Literature DB >> 18845302

LDL-cholesterol lowering increases plasma apelin in isolated hypercholesterolemia.

Ilker Tasci1, Gokhan Erdem, Gokhan Ozgur, Serkan Tapan, Teoman Dogru, Halil Genc, Cengizhan Acikel, Taner Ozgurtas, Alper Sonmez.   

Abstract

Apelin, a relatively newer adipokine with various actions in cardiovascular system, was recently reported to decrease in dyslipidemia. The present study addresses whether plasma apelin increases after hypolipidemic intervention either through therapeutic life style change (TLC) or statin treatment. A total of 134 patients were subjected to treatment with a TLC intervention for 12 weeks. Of these, 116 successfully completed the period, and LDL-cholesterol level decreased to target level (<160 mg/dL) in 54 (46.5%) individuals. The remaining 62 patients were treated with rosuvastatin for 12 weeks, and 56 of them finished the study. Circulating apelin, adiponectin, leptin, TNF-alpha, hsCRP and insulin levels were determined both at baseline and after TLC intervention and statin treatment. There was no significant change in plasma apelin concentration in patients unresponsive to TLC (p=0.110). LDL-cholesterol lowering either through TLC or statin treatment was accompanied by an increase in plasma apelin (p=0.000, p=0.020) and adiponectin (p=0.001, p=0.011). Serum leptin decreased after successful TLC (p=0.042/male, p=0.023/female) but not after statin treatment (p=0.959/male, p=0.134/female). Serum TNF-alpha (p=0.902) and plasma hsCRP (p=0.135) levels remained unchanged after TLC intervention but decreased after statin treatment (p=0.000, p=0.023, respectively). Plasma insulin and homeostasis model assessment scores decreased after TLC (p=0.000 for both) but not rosuvastatin treatment (p=0.865, p=0.722, respectively). In conclusion, independent of the type of treatment, reduction in LDL-cholesterol levels in otherwise healthy people with isolated dyslipidemia results in an increase in plasma apelin concentration. More experiments may show a substantial role for this peptide in the mechanism of atherosclerosis.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18845302     DOI: 10.1016/j.atherosclerosis.2008.08.030

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  6 in total

1.  Apelin/APJ signaling is a critical regulator of statin effects in vascular endothelial cells--brief report.

Authors:  Danielle L McLean; Jongmin Kim; Yujung Kang; Hong Shi; G Brandon Atkins; Mukesh K Jain; Hyung J Chun
Journal:  Arterioscler Thromb Vasc Biol       Date:  2012-09-20       Impact factor: 8.311

2.  Apelin levels are increased in morbidly obese subjects with type 2 diabetes mellitus.

Authors:  Federico Soriguer; Lourdes Garrido-Sanchez; Sara Garcia-Serrano; Jose M Garcia-Almeida; Juan Garcia-Arnes; Francisco J Tinahones; Eduardo Garcia-Fuentes
Journal:  Obes Surg       Date:  2009-09-15       Impact factor: 4.129

3.  The impact of aerobic exercise training on novel adipokines, apelin and ghrelin, in patients with type 2 diabetes.

Authors:  Nikolaos P E Kadoglou; Ioannis S Vrabas; Alkistis Kapelouzou; Stilianos Lampropoulos; Nikolaos Sailer; Alkiviadis Kostakis; Christos D Liapis; Nikoletta Angelopoulou
Journal:  Med Sci Monit       Date:  2012-05

4.  Apelin, Nitric Oxide and Vascular Affection in Adolescent Type 1 Diabetic Patients.

Authors:  Soha M Abd El Dayem; Ahmed A Battah; Abo El Maged El Bohy; Rash Nazih Yousef; Azza M Ahmed; Ahmed A Talaat
Journal:  Open Access Maced J Med Sci       Date:  2017-12-04

Review 5.  The Role of Apelin-APJ System in Diabetes and Obesity.

Authors:  Cheng Li; Hongna Cheng; Binay Kumar Adhikari; Shudong Wang; Na Yang; Wenyun Liu; Jian Sun; Yonggang Wang
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-09       Impact factor: 5.555

6.  Serum adipokine levels in the obese people.

Authors:  Ilker Tasci; Teoman Dogru; Gokhan Erdem; Serkan Tapan; Cemal Nuri Ercin; Alper Sonmez
Journal:  Int J Biol Sci       Date:  2009-04-03       Impact factor: 6.580

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.