Previous Page  14 / 14
Information
Show Menu
Previous Page 14 / 14
Page Background

Page 32

Notes:

allied

academies

Curr Trend Cardiol. 2017 | Volume 1 Issue 3

September 18-19, 2017 | Toronto, Canada

Annual Conference on

HEART DISEASES

Backgrounds and aims

: Cholesterol 7α hydroxylase encoding

by gene CYP7A1 is the initial and rate-limiting step in the

classical bile acid synthesis pathway. Atorvastatin can markedly

upregulate the mRNAs of bile acids synthetic enzymes

CYP7A1 in the liver to increase fecal bile acid excretion. We

tempt to investigate the association between a novel CYP7A1

polymorphism rs8192875 and reduction of lipid levels response

to atorvastatin in Chinese patients with coronary artery disease.

Methods

: Of 169 patients with coronary artery disease

were treated with atorvastatin for one month. Lipid profiles,

including triglycerides(TGs), total cholesterol(TC), low-

density lipoprotein cholesterol(LDL-C), and high-density

lipoprotein cholesterol(HDL-C) were determined before and

after treatment. Rs8192875 genotypes were assayed with

the iPLEX assay in conjunction with the MassARRAY platform.

We performed independent sample t test or Kruskal-Wallis

test to evaluate the effects of SNP.

Results

: After one month of atorvastatin therapy, the lipid

levels decreased significantly. Compared with AG genotype,

the GG genotype of rs8192875 achieved a greater reduction

of LDL-C level (0.694±0.701 vs. 0.136±0.401 mmol/l,

p=0.0056; 24.090±23.104% vs. 2.182±20.809%, p=0.0031);

and a similar pattern of efficacy appears to TC (0.808±0.791

vs. 0.302±0.381 mmol/l, p=0.0208; 16.410±15.370% vs.

6.936±9.711%, p=0.0341).The genotypes had no significant

difference on TGs or HDL cholesterol-lowering response to

atorvastatin.

Conclusions

: A novel CYP7A1 exon variant rs8192875 is

significantly associated with reducing LDL-C and TC level

response to atorvastatin.

Speaker Biography

Jing Chen completed her Master’s degree in Epidemiology and Hygenic statistics

from School of Public Health, Peking University Health Science Center in 2016. She

participated in a research study at Shi Mao Group Charity Hospital Research as an

investigator. Her other research experiences include- National Free Preconception

Health Examinaton Project (NFPHEP) during, The Family Based Cohort Study on

The Common Non-communicable Chronic Diseases of the Population in The Rural

Community of Northern China during and WHO project on “To promote the quality of

Chinese maternal and child health annual report research”.

e:

807706116@qq.com

A novel CYP7A1 polymorphism is associated with the low-density lipoprotein cholesterol response to

atorvastatin

Jing Chen

1

, Zhi-Ke Liu,

2

Da-Fang Chen,

2

1

Peking University Six Hospital, China

2

Peking University Health Science Center, China