Evidence map›Paper›PMID 29748863›Full record

ArticleEuropean journal of clinical pharmacology2018

Repaglinide-irbesartan drug interaction: effects of SLCO1B1 polymorphism on repaglinide pharmacokinetics and pharmacodynamics in Chinese population.

Qi Pei, Jun-Yan Liu, Ji-Ye Yin, Guo-Ping Yang, Shi-Kun Liu, Yi Zheng, Pan Xie, Cheng-Xian Guo, Mi Luo, Hong-Hao Zhou and 2 more

Abstract read
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In one paragraph

Article in European journal of clinical pharmacology, 2018. 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
0.5field-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

7 citing papers in PubMed, 16 citations in OpenAlex.

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  6. Pharmacogenomic Studies of Current Antidiabetic Agents and Potential New Drug Targets for Precision Medicine of Diabetes.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2020
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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 4 institutions in 1 country.

Qi PeiDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Jun-Yan LiuXiangya School of Medicine, Central South University, Changsha, 410078, Hunan, People's Republic of China.
Ji-Ye YinDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Guo-Ping YangDepartment of Pharmacy, The Third Xiangya Hospital, Central South University, Changsha, 410013, Hunan, People's Republic of China.
Shi-Kun LiuDepartment of Pharmacy, The Third Xiangya Hospital, Central South University, Changsha, 410013, Hunan, People's Republic of China.
Yi ZhengDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Pan XieDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Cheng-Xian GuoDepartment of Pharmacy, The Third Xiangya Hospital, Central South University, Changsha, 410013, Hunan, People's Republic of China.
Mi LuoDepartment of Pharmacy, The Third Xiangya Hospital, Central South University, Changsha, 410013, Hunan, People's Republic of China.
Hong-Hao ZhouDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Xi LiDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China. lixi6931430@126.com.
Zhao-Qian LiuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China. liuzhaoqian63@126.com.
Central South University · CNPharmacoGenetics (China) · CNThird Xiangya Hospital · CNXiangya Hospital Central South University · CN

Funding

National Natural Science Foundation of China 81373490, 81573463, 81573508the National Key Research and Development Programs 2016YFC1306900, 2016YFC0905002, 2016YFC1201805The Strategy-Oriented Special Project of Central South University in China ZLXD2017003
6 · The paper itself

Abstract

purposeOn account of the potential inhibition of OATP1B1 (organic anion transporting polypeptide) by angiotensin II receptor blockers (ARBs) and the effects of SLCO1B1 (solute carrier organic anion transporter family member) polymorphism, the aim of current study is to assess the impact of ARBs on the pharmacokinetics (PK) and pharmacodynamics (PD) of repaglinide in Chinese healthy volunteers with different SLCO1B1 genotypes.

methodsThe in vitro study was conducted on irbesartan, valsartan, olmesartan, and losartan by using HEK293 cells transfected with OATP1B1. Data on drug interactions between repaglinide and irbesartan from 21 healthy Chinese-Han male volunteers were collected and analyzed.

resultsIC

conclusionSLCO1B1 c.521 T>C polymorphism affects the PK of repaglinide in Chinese population. Irbesartan increased repaglinide exposure in subjects with SLCO1B1 c.521 TT genotype, but not SLCO1B1 c.521 TC genotype.

Indexed as

AdultAsian PeopleBiphenyl CompoundsBlood GlucoseCarbamatesCells, CulturedChinaDose-Response Relationship, DrugDrug InteractionsGenotypeHealthy VolunteersHumansImidazolesIrbesartanLiver-Specific Organic Anion Transporter 1LosartanBiphenyl CompoundsBlood GlucoseCarbamatesImidazolesIrbesartanLiver-Specific Organic Anion Transporter 1LosartanolmesartanPiperidinesrepaglinideSLCO1B1 protein, humanTetrazolesValsartanDrug interactionsIrbesartanPharmacodynamicsPharmacokineticsPolymorphismRepaglinideSLCO1B1

Identifiers

PMID29748863
OpenAlexW2799748210

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.