Evidence map›Paper›PMID 29556032›Full record

ArticleJournal of human genetics2018

Common variant rs11191548 near the CYP17A1 gene is associated with hypertension and the serum 25(OH) D levels in Han Chinese.

Ning Zhang, Jian Jia, Qiuju Ding, Huimei Chen, Xiaoman Ye, Haixia Ding, Yiyang Zhan

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of human genetics, 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
0.3field-weighted citation impact, top 38% 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, 7 citations in OpenAlex.

  1. Associations Between Cytochrome P450 (CYP) Gene Single-Nucleotide Polymorphisms and Second-to-Fourth Digit Ratio in Chinese University Students.Medical science monitor : international medical journal of experimental and clinical research · 2021
    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

7 authors at 3 institutions in 1 country.

Ning ZhangGeriatric Medicine Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Jian JiaGeneral Medicine Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Qiuju DingJiangsu Key Laboratory of Molecular Medicine, Department of Medical Genetics, Nanjing University, Nanjing, Jiangsu, China.
Huimei ChenJiangsu Key Laboratory of Molecular Medicine, Department of Medical Genetics, Nanjing University, Nanjing, Jiangsu, China.
Xiaoman YeGeriatric Medicine Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Haixia DingGeriatric Medicine Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China. dhxnjmu@126.com.
Yiyang ZhanGeriatric Medicine Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China. yiyangzhan@sina.com.
Jiangsu Province Hospital · CNNanjing Medical University · CNNanjing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CYP17A1 gene, which encodes17α-hydroxylase and 17,20-lyase, has been identified as a common hypertension susceptibility locus in a European population. However, the association between CYP17A1 polymorphisms and hypertension is unclear in the Chinese population as well as in the role of serum 25(OH) D levels. Six single nucleotide polymorphisms (SNPs) in CYP17A1 were genotyped in two stages in a Han Chinese population, and the serum 25(OH) D levels were measured. Analysis in stage 1 showed that the rs1004467 minor G-allele and rs11191548 minor C-allele in CYP17A1 were significantly associated with a decreased risk of hypertension and higher serum 25(OH) D levels (all P < 0.05). The larger sample in stage 2 also showed that a mutation in rs11191548 was significantly associated with a decreased risk of hypertension (adjusted OR = 0.707, 95% CI: 0.553-0.904, P = 0.006). The rs11191548 minor C-allele was associated with higher serum 25(OH) D levels in hypertensive subjects (βadj ± SEM = 0.094 ± 0.949, P = 0.003) and controls (βadj ± SEM = 0.128 ± 1.025, P < 0.001). In conclusion, the rs11191548 CYP17A1 gene mutation was associated with hypertension and the serum 25(OH) D levels in Han Chinese.

Indexed as

Polymorphism, Single NucleotideAllelesAsian PeopleChinaEssential HypertensionEthnicityFemaleGenes, DominantGenes, RecessiveGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedMutationQuantitative Trait Loci25-hydroxyvitamin DCYP17A1 protein, humanSteroid 17-alpha-HydroxylaseVitamin D

Identifiers

PMID29556032
OpenAlexW2796123900

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.