Content uploaded by Csaba Tóth
Author content
All content in this area was uploaded by Csaba Tóth on Aug 22, 2016
Content may be subject to copyright.
CASE REPORT PEER REVIEWED | OPEN ACCESS
www.edoriumjournals.com
International Journal of Case Reports and Images (IJCRI)
International Journal of Case Reports and Images (IJCRI) is
an international, peer reviewed, monthly, open access, online
journal, publishing high-quality, articles in all areas of basic
medical sciences and clinical specialties.
Aim of IJCRI is to encourage the publication of new information
by providing a platform for reporting of unique, unusual and
rare cases which enhance understanding of disease process,
its diagnosis, management and clinico-pathologic correlations.
IJCRI publishes Review Articles, Case Series, Case Reports,
Case in Images, Clinical Images and Letters to Editor.
Website: www.ijcasereportsandimages.com
Crohn’s disease successfully treated with the paleolithic
ketogenic diet
Csaba Tóth, Andrea Dabóczi, Mark Howard, Nicholas J. Miller,
Zsóa Clemens
ABSTRACT
Introduction: Crohn’s disease is regarded as having no curative treatment. Previous
reports on dietary therapy of Crohn’s disease indicate no major success.
Case Report: Here we report a severe case of Crohn’s disease where we successfully
applied the paleolithic ketogenic diet. Dietary therapy resulted in resolution of symptoms,
normalized laboratory parameters as well as gradual normalization of bowel inammation
as evidenced by imaging data and normalization of intestinal permeability as shown by the
polyethylene glycol (PEG 400) challenge test. The patient was able to discontinue medication
within two weeks. Currently, he is on the diet for 15 months and is free of symptoms as well
as side effects.
Conclusion: We conclude that the paleolithic ketogenic diet was feasible, effective and safe
in the present case.
(This page in not part of the published article.)
International Journal of Case Reports and Images, Vol. 7 No. 9, September 2016. ISSN – [0976-3198]
Int J Case Rep Images 2016;7(9):570–578.
www.ijcasereportsandimages.com
Tóth et al. 570
CASE REPORT OPEN ACCESS
Crohn’s disease successfully treated with the paleolithic
ketogenic diet
Csaba Tóth, Andrea Dabóczi, Mark Howard, Nicholas J. Miller,
Zsófia Clemens
ABSTRACT
Introduction: Crohn’s disease is regarded as
having no curative treatment. Previous reports
on dietary therapy of Crohn’s disease indicate
no major success. Case Report: Here we report
a severe case of Crohn’s disease where we
successfully applied the paleolithic ketogenic
diet. Dietary therapy resulted in resolution of
symptoms, normalized laboratory parameters
as well as gradual normalization of bowel
inflammation as evidenced by imaging data
and normalization of intestinal permeability
as shown by the polyethylene glycol (PEG 400)
challenge test. The patient was able to discontinue
medication within two weeks. Currently, he is on
the diet for 15 months and is free of symptoms
as well as side effects. Conclusion: We conclude
that the paleolithic ketogenic diet was feasible,
effective and safe in the present case.
Keywords: Crohn’s disease, Dietary therapy, In-
flammatory bowel disease, Ketogenic diet, Paleo-
lithic diet
Csaba Tóth1, Andrea Dabóczi1, Mark Howard2, Nicholas J.
Miller2, Zsófia Clemens1,3
Affiliations: 1Paleomedicina Hungary Ltd., Evolutionary
Medicine Working Group, Budapest, Hungary; 2Biolab Medical
Unit, London, United Kingdom; 3Neurological Department,
University of Pécs, Pécs, Hungary.
Corresponding Author: Zsófia Clemens, PhD, Paleomedicina
Hungary Ltd., Evolutionary Medicine Working Group, Hidász
u. 3. H-1026, Budapest, Hungary; Department of Neurology,
University of Pécs, Rét u. 2, H-7623, Pécs, Hungary; Email:
clemenszsofia@gmail.com
Received: 17 April 2016
Accepted: 03 June 2016
Published: 01 September 2016
How to cite this article
Tóth C, Dabóczi A, Howard M, Miller NJ, Clemens
Z. Crohn’s disease successfully treated with the
paleolithic ketogenic diet. Int J Case Rep Images
2016;7(10):570–578.
Article ID: Z01201609CR10690CT
*********
doi:10.5348/ijcri-2016102-CR-10690
INTRODUCTION
Crohn’s disease, an inflammatory disease of the
bowel, is regarded as having no cure [1]. Standard
treatment which involves steroids, immunosuppressants
and biological therapy is aimed at reducing symptoms
[1]. Periods of flares and remissions typically alternate,
however, the overall course of the disease is progressive.
A set of ecological evidence, including a discrepancy
between westernized and non-westernized countries
in the occurrence of the disease, raises the possibility
of lifestyle and/or dietary factors in the etiology of the
disease [2]. There have been several attempts to use a
dietary intervention in Crohn’s disease such as the specific
carbohydrate diet [3] and the anti-inflammatory diet [4]
as well as elimination-reintroduction diets [5]. Although
clinical improvements and reduction of medicines have
been reported being associated with these diets we are
not aware of any diet inducing complete remission and
long-term freedom of medicines at the same time.
The authors of the present report are using a diet
referred to as the paleolithic ketogenic diet in the
treatment of chronic conditions. So far we have published
CASE REPORT PEER REVIEWED | OPEN ACCESS
International Journal of Case Reports and Images, Vol. 7 No. 9, September 2016. ISSN – [0976-3198]
Int J Case Rep Images 2016;7(9):570–578.
www.ijcasereportsandimages.com
Tóth et al. 571
cases of successful treatment of diabetes type 1 [6, 7] and
type 2 [8], epilepsy [9, 10] as well as other conditions [11].
