On Sunday, December 8th, I wrote my first blog
post about Grain Brain, by David Perlmutter, MD. It covered the introduction and 1st
chapter of the book. This post covers
chapter two of the book titled: The Sticky
Protein – Gluten’s role in Brain Inflammation.
As a reminder, I have decided to blog about this book for two reasons: 1) to make the information stick in my own
brain; 2) to hear your comments. Please
leave comments and let me know your thoughts.
I welcome a lively discussion on the thoughts presented in my blog posts. If you decide to read the
book, I’d be very interested to know what you think of it.
Chapter 2 of Grain Brain is focused on the discussion
of gluten and the role it plays in celiac disease and a variety of brain
disorders. The chapter starts with stories about three of Parlmutter’s patients; one suffered from persistent migraines, one
suffered from bipolar disorder, and one suffered from involuntary movement and
learning disorders. After listening to
all three of these patients’ complaints, Perlmutter tested each of them for
gluten sensitivity, all with positive results.
All three of the patients went on gluten free diets and all three
improved dramatically as a result.
Perlmutter states that these cases reflect a pattern that he has
witnessed in many of his patients.
Patients come into his office complaining of vastly different symptoms
and ailments that are often alleviated by removing gluten from the diet. He states, “It is my belief that gluten is a
modern poison, and that the research is compelling doctors like me to notice
and re-examine the bigger picture when it comes to brain disorders and
disease.”
Perlmutter describes gluten as a protein composite that acts
as the ‘glue’ that holds flour together to make bread products. Gluten can be found in many grains such as wheat
(most common source in the USA), rye, barley, spelt, kamut, and bulger. In addition, gluten can be found in many
other common household items; from cheese spreads to mascara to hair
conditioners.
While many people are aware of celiac disease they may not
know that there is a big difference between gluten
sensitivity and celiac disease; the latter is an extreme manifestation of the former. Celiac disease is basically
a severe allergic reaction to gluten that causes damage specifically to the
small intestine. While celiac disease is
the most recognized and most severe form of gluten sensitivity, gluten
sensitivity can impact any organ in the body.
Perlmutter explains that food sensitivities (not just gluten
sensitivity) are usually a response from the immune system. They also occur when the body doesn’t have
the right enzymes to break down a certain food.
He states that, “In the case of gluten, its ‘sticky’ attribute
interferes with the breakdown and absorption of nutrients. Poorly digested food leads to a pasty residue
in your gut, which alerts the immune system to leap into action, eventually
resulting in an assault on the lining of the small intestine.” But Perlmutter stresses, over and over again,
that even if you don’t experience typical digestive issues related to gluten
sensitivity, gluten sensitivity could lead to attacks elsewhere in your body, such as the
nervous system. When we negatively react
to food, our body “attempts to control the damage by sending out inflammatory
chemicals, killer cells among them, to wipe out the enemies.”
Occasionally, the books technical language caused me to have
a little trouble absorbing the message. When
I read the next several paragraphs I got hung up because I did not know the
exact definition of some words, so I looked them up and am providing you with
the definitions here:
antigen
noun
1. Immunology. Any substance that can stimulate the production of antibodies and combine specifically with them.
2. Pharmacology. Any commercial substance that, when injected of absorbed into animal tissues, stimulates the production of antibodies.
antigen
noun
1. Immunology. Any substance that can stimulate the production of antibodies and combine specifically with them.
2. Pharmacology. Any commercial substance that, when injected of absorbed into animal tissues, stimulates the production of antibodies.
cytokine
Any of several regulatory proteins, such as the interleukins and lymphokines, that are released by cells of the immune system and act as intercellular mediators in the generation of an immune response. Also called chemokine .
gliadin
noun Biochemistry .
1. a prolamin
derived from the gluten of grain, as wheat or rye,
used chiefly as
a nutrient in high-protein diets.
2. any prolamin.
prolamin
noun Biochemistry .
any of
the class of simple
proteins, as gliadin, hordein, or zein, found in grains,
soluble in dilute acids, alkalis, and alcohols, and insoluble in water, neutral
salt solutions, and absolute alcohol.
