Ontology type: schema:ScholarlyArticle Open Access: True
2014-04-01
AUTHORSTsuyoshi Nozue, Shingo Yamamoto, Shinichi Tohyama, Kazuki Fukui, Shigeo Umezawa, Yuko Onishi, Tomoyuki Kunishima, Akira Sato, Toshihiro Nozato, Shogo Miyake, Youichi Takeyama, Yoshihiro Morino, Takao Yamauchi, Toshiya Muramatsu, Kiyoshi Hibi, Mitsuyasu Terashima, Ichiro Michishita
ABSTRACTBackgroundStatin therapy results in regression and stabilization of coronary artery plaques, and reduces the incidence of coronary artery disease. However, statin therapy does not effectively halt the accumulation of necrotic core in all patients. The purpose of the present study was to identify the predictors associated with necrotic core progression during statin therapy.MethodsCoronary atherosclerosis in non-culprit lesions was evaluated using virtual histology intravascular ultrasound at baseline and 8 months after statin therapy. One hundred nineteen patients were divided into 2 groups based on necrotic core progression or regression during an 8-month follow-up period.ResultsPatients with necrotic core progression had higher serum lipoprotein(a) [Lp(a)] levels than patients with regression at baseline (16 mg/dL vs. 12 mg/dL, p = 0.02) and at the 8-month follow-up (17 mg/dL vs. 10 mg/dL, p = 0.006). Patients with necrotic core progression had a higher fibro-fatty plaque volume (1.28 mm3/mm vs. 0.73 mm3/mm, p = 0.002), and less necrotic core (0.56 mm3/mm vs. 1.04 mm3/mm, p < 0.0001) and dense calcium (0.35 mm3/mm vs. 0.56 mm3/mm, p = 0.006) plaque volumes at baseline than patients with regression. Multivariate logistic regression analysis showed that Lp(a) was a significant independent predictor associated with necrotic core progression during statin therapy (odds ratio [OR]: 3.514; 95% confidence interval [CI]: 1.338-9.228; p = 0.01).ConclusionsSerum Lp(a) is independently associated with necrotic core progression in statin-treated patients with angina pectoris. More... »
PAGES59
http://scigraph.springernature.com/pub.10.1186/1476-511x-13-59
DOIhttp://dx.doi.org/10.1186/1476-511x-13-59
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PUBMEDhttps://www.ncbi.nlm.nih.gov/pubmed/24684829
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"description": "BackgroundStatin therapy results in regression and stabilization of coronary artery plaques, and reduces the incidence of coronary artery disease. However, statin therapy does not effectively halt the accumulation of necrotic core in all patients. The purpose of the present study was to identify the predictors associated with necrotic core progression during statin therapy.MethodsCoronary atherosclerosis in non-culprit lesions was evaluated using virtual histology intravascular ultrasound at baseline and 8\u00a0months after statin therapy. One hundred nineteen patients were divided into 2 groups based on necrotic core progression or regression during an 8-month follow-up period.ResultsPatients with necrotic core progression had higher serum lipoprotein(a) [Lp(a)] levels than patients with regression at baseline (16\u00a0mg/dL vs. 12\u00a0mg/dL, p\u2009=\u20090.02) and at the 8-month follow-up (17\u00a0mg/dL vs. 10\u00a0mg/dL, p\u2009=\u20090.006). Patients with necrotic core progression had a higher fibro-fatty plaque volume (1.28\u00a0mm3/mm vs. 0.73\u00a0mm3/mm, p\u2009=\u20090.002), and less necrotic core (0.56\u00a0mm3/mm vs. 1.04\u00a0mm3/mm, p\u2009<\u20090.0001) and dense calcium (0.35\u00a0mm3/mm vs. 0.56\u00a0mm3/mm, p\u2009=\u20090.006) plaque volumes at baseline than patients with regression. Multivariate logistic regression analysis showed that Lp(a) was a significant independent predictor associated with necrotic core progression during statin therapy (odds ratio [OR]: 3.514; 95% confidence interval [CI]: 1.338-9.228; p\u2009=\u20090.01).ConclusionsSerum Lp(a) is independently associated with necrotic core progression in statin-treated patients with angina pectoris.",
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