Pressure Mounting: Is Fibromyalgia Caused By High Pressure in the Brain (Intracranial Hypertension)


We propose that chronic idiopathic CSP dysregulation underlies both FM and the clinical entity of STC, which both present as peripheral neurological disorders. The authors

This is the third in a series of blogs providing overviews of new hypotheses for fibromyalgia and chronic fatigue syndrome (FM, ME/CFS). (It is also part I of a three part head and neck series on fibromaylgia and ME/CFS).

Whoever ends up explaining fibromyalgia is going to have to explain the wide variety of symptoms found in it. A group from Belgium – a country not particularly known for its biological interpretations of diseases like chronic fatigue syndrome – believes that FM patent’s brains and spinal cord are under too much pressure.

Fibromyalgia and unexplained widespread pain: The idiopathic cerebrospinal pressure dysregulation hypothesis. M. Hulensa,⁎, W. Dankaertsa, I. Stalmansb,c, A. Somersb,c, G. Vansantd, R. Rasschaerte, Bruyninck  2018 Jan;110:150-154. doi: 10.1016/j.mehy.2017.12.006. Epub 2017 Dec 5.

Tight Sleeves

More specifically this group believes that high spinal fluid pressure in the sleeves of the spinal nerve roots of FM patients is compressing those nerves causing a “polyradiculopathy” or pinched sensory nerves across the spine. These pinched sensory nerves are in turn causing pain and other symptoms across the body.  The difference between these pinched nerves and the pinched nerves we ordinarily think of is that spinal fluid pressure, not structural problems, are the cause.

Is fluid buildup in the nerve roots of the spinal cord causing symptoms in fibromyalgia?

Certainly something is going on in the head and upper bodies of FM patients. Upper body pain, feelings of pressure in the head and head pain are common. The researchers argued that the peripheral neuropathy (numbness, tingling, electric shocks, burning sensations, allodynia, weakness) and reduced muscle strength studies have found could all be caused by increased spinal fluid pressure.

Interestingly, they propose that the deep muscle pain FM patients sometimes feel could be due to damaged and/or lost small nerve fibers in their sensory nerves. (Dr. Oaklander has also proposed that small nerve loss inside the body may be causing many symptoms in FM.)  They believe that high levels of pressure are causing degeneration of the sensory nerve roots. Nerve conduction studies showing demyelination is present in some FM patients buttress, they say, that finding.

The authors also propose that the gastrointestinal problems so common in fibromyalgia could be caused by compression of the nerves in the lower spine.

Fibromyalgia Mimics

They note that similar symptoms to FM (upper body pain, facial pain, cognitive problems, gait issues, reduced gray matter volume and others) also occur in several diseases associated with increased cerebral spinal pressure (Idiopathic intracranial hypertension (IIH) and Idiopathic normal pressure hydrocephalus (INPH).

Tarlov Cysts

High spinal fluid pressure may be causing Tarlov cysts as well. Tarlov cysts are cerebrospinal fluid filled sacs which form inside of the sheaths surrounding the dorsal root ganglion’s nerve roots. (The dorsal root ganglion are clusters of nerve cell bodies found in nerves emanating from the spinal cord. They convey sensory and other information to the spinal cord.)

The authors believe Tarlov cysts provide a kind of buffer for the sensory nerves against the increased cerebral spinal fluid pressure emanating from the spinal cord.  (Tarlov cysts are also believed to result from inflammation, trauma or disease).

When small these cysts often cause no symptoms, but when they  are larger they can, by putting pressure on the sensory nerves, cause pain, tingling, muscle spasms,  muscle problems, and/or pinched nerves. For some reason women are more likely to suffer from them.

A Chronic Fatigue Syndrome (ME/CFS) Connection?

The cerebral spinal fluid fibromyalgia hypothesis is interesting given the small 2013 chronic fatigue syndrome (ME/CFS) study suggesting that high intracranial pressure and headaches are common in people with ME/CFS.

Twenty percent of the 20 study participants meet the international criteria for idiopathic  intracranial hypertension (IIH) and were reclassified as having that condition and were treated.  Even more interesting were the 85% of ME/CFS patients who, without having high spinal fluid pressures, nevertheless benefited from reductions in spinal fluid pressure.

questions - cerebral spinal fluid test results ME/CFS

Do the normative values of cerebral spinal fluid tests apply in ME/CFS/FM?

None of the responders had the major clinical signs (papilloedema, visual disturbances) doctors look for to suspect IIH. When their spinal fluid pressure was reduced they reacted just like IIH patients do – they felt better; i.e. they experienced reduced headaches, heightened alertness and reduced  atigue that lasted anywhere from a couple of minutes to several weeks.

Dr Higgins concluded that the normative values for IIH are probably incorrect and that some people, perhaps many people, suffer from IIH at far lower cerebral pressures than is currently expected. They also display different symptoms (little eye involvement) from traditional IIH patients.