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Perlmutter wants the reader to understand how a sensitivity to
gluten can impact the brain, so he explains the following:
Prolamins are a class of simple proteins which are soluble
in dilute acids, alkalis, and alcohols but are not soluble in water and neutral
salt solutions. Gliadin is a prolamin
specific to gluten. Gluten sensitivity
is caused by an elevated immune system response to gliadin. Inflammation, which is the cornerstone of
many brain disorders, can be initiated by this immune system response. As the inflammation cycle evolves, cytokine chemicals,
which are antagonistic towards the brain, are released and collected and can
attack the brain. This process can
damage brain tissue and leave the brain vulnerable to dysfunction and disease,
particularly if the damaging conditions persist over a period of time. Elevated cytokines are seen in Alzheimer’s
disease, Parkinson’s disease, multiple sclerosis, and autism. 99% of the people whose immune systems react
negatively to gluten don’t know it.
Perlmutter likes a conclusion that Professor Marios Hadjivassiliou
(one of the most well-respected researchers in the area of gluten sensitivity
and the brain at the Royal Hallamshire Hospital in Sheffield) draws in a 1996
article published in Lancet, “Our
data suggest that gluten sensitivity is common in patients with neurological
disease of unknown cause and may have etiological significance.” (Definition:
Etiological: Of or pertaining to
causes or origins).
Perlmutter writes the following: “Dr. Hadjivassiliou goes on to state that ‘gluten
sensitivity can be primarily, and at times, exclusively, a neurological
disease.’ In other words, people with gluten sensitivity can have
issues with brain function without having any gastrointestinal problems
whatsoever.” For this reason,
Perlmutter tests all of his patients who have unexplained neurological
disorders for gluten sensitivity. Perlmutter
states, “I love how Dr. Hadjivassiliou and his colleagues stated the facts in a
2002 editorial in the Journal of Neurology,
Neurosurgery, and Psychiatry titled ‘Gluten Sensitivity as a Neurological
Illness’:
‘It has taken nearly 2,000 years to
appreciate that a common dietary protein introduced to the human diet
relatively late in evolutionary terms (some 10,000 years ago), can produce
human disease not only of the gut but also the skin and the nervous
system. The protean neurological manifestations
of gluten sensitivity can occur without gut involvement and neurologists must
therefore become familiar with the common neurological presentations and means
of diagnosis of this disease.’”
(Definition: Protean: readily assuming different forms or
characters; extremely variable.)
The editorial went on to state, ‘Gluten sensitivity is best
defined as a state of heightened immunological responsiveness in genetically
susceptible people. This definition does
not imply bowel involvement. That gluten
sensitivity is regarded as principally a disease of the small bowel is a
historical misconception.’
After Perlmutter concludes this rather scientific discussion
of gluten sensitivity, he summarizes the history of the discussion of celiac
disease and when gluten was finally linked to celiac and finally, to brain
dysfunction. The term celiac was first
introduced in the 1st century AD by Aretaeus of Cappadocia, a distinguished
ancient Greek doctor. There is evidence
of the discussion of celiac disease throughout medical literature since then,
with Dutch pediatrician Dr. Willem Karel Dicke finally linking celiac to gluten as a result of the Dutch famine of 1944.
During the famine bread and flour were scarce. Dr. Dicke noticed that celiac disease all but
disappeared in children, when it had been a fairly common problem before the famine. Dr. Dicke reports that after the famine, celiac
rates rose again, with mortality rates returning to original rates. About a century ago, the first anecdotal
reports began to emerge, in which doctors documented neurological disease in
patients with celiac. At that time, they
attributed the neurological problems to a nutrient deficiency caused by the
inability to digest food properly, not the brain’s reaction to a gluten
sensitivity. The turn-around, connecting
gluten sensitivity directly to neurological disease, is very recent. In 2006, the Mayo Clinic came out with a
report in the Archives of Neurology with a conclusion that was a “game-changer”
according to Perlmutter. It reads, “A
possible association exists between progressive cognitive impairment and celiac
disease, given the temporal relationship and the relatively high frequency of
ataxia and peripheral neuropathy, more commonly associated with celiac disease.” (Ataxia:
the inability to control voluntary muscle movements and maintain
balance, most frequently resulting from disorders of the brain. Peripheral neuropathy: nerve damage that encompasses a wide range of
disorders in which the damaged nerves outside of the brain and spinal cord
cause numbness, weakness and pain.)
