- Home
- Featured Publications
- Center Publications
- Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific manner.
Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific manner.
Citation | “Statin-Induced Expression Change Of Insig1 In Lymphoblastoid Cell Lines Correlates With Plasma Triglyceride Statin Response In A Sex-Specific Manner.”. The Pharmacogenomics Journal, pp. 222-229. . |
Center | UCSD-UCLA |
Author | E Theusch, K Kim, K Stevens, J D Smith, Y-D I Chen, J I Rotter, D A Nickerson, M W Medina |
Abstract |
Statins are widely prescribed to lower plasma low-density lipoprotein (LDL) cholesterol levels. They also modestly reduce plasma triglyceride (TG), an independent cardiovascular disease risk factor, in most people. The mechanism and inter-individual variability of TG statin response is poorly understood. We measured statin-induced gene expression changes in lymphoblastoid cell lines derived from 150 participants of a simvastatin clinical trial and identified 23 genes (false discovery rate, FDR=15%) with expression changes correlated with plasma TG response. The correlation of insulin-induced gene 1 (INSIG1) expression changes with TG response (rho=0.32, q=0.11) was driven by men (interaction P=0.0055). rs73161338 was associated with INSIG1 expression changes (P=5.4 × 10) and TG response in two statin clinical trials (P=0.0048), predominantly in men. A combined model including INSIG1 expression level and splicing changes accounted for 29.5% of plasma TG statin response variance in men (P=5.6 × 10). Our results suggest that INSIG1 variation may contribute to statin-induced changes in plasma TG in a sex-specific manner. |
Year of Publication |
2017
|
Journal |
The pharmacogenomics journal
|
Volume |
17
|
Issue |
3
|
Number of Pages |
222-229
|
Date Published |
12/2017
|
ISSN Number |
1473-1150
|
DOI |
10.1038/tpj.2016.12
|
Alternate Journal |
Pharmacogenomics J.
|
PMID |
26927283
|
PMCID |
PMC5008997
|
Download citation |