In a recent blog ME/CFS/FM/POTS/EDS patient Caroline Christian reported that her Stanford neurologist suspected she was suffering from spontaneous leaks of spinal fluid and “pseudomotor cerebri” or excess cerebral spinal fluid and increased cerebral spinal fluid blood pressure. People with this condition usually have worsening head pain when their head is slightly lower than their body.  Dull headaches, often at the back of the head and worse at night or first thing in the morning are common.  The increased pressure can produce temporary problems with blurred vision or even blindness and double vision.

Personally, Dr. Higgin’s study and the FM hypothesis brought to mind a spinal tap which left me feeling unusually relaxed and clear for a couple of hours. I also know of a person who’s ME/CFS/POTS virtually disappeared for two weeks following a spinal tap. A Canadian doctor is reportedly working on a paper highlighting the unusual changes she sometimes sees in her ME/CFS/FM patients after spinal taps.

Assessing Cerebral Spinal Fluid Pressures

Unfortunately, assessing cerebral spinal fluid pressure is not easy (it usually requires a spinal tap). Plus as we’ve seen, normative CSF pressure values may not be very normative in ME/CF/FMS and some people with seemingly normal CSF values can benefit significantly from a reduction in pressure.

The authors of the article suggested that the following tests be done to assess the presence of high intracranial pressure: spinal tap, sensory testing using a pin-prick test, strength testing, knee and Achilles tendon reflexes, a tandem gait test, a revision of the MRI to detect possible nerve root dilations and TCs, NCS/EMG, and measurement of the retinal nerve layer thickness using an optical microscope.


Treatment for increased cerebral spinal fluid pressure usually consists of carbonic anhydrase inhibitors (such as acetazolamide (Diamox), Methazolamide (Neptazane), furosemide (Lasix) and topiramate (Topamax)) which reduce CSF levels.

Acetazolamide or Diamox, the most commonly used drug to treat IIH, is used to treat altitude sickness, glaucoma, water retention, non-glaucoma associated eye pressure, seizures, epilepsy and others.

The Intracranial Hypertension Research Foundation reports that spinal fluid pressure rises when the body can no longer effectively absorb or drain it. Ray Perrin has some ideas about that – his work will form the second part of HR’s FM and ME/CFS Head and Neck Series.

Health Rising’s Fibromyalgia and ME/CFS Head and Neck Series

  • Pt. I – Pressure Mounting: Is Fibromyalgia Caused By High Pressure in the Brain (Intracranial Hypertension)
  • Pt. II – Ray Perrin – Reduced Lymphatic Drainage in ME/CFS/FM
  • Pt II – Dr. Rowe – Spinal stenosis and ME/CFS



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Cort Johnson

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About MafibromaVie 5996 Articles
Bonjour, je n'ai même pas encore 40 ans, je suis fibromyalgique, j'ai un petit garçon de 2 ans, et je vis dans cette souffrance, mais dû a ma personnalité je ne peux pas rester sans rien faire, car ça me tue encore plus que la douleur. Je précise que j’écris le français que a 5 ou presque 6 ans maintenant et je parle et écris aussi d'autres langues, donc je fais des erreurs de orthographe et de grammaire. Le problème c'est que je ne peux presque plus marcher (béquilles et difficile), être assis durant plus de 15 à 30 minutes ça me tue le cul cul et le dos, même pour soulever mon petit qui pèse a peine 12 kg, mais on dirait un sac de ciment du type 50 kg. Lui changer la couche me fait trembler les jambes et on dirait qu'on me plante un couteau au fond du dos, même mes épaules et bras quand je soulève ces fesses me font mal, même quand je lui donne la soupe avec une petite cuiller mon bras se fatigue vite et les douleurs arrivent, L'autre jour on lui donnant la soupe j'ai appuyé mon bras sur le plateau de ça chaise et il a commencé à trembler violemment, que même mon petit de 2 ans a eu peur. Sur ma page j'assume l'identité de tous les fibromyalgiques du moins de ceux qui veulent me suivre sous le pseudonyme de "MafibromaVie" ou de "FiFi le clown", finalement nous sommes tous des Clows au yeux de trop de gens, d’État, de Pays, et de Communauté dans notre cas la UE! Je ne suis pas une personnalité et je ne recherche aucune reconnaissance publique. Je suis simplement une personne comme toutes les autres, comme vous qui souffrait peut être aussi de Fibromyalgie, et qui a ouvert une simple page privée ou j'ecris ma vie de fibromyalgique pour suivie médicale par mon médecin. Ben après avec le temps, l'histoire a changé beaucoup de monde a commencer a me suivre 50,100,1000 et maintenant plus de 3000. Je parlais plus de moi au début et maintenant plus de nous et pour vous, ainsi c'est crée une page de partage, aide, soutien, et de discussion pour tous les fibros.

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