A 45 year old male recently presented to my practice. He
suffered with a progressive, debilitating, multisystem disease over a period of
5 years. An MRI of the brain was performed and the results were unnerving. The
scan showed numerous white matter lesions, greater than 20. The diagnosis of
MS was suggested by the radiologist.
Mainstream authorities all agree: There is no diagnostic
test for MS. The diagnosis can only be made when other causes of the symptoms
and findings have been ruled out. It is a diagnosis of exclusion. MRI
protocols, proteins in the spinal fluid, abnormal evoked potentials, alone or
in combination cannot conclusively make the diagnosis the MS.
This patient lives in a Lyme endemic area and has had
numerous tick bites over a period of many years. He suffers with fatigue, weakness,
trouble walking, poor endurance, headaches, cognitive symptoms and memory loss,
depression, tinnitus, night sweats, flulike symptoms, migratory joint pain,
mood swings and episodes of rage.
The left lower extremity was particularly weak showing a
“foot drop,” apparent with gait testing. The patient was instructed to walk on
his heels but the left foot is unable to elevate and the foot flops to the
floor. An EMG showed the cause to be inflammation of the peroneal nerve, a
peripheral nerve. This is not a feature of MS which involves only the central
nervous system. Lyme, however, effects all aspects of the nervous system.
White matter lesions in the brain reflect damage of heavily
myelinated nerve fibers in the deep portions of the brain. Myelin is a white,
fatty, insulating substance which covers these neurons. Some nerve cells are
not covered by myelin, for example, those covering the top of the brain. These
nerve cells have a gray appearance hence the cortex (outer surface) of the
brain, is composed of gray matter.
White matter lesions can have many causes. They can be
normal; you are allowed one per decade of life. The lesions may be seen with
atherosclerosis, diabetes causing small blood vessel disease, hypertension,
migraines, infections, vasculitis and Lyme disease and there are many other
potential causes listed in texts and various sources.
Multiple sclerosis is characterized as a demyelinating
disease. It results from an autoimmune process which attacks this coating of
the deep nerve cells. MS is divided into 4 types. In 85% of cases it is
relapsing and remitting. Patients have discrete neurological events (central
nervous system only) which generally get better over time. MS is not diagnosed
based on a single event. Subsequent events occur over time involving different
parts of the central nervous system.
Typical “events” may include: optic neuritis with loss of
vision; weakness, generally localized; numbness and shooting pains originating
from the central nervous system, vertigo and loss of bowel and/or bladder
function. In most cases patients get
better. Interim periods of time, devoid of symptoms, are followed recurring events causing
different symptoms. Over time, the symptoms may not remit and become permanent.
These events are dramatic and distinct. MS is a disease of
fits and starts.
The Multiple Sclerosis Society states common symptoms of MS
include: fatigue, trouble walking, numbness and tingling, weakness, changes in
vision, changes in bowel and bladder function, changes in cognition, depression
and pain. The National Multiple Sclerosis Society states that one half of MS
patients end up with a chronic pain syndrome. By my way of thinking, the
recognition of such symptoms after the fact speaks to a more insidious, gradual
inflammatory brain disorder and a multisystem disorder more characteristic of
late Lyme disease. Why has the disease morphed?
MS is not defined by MRI findings. In the case of the above
mentioned patient, there is a history of tick bite, positive Lyme test and
evidence of a progressive, multisystem disease. These white matter lesions, numerous as they are, are
most likely the results of Lyme, neuroborreliosis.
The cause(s) of MS are thought to be both genetic and environmental
(including infection).
MS has an interesting epidemiology. Cases are rare around
the equator. The incidence increases proportionally to the distance one is away
from the equator. For example, it is more prevalent in the Northern U.S. and
Candida and Northern Europe and Scandinavia. The rule does not hold true for
the Asian continent where the incidence remains relatively low throughout the
continent. Sporadic epidemics of MS have been described, suggesting an unknown,
probably viral, infectious cause. Chamydia pneumonia has been shown to be the
culprit in some cases. Coincidently, there is a lot of overlap between the
geographic distribution of MS and Lyme.
The MS Society has a clear opinion about Lyme: it is not
associated with MS. It is easy for the Society to make this claim: they follow
the IDSA approach. Lyme responds to 3 weeks of antibiotics. White matter
lesions in a previously treated Lyme patient are therefore the result of MS,
not Lyme.
How Lyme causes these lesions is not entirely clear. It has
been proposed that the highly immuno-inflammatory proteins expressed on the
surface of Lyme spirochetes may evoke an autoimmune reaction, one that has not
yet been categorized. This raises the question: are some forms of neuro-Lyme a
type of MS or a close relative? Can Lyme cause MS?
This is a murky arena. A subset of patients may respond best
to MS therapy combined with Lyme therapy. Perhaps some patients do have both
Lyme and MS.
There exist 10 FDA approved drugs for the long term
management of MS. Some suppress the immune system, like drugs used by
rheumatologist for rheumatoid arthritis. Others modulate immune responses and
others have anti-viral properties. Neurologist typically treat acute flares of
disease with high doses of intravenous steroids. Many of my patients got worse when given steroids. When patients have Lyme (and
are also treated by neurologists for MS) I like to steer them to immune
modulating and antiviral therapy (interferon).
Clearly, MS is a real disease, apart from Lyme. Not all MS
is caused by Lyme. However, there seems to be a large universe of patients
suffering with Lyme disease who have been incorrectly diagnosed with MS.
P.S. After only a month of oral doxycycline the patient has
experienced dramatic improvements in many symptoms.
Hi Doc:
ReplyDeleteNice post on MS. On a related point you may want to visit Dr. Terry Wahls, MD web site. She is a MD who came down with MS and through diet and medications was able to restore her health.
Thanks again for your informative posts.
Hi. doc!
ReplyDeleteYou write:"it is more prevalent in the Northern U.S. and Candida and Northern Europe and Scandinavia."
I think it should be
"it is more prevalent in the Northern U.S. and CANADA and Northern Europe and Scandinavia.
I love your blog!
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Interresting. So doxy works, why dont we start with this in early m.s.?
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