TY - JOUR
T1 - Clopidogrel and the risk of osteoporotic fractures
T2 - a nationwide cohort study
AU - Jørgensen, Niklas Rye
AU - Grove, Erik Lerkevang
AU - Schwarz, Peter
AU - Vestergaard, Peter
N1 - © 2012 The Association for the Publication of the Journal of Internal Medicine.
PY - 2012
Y1 - 2012
N2 - Objectives: The P2Y(12) inhibitor clopidogrel inhibits platelet aggregation and is used in the treatment and prevention of coronary artery disease. It is widely used and, in combination with acetylsalicylic acid, is the standard of care for acute coronary syndrome and percutaneous coronary intervention. The mode of action of clopidogrel involves pathways that are important to the metabolic activity in bone cells, although to our knowledge whether P2Y(12) receptors are involved in the regulation of bone metabolism has not yet been investigated. Therefore the objective of the present study was to investigate the association between clopidogrel use and risk of fractures. Methods: We investigated the association between clopidogrel use and fracture incidence in a nationwide cohort study within the Danish population of approximately 5.3 million individuals. All patients who were prescribed clopidogrel during the years 1996-2008 were included in the study (n=77,503) and three non-users were randomly selected, matched for age and gender (n=232,510), for each clopidogrel-treated subject. Results: Treatment with clopidogrel was associated with both increased overall fracture risk and increased risk of osteoporotic fractures, especially in subjects with a treatment duration of more than 1 year. However, individuals with low exposure to clopidogrel (
AB - Objectives: The P2Y(12) inhibitor clopidogrel inhibits platelet aggregation and is used in the treatment and prevention of coronary artery disease. It is widely used and, in combination with acetylsalicylic acid, is the standard of care for acute coronary syndrome and percutaneous coronary intervention. The mode of action of clopidogrel involves pathways that are important to the metabolic activity in bone cells, although to our knowledge whether P2Y(12) receptors are involved in the regulation of bone metabolism has not yet been investigated. Therefore the objective of the present study was to investigate the association between clopidogrel use and risk of fractures. Methods: We investigated the association between clopidogrel use and fracture incidence in a nationwide cohort study within the Danish population of approximately 5.3 million individuals. All patients who were prescribed clopidogrel during the years 1996-2008 were included in the study (n=77,503) and three non-users were randomly selected, matched for age and gender (n=232,510), for each clopidogrel-treated subject. Results: Treatment with clopidogrel was associated with both increased overall fracture risk and increased risk of osteoporotic fractures, especially in subjects with a treatment duration of more than 1 year. However, individuals with low exposure to clopidogrel (
U2 - 10.1111/j.1365-2796.2012.02535.x
DO - 10.1111/j.1365-2796.2012.02535.x
M3 - Journal article
C2 - 22372976
SN - 0954-6820
VL - 272/4
SP - 385
EP - 393
JO - Journal of Internal Medicine
JF - Journal of Internal Medicine
ER -