The interaction of pressure and duration of cupping therapy significantly modulated dynamic hemodynamic responses, including DeoxyHb myogenic wavelet power (p=0.046) and OxyHb sample entropy (p=0.029).
Does the interaction of pressure and duration in cupping therapy modulate the complexity and fractal properties of hemodynamic signals in healthy participants?
The interaction of pressure and duration during cupping therapy significantly modulates the complexity and fractal properties of microvascular hemodynamic responses.
Cupping therapy has been demonstrated to improve hemodynamic regulation. Existing studies have reported mean changes of oxyhemoglobin (OxyHb) and deoxyhemoglobin (DeoxyHb), which do not capture the multi-scale regulatory dynamics of the microvasculature. It is therefore unclear whether cupping therapy modulates the complexity and fractal property of hemodynamic signals. The objective of this study was to examine complexity of hemodynamic response to cupping therapy. A 2 by 2 factorial design with repeated measures was used to examine the main effect of pressure (−225 and −300 mmHg) and duration (5 and 10 min) and their interaction. A near infrared spectroscopy (NIRS) was used to measure OxyHb and DeoxyHb concentrations before and after cupping therapy. A total of 18 healthy participants were enrolled in this study. The wavelet analysis, sample entropy and detrended fluctuation analysis (DFA) were used to quantify the oscillatory, complexity, and fractal scaling properties of OxyHb and DeoxyHb signals. A two-way ANOVA with Bonferroni correction was used to examine the main and interaction effects. The results demonstrated that the combined effects of pressure and duration, rather than either factor independently, were the primary determinants of the dynamic hemodynamic response to cupping therapy, with significant Pressure × Duration interactions observed in DeoxyHb myogenic wavelet power (F = 4.636, p = 0.046, η2p = 0.214), OxyHb (F = 5.704, p = 0.029, η2p = 0.251) and DeoxyHb (F = 6.600, p = 0.020, η2p = 0.280) sample entropy, and DeoxyHb DFA scaling exponent (F = 5.598, p = 0.030, η2p = 0.248). In addition, cupping pressure selectively modulated neurogenic DeoxyHb oscillatory power (F = 5.001, p = 0.039, η2p = 0.227), and cupping duration significantly altered the fractal scaling properties of DeoxyHb signals (F = 7.775, p = 0.013, η2p = 0.314). The findings indicate that the interaction of pressure and duration of cupping therapy could effectively modulate hemodynamic responses. To the best of our knowledge, this is the first study investigating the complexity of hemodynamic responses after cupping therapy.
Dabirian et al. (Wed,) conducted a other in Healthy (n=18). Cupping therapy vs. Internal comparison (2x2 factorial design) was evaluated on Oscillatory, complexity, and fractal scaling properties of OxyHb and DeoxyHb signals. The interaction of pressure and duration of cupping therapy significantly modulated dynamic hemodynamic responses, including DeoxyHb myogenic wavelet power (p=0.046) and OxyHb sample entropy (p=0.029).