Independent Link Between Levels of Proprotein Convertase Subtilisin/Kexin Type 9 and FABP4 in a General Population Without Medication

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• 作者：Masato Furuhashi ; MD ; PhD^a ; ^{furuhasi@sapmed.ac.jp" class="auth_mail" title="E-mail the corresponding author} ; Akina Omori ; PhD^a ; Megumi Matsumoto ; BSc^a ; Yu Kataoka ; MD ; PhD^b ; Marenao Tanaka ; MD ; PhD^a ; Norihito Moniwa ; MD ; PhD^a ; Hirofumi Ohnishi ; MD ; PhD^a ; ^c ; Hideaki Yoshida ; MD ; PhD^a ; Shigeyuki Saitoh ; MD ; PhD^a ; ^d ; Kazuaki Shimamoto ; MD ; PhD^e ; Tetsuji Miura ; MD ; PhD^a
• 刊名：The American Journal of Cardiology
• 出版年：2016
• 出版时间：15 July 2016
• 年：2016
• 卷：118
• 期：2
• 页码：198-203
• 全文大小：455 K

文摘

Proprotein convertase subtilisin/kexin type 9 (PCSK9) binds to and degrades the low-density lipoprotein (LDL) receptor, leading to hypercholesterolemia and cardiovascular risk. Fatty acid binding protein 4 (FABP4/adipocyte FABP/aP2) is secreted from adipocytes in association with lipolysis, and circulating FABP4 has been reported to act as an adipokine for the development of insulin resistance and atherosclerosis. Elevated serum FABP4 level is associated with obesity, insulin resistance, dyslipidemia, and atherosclerosis. In this study, we examined the association between circulating levels of FABP4 and PCSK9 in a general population. A total of 265 subjects (male/female: 98/167) who were not on medication were recruited from subjects of the Tanno-Sobetsu Study, and concentrations of FABP4 and PCSK9 were measured. The level of FABP4, but not that of PCSK9, showed a gender difference, being higher in women than in men. FABP4 level was independently associated with gender, adiposity, renal dysfunction, and levels of cholesterol and PCSK9. There was a significant and gender-different correlation between PCSK9 level and age: negatively in men (r = −0.250, p = 0.013) and positively in women (r = 0.183, p = 0.018). After adjustment of age, gender, and LDL cholesterol level, PCSK9 level was positively and independently correlated with FABP4 concentration. In conclusion, PCSK9 level is differentially regulated by gender during aging. Circulating FABP4 is independently associated with the PCSK9 level, suggesting that elevation of FABP4 level as an adipokine leads to dyslipidemia through increased PCSK9 level and subsequent degradation of the LDL receptor.