Evidence map›Paper›PMID 24413999›Full record

ArticleMolecular biology reports2014

Association study of common variations of FBN1 gene and essential hypertension in Han Chinese population.

Jinfeng Chen, Song Yang, Xianghai Zhao, Jiahui Shen, Hairu Wang, Yanchun Chen, Yanni Ji, Wen Wang, Wei Zhou, Xuecai Wang and 7 more

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Article in Molecular biology reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.9field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

17 authors at 6 institutions in 1 country.

Jinfeng ChenDepartment of Epidemiology and Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, 210029, China.
Song Yang
Xianghai Zhao
Jiahui Shen
Hairu Wang
Yanchun Chen
Yanni Ji
Wen Wang
Wei Zhou
Xuecai Wang
Junming Tang
Xiangfeng Lu
Shufeng Chen
Laiyuan Wang
Hongfan Li
Chong Shen
Yanping Zhao
Jiangsu University · CNNanjing Medical University · CNYixing People's Hospital · CNChinese National Human Genome Center · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNPeking Union Medical College Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibrillin-1 (FBN1) was reported to have impact on the physiological arterial stiffness and vascular remodeling with hypertension of recent years. In the previous study we reported the association of four functional single nucleotide polymorphisms (SNPs) of FBN1 gene and hypertension. Here, we further investigate the association of four tagging SNPs (tagSNPs) which covered remain genetic variation blocks of FBN1 gene with hypertension, blood pressure and efficacy of antihypertensive in a South Han Chinese population. A case-control study including 2,012 hypertension cases and 2,116 controls age- and sex-matched controls was conducted from a community-based population and four candidate tagSNPs of the FBN1 gene were genotyped. Association analysis by multiple logistic regression was conducted for allele, genotype and haplotype and hypertension, blood pressure trait and control status with antihypertensive. General linear model was applied to compare blood pressure levels between genotypes. The association of rs17361868 and hypertension was statistically significant and that was further observed in female, ≥55 years, non-smoking and non-drinking populations (P < 0.05). Significant association of rs668842, rs11635140 and hypertension were observed in <55 years population as well as the later in female and non-smoking populations respectively. Haplotype G-T constructed of rs668842 and rs11635140 was significantly associated with hypertension comparing to reference haplotype A-C (P = 0.022). Normally distributed square root of TGF-β1 (pg/ml) of hypertension cases (148.56 ± 66.46) was significantly higher than that of control (128.52 ± 65.11), P = 0.008. Furthermore, TGF-β1 was significantly correlated with SBP (r = 0.135, P = 0.018) and DBP (r = 0.154, P = 0.007) respectively whereas no statistical difference of blood pressure or TGF-β1 was observed between genotypes. Remarkably, rs17361868 were significantly associated with the status of blood pressure in the patients taking three of the antihypertensive drugs, Zhen Ju Jiang Ya tablets, Jiang Ya tablet and compound reserpine (P < 0.05). The present study provides further association evidence of FBN1 gene polymorphisms and hypertension, antihypertensive efficacy. Further replication of these results via association or prospective studies conducted in other populations is warranted.

Indexed as

Genetic VariationAdipokinesAgedAllelesAsian PeopleBlood PressureCase-Control StudiesChinaEssential HypertensionFemaleFibrillin-1FibrillinsGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeAdipokinesFBN1 protein, humanFibrillin-1FibrillinsMicrofilament ProteinsTransforming Growth Factor beta1

Identifiers

PMID24413999
OpenAlexW1988682083

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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.