Incidence and risk factors of venous thromboembolism in ANCA-associated vasculitis: a metaanalysis and metaregression

Clinical Rheumatology - The incidence of venous thromboembolism (VTE) in ANCA-associated vasculitis patients varies in different populations. Moreover, the risk factors for VTE in these patients...     

Risk of coronary artery disease in patients with systemic sclerosis: a systematic review and meta-analysis

Several chronic inflammatory disorders, such as rheumatoid arthritis and systemic lupus erythematosus, have been shown to increase coronary artery disease (CAD) risk but the data on systemic sclerosis (SSc) is unclear. We conducted a systematic review and meta-analysis of observational studies that reported odds ratio, relative risk, hazard ratio, or standardized incidence ratio comparing CAD risk in patients with SSc versus non-SSc participants. Pooled risk ratio and 95 % confidence intervals were calculated using a random effect, generic inverse variance method. Four studies were identified and included in our data analysis. The pooled risk ratio of CAD in patients with SSc was 1.82 (95 % CI, 1.40 to 2.36). The statistical heterogeneity of this meta-analysis was moderate with an I ² of 73 %. Our study demonstrated a statistically significant increased CAD risk among patients with SSc.     

Elevated admission serum calcium phosphate product as an independent risk factor for acute kidney injury in hospitalized patients

Background: Increased serum calcium-phosphate product (CaP) can result in acute kidney injury (AKI) due to tubular and interstitial calcium phosphate deposits. CaP of > 55 mg²/dL² is also associated with systemic calcification. However, the risk of AKI development among hospitalized patients with different admission calcium-phosphate product levels remains unclear.

Methods: All adult hospitalized patients who had both admission serum calcium and phosphate levels available from 2009 through 2013 were enrolled. Admission CaP was categorized based on its distribution into six groups (<22, 22- < 27, 27- < 32, 32- < 37, 37- < 42 and ≥42 mg²/dL²). The odds ratio (OR) of in-hospital mortality by admission CaP, using the CaP category of < 22 mg²/dL² as the reference group, was obtained by logistic regression analysis.

Results: After excluding patients with end-stage renal disease, without serum creatinine measurement, and those who presented with AKI at the time of admission, a total of 9,864 patients were studied. In-hospital AKI occurred in 1,478 patients (15.0%). The incidence of AKI among patients with admission CaP < 22, 22 to < 27, 27 to < 32, 32 to < 37, 37 to < 42, and ≥42 mg²/dL² was 11.1%, 12.4%, 14.9%, 15.2%, 17.5%, and 19.9%, respectively. After adjusting for potential confounders, a CaP ≥37 mg²/dL² was associated with an increased risk of developing AKI with OR of 1.53 (CI 1.19–1.96) and 1.63 (CI 1.25–2.14) in patients with admission CaP 37- < 42 and ≥42, respectively. Subgroup analysis based on eGFR consistently demonstrated that CaP ≥37 mg²/dL² was associated with an increased risk of developing AKI in both chronic kidney disease (CKD) and non-CKD patients.

Conclusion: Elevated admission CaP was independently associated with an increased risk for in-hospital AKI.