The study that led to the above stated conclusion included 13
patients who showed progressive cognitive decline within two years of the onset
of celiac disease (anyone whose cognitive decline could be pinned on a possible
alternate cause was excluded from the study).
Two things of significance were noted among these patients, cognitive
decline could not be attributed to nutritional deficiencies and the patients
were relatively young to have dementia (median age 64; age range was 45 – 79).
Dr. Joseph Murray, a gastroenterologist and the study
investigator wrote; “There has been a fair amount written before about celiac
disease and neurological issues like peripheral neuropathy…or balance problems,
but this degree of brain problem – the cognitive decline we’ve found here – has
not been recognized before. I was not
expecting there would be so many celiac disease patients with cognitive
decline.” He reflected that it was
unlikely that these patients’ conditions reflected a “chance connection.” One of the findings of the study was that
patients who were put on a gluten-free diet experienced “significant
improvement” in their cognitive decline.
In this report, Dr. Murray mentioned the possible link between brain
impairment and inflammatory cytokines.
When participants in the study stopped consumption of
gluten, their brain scans revealed noticeable changes in the white matter on
the brain that could easily be confused with multiple sclerosis or small strokes.
Dr. Perlmutter notes, “This is the reason I always
check for gluten sensitivity in patients referred to me with a diagnosis of
multiple sclerosis; on many occasions I’ve found patients whose brain changes
were in fact not related to multiple sclerosis at all and were likely due to
gluten sensitivity. And lucky for them,
a gluten-free diet reversed their condition.”
Towards the end of Chapter 2, Perlmutter sites yet another article, this one written by
Dr. Rodney Ford of the Children’s Gastroenterology and Allergy Clinic in New
Zealand, published in 2009 titled, “The Gluten Syndrome: A Neurological Disease:” The article states: “The
fundamental problem with gluten is its’ interference with the body’s neural
networks…gluten is linked to neurological harm in patients, both with and
without evidence of celiac disease.”
Ford added, “Evidence points to the nervous system as the primary site
of gluten damage,” he concluded that, “the
implication of gluten causing neurological network damage is immense. With estimates that at least one in ten
people are affected by gluten, the health impact is enormous. Understanding the gluten syndrome is
important for the health of the global community.”
Perlmutter starts summarizing the chapter by telling us that
he has inundated us with all of this data because even though we may not be as sensitive
to gluten as an individual with celiac, the data shows we may all be sensitive
to gluten from a neurological stand-point.
In this chapter, Perlmutter wants us to get a scope of the problem, as
he sees it, and wants us to have a firm understanding that gluten can be the
root cause behind inflammation in our system that can have a damaging impact on
more than just our gut. He is absolutely
convinced that this inflammation damages our brain, too, and he does his best
in chapter 2 to introduce us to enough data that we begin to consider the
possibility that he may be right.
How does he test for gluten sensitivity?
ReplyDeleteHe recommends the following tests with the ranges I've listed as desirable:
Deletefasting blood glucose: < 95 mg/deciliter (dL)
fasting insulin: < 8 uIU/dL (ideally below 3)
hemoglobin A1C: 4.8 - 5.4%
fructosamine: 188 to 223 umol/L
homocysteine: 8umol/L or less
vitamin D: 80ng/mL
C-reactive protein: 0.00 to 3.0 mg/L
gluten sensitivity test with Cyrex array 3 test (He highly recommends the Cyres array 3 test from Cyrex labs. He saus that it is the best test on the market for gluten sensitivity. This link is on his website drperlmutter.com http://www.cyrexlabs.com/CyrexTestsArrays/tabid/136/Default.aspx