Evidence map›Paper›PMID 30215102›Full record

ArticleEuropean journal of clinical pharmacology2019

FKBP1A rs6041749 polymorphism is associated with allograft function in renal transplant patients.

Zhuo Wu, Qinxia Xu, Xiaoyan Qiu, Luyang Xu, Zheng Jiao, Ming Zhang, Mingkang Zhong

Abstract read
PubMed Publisher
In one paragraph

Article in European journal of clinical pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Biomedicines · 2024
    Article
  4. Article
  5. Recent Advances on Biomarkers of Early and Late Kidney Graft Dysfunction.International journal of molecular sciences · 2020
    Review
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

7 authors at 2 institutions in 1 country.

Zhuo WuDepartment of Pharmacy, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, China.
Qinxia XuDepartment of Pharmacy, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, China.
Xiaoyan QiuDepartment of Pharmacy, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, China. xyqiu@163.com.
Luyang XuDepartment of Pharmacy, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, China.
Zheng JiaoDepartment of Pharmacy, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, China.
Ming ZhangDepartment of Nephrology, Huashan Hospital, Fudan University, Shanghai, China.
Mingkang ZhongDepartment of Pharmacy, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, China.
Huashan Hospital · CNFudan University · CN

Funding

National Natural Science Foundation of China No. 81302854National Natural Science Foundation of China No. 81573505Natural Science Foundation of Shanghai No. 13ZR1405200the Guidance Project of Shanghai Municipal Science and Technology Commission 15411968000"Weak Discipline Construction Project" of Shanghai Municipal Commission of Health and Family Planning No.2016ZB0301-01
6 · The paper itself

Abstract

aimTo investigate the potential impact of single-nucleotide polymorphisms (SNPs) in the FK506-binding protein (FKBP)-calcineurin (CaN)-nuclear factor of activated T cells (NFAT) signaling pathway on the efficacy and safety of tacrolimus (TAC) in Chinese renal transplant patients.

methodsSeventy-seven tag SNPs were detected in 146 patients who were on TAC-based maintenance immunosuppression and who followed up for at least 2 years. The relationships of these polymorphisms with clinical outcomes such as acute rejection, acute nephrotoxicity, pneumonia, and estimated glomerular filtration rate (eGFR) were explored. For the FKBP1A rs6041749 polymorphism, which has a significant association with renal function over time, a preliminary functional analysis was performed using a dual-luciferase reporter gene system.

resultsThe patients with FKBP1A rs6041749 TT genotype had a more stable eGFR level than CC and CT carriers (P = 2.08 × 10

conclusionsFKBP1A rs6041749 C allele carriers are at higher risk for eGFR deterioration. The variant might serve as a biomarker to predict allograft function in renal transplant patients.

Indexed as

AdultAsian PeopleBiomarkersFemaleFollow-Up StudiesGlomerular Filtration RateGraft RejectionHumansImmunosuppressive AgentsKidney TransplantationMaleMiddle AgedPolymorphism, Single NucleotideTacrolimusTacrolimus Binding ProteinsBiomarkersFKBP1A protein, humanImmunosuppressive AgentsTacrolimusTacrolimus Binding ProteinseGFRFKBPPolymorphismsRenal transplantationTacrolimus

Identifiers

PMID30215102
OpenAlexW2890598694

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.