Key result
Psoriasis is linked to a ~28% higher absolute prevalence of ventricular dyssynchrony versus controls.
Why the study?
Is psoriasis associated with left ventricular dyssynchrony in patients with normal ejection fraction and narrow QRS?
Case-Control (n=100)
Is psoriasis associated with left ventricular dyssynchrony in patients with normal ejection fraction and narrow QRS?
Patients with psoriasis exhibit early signs of left ventricular systolic dyssynchrony and diastolic dysfunction despite having a normal ejection fraction and narrow QRS.
May indicate early cardiac involvement in psoriasis with preserved EF; leaves open whether dyssynchrony predicts events or warrants screening.
BACKGROUND: Psoriasis is an inflammatory disorder, which has been reported to be associated with cardiovascular (CV) risks. Although increased CV risks in psoriasis are well established, there are no data about changes of contraction synchrony in psoriasis. Therefore, we aimed to study the left ventricular (LV) contraction synchrony in patients with psoriasis with narrow QRS and normal ejection fraction. METHODS: Fifty patients with psoriasis and 50 age- and sex-matched control subjects were included in the study. LV dyssynchrony was investigated by color-coded tissue Doppler imaging. RESULTS: In the psoriasis group, the mean high-sensitive C-reactive protein values were significantly higher compared with the controls. Peak A velocity, deceleration time, isovolumetric relaxation time, and E/E' values were higher in the psoriasis group; however, E/A ratio and average Em were higher in the control group. LV systolic dyssynchrony parameters [including standard deviation of Ts of the 12 LV segments (Ts-SD-12), maximal difference in Ts between any two of the 12 LV segments, standard deviation of Ts of the six basal LV segments, and maximal difference in Ts between any two of the six basal LV segments] were found to be higher in the psoriasis group. The patients with ventricular dyssynchrony (a Ts-SD-12 >34.4 ms) were higher in the psoriasis group than the control group (34% vs. 6%, P < 0.01). CONCLUSION: In patients with psoriasis with normal ejection fractions and narrow QRS, LV systolic dyssynchrony is an early manifestation of heart involvement and may coexist with diastolic dysfunction.
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Şen et al. (2014) conducted a case-control in Psoriasis (n=100). Psoriasis vs. Age- and sex-matched control subjects was evaluated on Ventricular dyssynchrony (a Ts-SD-12 >34.4 ms) (p=< 0.01). Patients with psoriasis had a significantly higher prevalence of ventricular dyssynchrony compared to age- and sex-matched controls (34% vs. 6%, P < 0.01).
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