicsvariants

Identifiers

PMID39991480
PMCPMC11846038

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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.