Evidence map›Paper›PMID 30283089›Full record

ArticleJournal of human hypertension2018

A gender-specific association of the polymorphism Ile197Met in the kininogen 1 gene with plasma irbesartan concentrations in Chinese patients with essential hypertension.

Shengnan Hu, Jun Cheng, Justin Weinstock, Xiu Fan, Scott A Venners, Yi-Hsiang Hsu, Suwen Wu, Faming Pan, Xiangdong Zha, Jinlu Sun and 2 more

Abstract read
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In one paragraph

Article in Journal of human hypertension, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 85% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

12 authors at 7 institutions in 3 countries.

Shengnan HuSchool of Life Sciences, Anhui University, Hefei, China.
Jun ChengSchool of Life Sciences, Anhui University, Hefei, China.
Justin WeinstockDepartment of Statistics, University of Virginia, Charlottesville, VA, USA.
Xiu FanSchool of Life Sciences, Anhui University, Hefei, China.
Scott A VennersFaculty of Health Sciences, Simon Fraser University, Burnaby, BC, Canada.
Yi-Hsiang HsuInstitute for Aging Research and Harvard Medical School, Boston, MA, USA.
Suwen WuSchool of Life Sciences, Anhui University, Hefei, China.
Faming PanDepartment of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, China.
Xiangdong ZhaSchool of Life Sciences, Anhui University, Hefei, China.
Jinlu SunDepartment of Allergy, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China. sunjl5@yahoo.com.
Shanqun JiangSchool of Life Sciences, Anhui University, Hefei, China. shanqunjiang2014@163.com.ORCID http://orcid.org/0000-0003-2602-3449
Xiping XuInstitute of Biomedicine, Anhui Medical University, Hefei, China.
Anhui University · CNAnhui Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNHarvard University · USSimon Fraser University · CAUniversity of Science and Technology of China · CNUniversity of Virginia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study was conducted to explore interactions in the association of the kininogen (KNG1) Ile197Met polymorphism and gender with plasma concentrations of irbesartan in Chinese patients with essential hypertension. A total of 1100 subjects with essential hypertension received a daily oral dose of 150 mg irbesartan for twenty-eight consecutive days. High-performance liquid chromatography-fluorescence (HPLC) was used to detect plasma irbesartan concentrations on day 28. The KNG1 Ile197Met gene polymorphism was determined using high-throughput TaqMan technology. The frequency distribution of KNG1 Ile197Met genotype conformed to the Hardy-Weinberg equilibrium. After 28 days of treatment, patients with the GG genotype had significantly lower irbesartan concentrations (P = 0.033) compared to homozygous TT genotype carriers. After stratifying by gender, male G allele carriers had significantly lower irbesartan concentrations (GG, P = 0.015; TG, P = 0.015, respectively) relative to TT genotype after adjusting for age, region, body mass index (BMI), smoking, and alcohol consumption. However, there was no significant difference in female subjects. A further test for a multiplicative interaction between the KNG1 Ile197Met polymorphism and gender in association with ln-plasma irbesartan concentrations in a multiple linear regression model was also significant (P for interaction = 0.033). This is the first study to suggest that gender may influence the association of the Ile197Met variant of KNG1 with ln-plasma irbesartan concentration. This finding may indicate that the interaction of gender and the KNG1 Ile197Met gene polymorphism can influence plasma trough irbesartan concentrations, which may contribute to a better development of personalized hypertensive treatment in Chinese patients.

Indexed as

Asian PeopleEssential HypertensionFemaleHumansIrbesartanKininogensMaleMiddle AgedPharmacogenomic TestingPolymorphism, Single NucleotideProspective StudiesSex FactorsIrbesartanKininogensKNG1 protein, human

Identifiers

PMID30283089
OpenAlexW2895756572

What OpenQuestion holds

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Registered trials

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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.