The scientific evidence base for Sports & Deep Tissue Massage

The causes of mental and physical fatigue experienced by people with MS are complex, and likely to include neural, inflammatory, metabolic, and psychological factors. None of the currently available approaches offers long term relief, say the researchers. Previous research suggests that dark chocolate, containing between 70 and 85 per cent cocoa solids, is associated with an improvement in subjectively assessed fatigue in people with chronic fatigue syndrome (ME). Cocoa, like dark chocolate, is rich in flavonoids––substances found abundantly in fruit and vegetables and associated with anti-inflammatory properties. This prompted the researchers to see if it might also be worth exploring Cocoa potential in helping to tackle the fatigue associated with MS. They randomly assigned 40 adults recently diagnosed with the relapsing remitting form of MS and fatigue to drink a cup of either high flavonoid cocoa powder mixed with heated rice milk (19) or a low flavonoid version (21) every day for six weeks.  Participants were instructed to wait 30 minutes before taking any prescribed medication or eating or drinking anything else, but otherwise to stick to their usual diet.  Fatigue and fatigability–the speed with which mental and physical fatigue set in–were formally assessed before the start, at the mid-point, and at the end of the trial.  And participants also subjectively rated their fatigue on a scale of 1 to 10, at 10.00, 15.00, and 20.00 hours each day, and monitored their activity with a pedometer.  After six weeks there was a small improvement in fatigue in 11 of those drinking high flavonoid cocoa compared with eight of those drinking the low flavonoid version. Those drinking the high flavonoid version showed a 45 per cent improvement in subjectively assessed fatigue and an 80 per cent improvement in walking speed.  Although not objectively measured, pain symptoms also improved more in the high flavonoid group. If the findings are confirmed in larger studies, it may offer a simple dietary approach to a persistent and hard to treat symptom, which affects nine out of 10 people with MS, suggest the researchers. Reference https://jnnp.bmj.com/content/90/5/507

For a while there has been an assumed link between poor sleep and heart disease but it was not understood.  Now fresh evidence suggests that sleep regulates a mechanism that can help to protect arteries from hardening.  Which reinforces the notion that good quality sleep is important for cardiovascular health. Researches studied the development of atherosclerosis - the process through which plaques or fatty deposits build up inside arteries causing them to narrow and stiffen.  They discovered sleep disturbed mice:

• Developed larger plaques in their arteries than mice that slept well.
• Had higher amounts of circulating, inflammatory cells.
• Produced lower amounts of hypocretin - a brain hormone that controls wakefulness.

The standard theory of heart disease states that fatty foods cause the arteries to "clog up" and narrow, which is a major feature of cardiovascular disease.  Researchers have discovered that a lack of sleep seem to have more to do with hardening of the arteries (atherosclerosis) than a fatty diet. Not getting enough sleep on a regular basis can cause a buildup of plaque in the arteries, which causes them to stiffen and eventually close. Researchers at Massachusetts General Hospital now think that hardening of arteries has more to do with a "neuro-immune axis" linking sleep to the cardiovascular system.  Sleep helps regulate the production of inflammatory cells and maintain healthy blood vessels, and so it would follow that lack of sleep has the reverse effect. The researchers demonstrated the effect on a group of laboratory mice.  Although the cholesteral levels of sleep deprived ice remained the same, they developed larger arterial plaques and had double the number of inflammatory cells known to contribute to hardening of arteries. Reference Tall AR, Jelic S. How broken sleep promotes cardiovascular disease. Nature. 2019 Feb;566(7744):329-330