TY - JOUR
T1 - PCSK9 and diabetes
T2 - Is there a link?
AU - Momtazi, Amir Abbas
AU - Banach, Maciej
AU - Pirro, Matteo
AU - Stein, Evan A.
AU - Sahebkar, Amirhossein
PY - 2017/6
Y1 - 2017/6
N2 - Diabetes mellitus (DM) is associated with an increased risk of cardiovascular disease (CVD). Inhibitors of proprotein convertase subtilisin/kexin type 9 (PCSK9) have emerged as effective low-density lipoprotein cholesterol-lowering compounds. Although the results of available epidemiological, preclinical, and clinical studies suggest a positive association of plasma PCSK9 levels with glycemic parameters and risk of type 2 DM (T2DM), genetic findings have shown contradictory results. Overall, the impact of PCSK9 inhibitors on glycemic control parameters in patients with DM remains unclear. Here, we assess the available evidence for the association of PCSK9 status with the incidence and control of DM in preclinical and clinical studies, and identify molecular mechanisms regulating PCSK9 expression in the diabetic state. Here, we provide a comprehensive overview of preclinical and clinical studies on the role of PCSK9 and PCSK9 inhibition in diabetes.
AB - Diabetes mellitus (DM) is associated with an increased risk of cardiovascular disease (CVD). Inhibitors of proprotein convertase subtilisin/kexin type 9 (PCSK9) have emerged as effective low-density lipoprotein cholesterol-lowering compounds. Although the results of available epidemiological, preclinical, and clinical studies suggest a positive association of plasma PCSK9 levels with glycemic parameters and risk of type 2 DM (T2DM), genetic findings have shown contradictory results. Overall, the impact of PCSK9 inhibitors on glycemic control parameters in patients with DM remains unclear. Here, we assess the available evidence for the association of PCSK9 status with the incidence and control of DM in preclinical and clinical studies, and identify molecular mechanisms regulating PCSK9 expression in the diabetic state. Here, we provide a comprehensive overview of preclinical and clinical studies on the role of PCSK9 and PCSK9 inhibition in diabetes.
UR - http://www.scopus.com/inward/record.url?scp=85011301421&partnerID=8YFLogxK
U2 - 10.1016/j.drudis.2017.01.006
DO - 10.1016/j.drudis.2017.01.006
M3 - Review article
C2 - 28111330
AN - SCOPUS:85011301421
SN - 1359-6446
VL - 22
SP - 883
EP - 895
JO - Drug Discovery Today
JF - Drug Discovery Today
IS - 6
ER -