Aldosterone glucuronidation inhibition as a potential mechanism for arterial dysfunction associated with chronic celecoxib and diclofenac use in patients with rheumatoid arthritis

• Published in: Clinical and experimental rheumatology 2013-09, Vol.31 (5), p.691
• Main Authors: Crilly, Michael A, Mangoni, Arduino A, Knights, Kathleen M
• Format: Article
• Language: English
• Subjects: Adult; Aged; Aldosterone - metabolism; Anti-Inflammatory Agents, Non-Steroidal - adverse effects; Arthritis, Rheumatoid - drug therapy; Celecoxib; Cyclooxygenase 2 Inhibitors - adverse effects; Diclofenac - adverse effects; Female; Glucuronides - metabolism; Humans; Kidney Cortex - drug effects; Kidney Cortex - metabolism; Linear Models; Male; Microsomes; Middle Aged; Multivariate Analysis; Pulse Wave Analysis; Pyrazoles - adverse effects; Risk Factors; Sulfonamides - adverse effects; Vascular Diseases - chemically induced; Vascular Diseases - metabolism; Vascular Diseases - physiopathology; Vascular Stiffness - drug effects
• ISSN: 0392-856X

Adverse cardiovascular (CV) effects of non-steroidal anti-inflammatory drugs (NSAIDs) are largely independent of their cyclooxygenase (COX) enzyme selectivity, but could be a consequence of aldosterone 18ß-glucuronidation inhibition (AGI), which varies between NSAIDS. This study assesses the chronic effects of celecoxib (selective COX-2 inhibitor) versus diclofenac (non-selective NSAID) therapy on arterial dysfunction in patients with rheumatoid arthritis (RA). AGI was assessed in vitro using human kidney cortical microsomes. Arterial function was measured clinically as the extent (augmentation index, AIX%) and timing (reflected wave transit time, RWTT, msec) of arterial wave reflection using radial applanation pulse wave analysis (SphygmoCor PWA device) in 39 RA patients without overt CV disease aged 40-65. A higher AIX% (and lower RWTT) indicates arterial dysfunction. Clinical assessment on a single occasion included a fasting blood sample, patient questionnaire and medical record review. Multivariable analysis was used to adjust for sex, mean blood pressure, arthritis duration, cumulative ESR-years and current DMARD therapy. The inhibition constant (Ki) for celecoxib was lower than that of diclofenac (Ki, 3.5 vs. 8.4 μM). Chronic celecoxib use was associated with a higher AIX% (34.8 vs. 32.3) and lower RWTT (130.1 vs. 132.7 msec) compared with diclofenac. Adjusted mean differences were AIX% 4.7 (95%CI 0.6 to 8.9; p=0.03) and RWTT -3.6 (95%CI -10.0 to 2.7; p=0.26). Celecoxib has a greater potency for AGI than diclofenac and its use is associated with a significantly higher AIX%. Our findings support AGI as a plausible mechanism for the CV toxicity of NSAIDs.