Evidence map›Paper›PMID 15148588›Full record

ArticleJournal of human genetics2004

D919G polymorphism of methionine synthase gene is associated with blood pressure response to benazepril in Chinese hypertensive patients.

Yan Zhang, Minmin Zhang, Tianhua Niu, Xin Xu, Guoying Zhu, Yong Huo, Changzhong Chen, Xiaobin Wang, Houxun Xing, Shaojie Peng and 3 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Journal of human genetics, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 32% of its field
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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  3. Review
  4. 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

13 authors at 5 institutions in 2 countries.

Yan ZhangDepartment of Cardiology, Peking University First Hospital, Beijing, 100034, China.
Minmin ZhangSchool of Life Science, University of Science and Technology in China, Hefei, China.
Tianhua NiuProgram for Population Genetics, Harvard School of Public Health, 665 Huntington Ave., FXB-101, Boston, MA, 02115, USA.
Xin XuProgram for Population Genetics, Harvard School of Public Health, 665 Huntington Ave., FXB-101, Boston, MA, 02115, USA.
Guoying ZhuDepartment of Cardiology, Peking University First Hospital, Beijing, 100034, China.
Yong HuoDepartment of Cardiology, Peking University First Hospital, Beijing, 100034, China.
Changzhong ChenProgram for Population Genetics, Harvard School of Public Health, 665 Huntington Ave., FXB-101, Boston, MA, 02115, USA.
Xiaobin WangThe Mary Ann and J. Milburn Smith Child Health Program, Children's Memorial Hospital and Children's Memorial Institute for Education and Research (CMIER), Chicago, IL, 60614, USA.
Houxun XingInstitute of Biomedicine, Anhui Medical University, Hefei, China.
Shaojie PengInstitute of Biomedicine, Anhui Medical University, Hefei, China.
Aiqun HuangSchool of Life Science, University of Science and Technology in China, Hefei, China.
Xiumei HongSchool of Life Science, University of Science and Technology in China, Hefei, China.
Xiping XuProgram for Population Genetics, Harvard School of Public Health, 665 Huntington Ave., FXB-101, Boston, MA, 02115, USA. xu@hsph.harvard.edu.
Harvard University · USPeking University · CNUniversity of Science and Technology of China · CNAnhui Medical University · CNLurie Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Individual variation in drug response is considered to have multiple origins arising from interactions among susceptible genes and environmental factors. A total of 726 hypertensive patients who took benazepril 10 mg once a day for 15 days and their families from Huoqiu county of Anhui Province, China, were used to study the association between D919G polymorphism of methionine synthase (MTR) gene and the antihypertensive effect of this angiotensin-converting enzyme inhibitor. Compared to the 919D allele, both population-based ( P=0.010) and family-based association tests (additive model P=0.018, dominant model P=0.025) demonstrated that the 919G allele was associated with a significantly less diastolic blood pressure reduction. No significant association was found between the extent of systolic blood pressure reduction and benazepril therapy. Our finding suggests that the D919G polymorphism of the MTR gene may be a useful genetic marker to predict the antihypertensive effect of short-term benazepril therapy in hypertensive patients of Anhui Province, China.

Indexed as

Polymorphism, Genetic5-Methyltetrahydrofolate-Homocysteine S-MethyltransferaseAdultAgedAllelesAntihypertensive AgentsBenzazepinesBlood PressureChinaEnvironmentFemaleGenotypeHumansMaleMiddle AgedPhenotype5-Methyltetrahydrofolate-Homocysteine S-MethyltransferaseAntihypertensive AgentsbenazeprilBenzazepines

Identifiers

PMID15148588
OpenAlexW1995908738

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.