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Diastolic Dysfunction of the Left and Right Ventricles in Patients with Calcium Pyrophosphate Crystal Storage Disease
M S Eliseev1, O V Zhelyabina2, I G Kirillova1
1Nasonova Research Institute of Rheumatology, Moscow, Russia.
Insights
Diastolic dysfunction (DD) is common in patients with calcium pyrophosphate crystal deposition disease (CPPD) and osteoarthritis (OA). DD in CPPD is linked to low vitamin D, while in OA it
Area of Science:
- Cardiology
- Rheumatology
- Medical Imaging
Background:
- Diastolic dysfunction (DD) prevalence and risk factors in patients with calcium pyrophosphate crystal deposition disease (CPPD) and osteoarthritis (OA) are understudied.
- Understanding DD in these patient groups is crucial for cardiovascular risk assessment and management.
Purpose of the Study:
- To determine the frequency of left ventricular (LV) and right ventricular (RV) DD in patients with CPPD and knee OA.
- To identify risk factors associated with the development of DD in these patient populations.
Main Methods:
- A study cohort of 26 patients with CPPD and knee OA (aged 18-65) without cardiovascular disease, type 2 diabetes, or other rheumatic diseases was analyzed.
- Conventional cardiovascular risk factors were assessed, and echocardiography was performed to evaluate LV and RV function.
- Statistical analyses were used to compare DD prevalence, risk factors, and echocardiographic parameters between the CPPD and OA groups.
Main Results:
- A high frequency of DD was observed in both CPPD (42%) and OA (31%) groups, with no significant difference between them.
- Type 1 DD was the predominant form, affecting both LV and RV. No types 2 or 3 DD were detected.
- In CPPD patients, DD correlated with lower vitamin D levels. In OA patients, DD was associated with higher serum uric acid (sUA) and lower parathyroid hormone (PTH) levels.
Conclusions:
- There is a high prevalence of LV and RV diastolic dysfunction in patients with CPPD and OA.
- Specific risk factors for DD differ between CPPD (low vitamin D) and OA (high sUA, low PTH).
- These findings highlight the importance of cardiac evaluation in patients with CPPD and OA.
Abstract:
The frequency and risk factors for the development of diastolic dysfunction (DD) in patients with CPPD and OA have not been studied. The objective of this study was to determine the frequency and identify risk factors (RF) for the development of DD of the left and right ventricles (LV and RV) in patients with calcium pyrophosphate crystal deposition disease (CPPD) and osteoarthritis (OA). The study included 26 patients with CPPD and with knee OA 18-65 years old, matched in age and gender, without cardiovascular disease (CVD), type 2 diabetes mellitus (DM2), and rheumatic diseases. Conventional risk factors (TRF) of CVD were assessed, and echocardiography was performed. The frequency of DD in patients with CPPD and OA was quite high and almost did not differ in both groups: it was detected in 19 patients, of which 11 (42%) had CPPD and 8 (31%) had OA (p = 0.39). Type 1 LV DD was detected in 10 (39%) patients with CPPD and in 8 (31%) with OA (p = 0.11); type 1RV DD was detected in 8 (31%) patients with CPPD and in 7 (27%) patients with OA (p = 0.17); and type 1 LV DD and RV DD was detected in 7 (27%) patients with both CPPD and with OA. DD types 2 and 3 were not detected in both groups. There were no differences in both groups in CV risk factors, except for the level of CRP (it was higher in CPPD) (p = 0.03). In the CPPD group, mean values of LV E/E' (p = 0.02), LVDT (p = 0.03), LVMI (p = 0.04) were significantly higher than in patients with OA. On the contrary, in patients with OA, indices EDV (p = 0.004) and TVC (p = 0.02) were higher. There were direct correlations between diastolic function indices and the following factors in CPPD: LVL, PWLV and PTH level (r = 0.7, p <0.005), LV E' and PTH level (r = 0.7, p < 0.005). Inverse correlations were found between the level of PTH and IS (r = -0.5, p < 0.005), LVMI (r = -0.5, p < 0.005), and the level of vitamin D and VDDT (r = -0.6, p < 0.005). Direct correlations in OA were found between the level of CRP and PVAdiast (r = 0.6, p < 0.005), and the level of sUA (r = 0.7, p < 0.005), and the level of vitamin D and E/E'LV (r = 0.6, p < 0.005). A high prevalence of LV and RV DD was found in patients with CPPD and OA. The presence of DD in CPPD was associated with lower vitamin D levels, and in OA with a higher level of sUA and a lower level of PTH.
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