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Pulse abnormalities at rest and during tilt test could be highly indicative screen for ME/CFS
Saturday 4 February 2012
By John Allen, et al.
[Note: To read the full text of this article free, click here. The best-known sign of orthostatic intolerance involves symptoms (e.g., weakness, faintness) in an upright position that can be relieved by lying prone.]
The frequent finding of autonomic dysfunction and symptoms on standing has the potential to provide a diagnostic biomarker in chronic fatigue.
In this study we explored the clinical value of non-invasive optical multi-site photoplethysmography (PPG) technology to assess cardiovascular responses to standing. [PPG is a quick, low-cost measurement of changes in pulsed skin blood volume using a small light probe that is placed on the surface of the skin.]
Multi-site PPG pulses were collected from tissue pads of the ears, fingers and toes of 14 patients with CFS and 14 age-matched sedentary subjects using a measurement protocol of a 10 min baseline (subject supine) followed by 3 min of tilting on a tilt table (head-up to 70 degrees).
Percentage change in pulse timing (pulse transit time, PTTf) and pulse amplitude (AMP) at each site were calculated using beat-to-beat pulse wave analysis.
A significant reduction in the overall pulse timing response to controlled standing was found for the CFS group (using summed absolute percentage change in pulse timing for ear, finger and toe sites, median change of 26% for CFS and 37% for control with p = 0.002).
There were no significant differences between subject groups for the pulse amplitude measure at any site. Changes in pulse amplitude with tilt were, however, weakly significantly and negatively correlated with fatigue severity (p < 0.05).
Receiver operating characteristic (ROC) analysis of timing measures produced an area under the curve of 0.81. Experimental linear discriminant classification analysis comparing both timing and amplitude measures produced an overall diagnostic accuracy of 82%.
Pulse wave abnormalities have been observed in CFS and represent a potential objective measure to help differentiate between CFS patients and healthy controls.
Source: Physiological Measurement, Jan 25, 2012. PMID:22273713, by Allen J, Murray A, Di Maria C, Newton JL. Microvascular Diagnostics, Regional Medical Physics Department, Freeman Hospital, Newcastle upon Tyne; UK NIHR Biomedical Research Centre in Ageing and Age-Related Diseases, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, UK. [Email: Julia.firstname.lastname@example.org]
The above originally appeared here.
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