CASE REPORT
Diagnosis
The 14-year-old boy presented with fatigue, low grade
fever, iron deficiency anemia, lower abdominal tenderness
and perianal dermatitis. He was of short stature for his
age. On 30 September 2013 upper and lower endoscopy
was performed. The latter showed ulcerative lesion in
the terminal ileum. Biopsy was taken from multiple sites
and histopathology showed severe inflammation of the
terminal ileum and the Bauhin’s valve. Signs of mild-
to-moderate degree aspecific inflammation were seen in
the colon. On laboratory workup inflammatory marker C
reactive protein (CRP) was elevated (58 mg/L). He was
diagnosed with Crohn’s disease.
Standard treatment
At the time of diagnosis onset (on 07 October 2013)
the patient was started on mesalazine, metronidazole
and pantoprazole. Within ten days, ciprofloxacin and
probiotics were added. Given that no improvement
was seen immunosuppressant therapy was initiated
on 13 November 2013 with azathioprine together with
methylprednisolone, potassium citrate, calcium and
vitamin D. Given that disease progressed, a year after
diagnosis onset (on 25 September 2014), biological
therapy was initiated: five cycles of adalimumab were
given each two weeks apart. The condition of the patient
further deteriorated and therefore on 07 November 2014
exclusive formula feeding was initiated. At this time
mesalazine, multivitamin, vitamin D3 and calcium were
discontinued. Pantoprazole was discontinued within two
weeks. Formula-based nutrition resulted in the resolution
of abdominal pain but other symptoms persisted (Table 1,
Figures 1 and 2).
Laboratory data
As the disease progressed iron deficiency anemia of
the patient worsened. Thrombocyte number showed a
decreasing tendency across the course of the standard
treatment. Level of inflammatory markers CRP and
erythrocyte sedimentation rate (ESR) dropped when
initiating the immunosuppressant therapy and steroid
but increased thereafter (Table 1, Figure 2).
Imaging
At the time of the diagnosis ultrasound examination
performed on 07 October 2013 showed thickening of
the terminal ileum and that of the small intestine at
multiple sites. No thickening of the colon was seen. Three
further follow-up ultrasound examinations were carried
out during the next year. This showed progression of
the disease as reflected by increasing diameter of the
thickened bowel wall and an increasing intensity of
hypervascularization. The last ultrasound out of the four
(on 7 November 2014) already indicated the thickening of
nearly all bowel segments including the colon ascendens
and the colon transversum. Figure 3 shows as the largest
diameter of the terminal ileum changed between 7
October 2013 and 7 November 2014.
Magnetic Resonance Enterography
Magnetic resonance enterography performed five
weeks after diagnosis onset (on 12 November 2013)
indicated thickening of the small intestinal wall at
multiple locations. A follow-up magnetic resonance
enterography 13 months later, on 16 December 2014,
showed an increase in the variability in the diameter of
the bowel lumen and narrowing of the lumen (Figure 4).
Due to the narrowing the patient was offered surgery in
December 2014 which he refused.
Symptoms
Abdominal cramps as well as episodes of low grade
fever lessened when initiating the immunosuppressant
therapy together with steroid. However, within three
months the patient developed bilateral knee pain as a
new symptom. Later on his appetite deteriorated. At
12 months after diagnosis onset abdominal cramps
increased and episodes of low grade fever returned. The
patient reported fatigue along with a deterioration in his
school performance. Following the onset of the biological
therapy all symptoms persisted. Following the fourth cycle
of adalimumab strong abdominal pain emerged abruptly
which persisted for several hours. Given this experience
and the overall ineffectiveness of the biological therapy
the patient decided to stop it. He was put on exclusive
enteral nutrition which resulted in a lessening of his
abdominal cramps but other symptoms persisted.
Dietary advices while on the standard
therapy
The patient was advised to follow a diet free of lactose
and low in fat and fibers. Analysis of his diet-symptom
diary did not show any consistent association between
symptoms and food items.
Intervention with the paleolithic
ketogenic diet
Given the ineffectiveness of standard therapies the
parents of the child were seeking for alternative options.
When we first met the patient he reported bilateral pain
and swelling of the knee, frequent episodes of fever
and night sweats as well as fatigue. He looked pale. We
offered the paleolithic ketogenic diet along with close
monitoring of the patient. The patient started the diet
on 4 January 2015. The diet is consisting of animal fat,
meat, offal and eggs with an approximate 2:1 fat : protein
International Journal of Case Reports and Images, Vol. 7 No. 9, September 2016. ISSN – [0976-3198]
Int J Case Rep Images 2016;7(9):570–578.
www.ijcasereportsandimages.com
Tóth et al. 572
ratio. Red and fat meats instead of poultry as well as
regular intake of organ meats from pork and cattle were
encouraged. Grains, milk, dairy, refined sugars, vegetable
oils, oilseeds, nightshades and artificial sweeteners
were excluded. Small amount of honey was allowed for
sweetening. The patient was not taking any supplements.
Regular home monitoring of urinary ketones indicated
sustained ketosis. Regular laboratory follow-up was used
to monitor the course of the disease as well as for giving
feedback how to fine tune the diet. The patient was under
our close control and gave frequent feedbacks and so we
could assess the level of dietary compliance. The patient
maintained a high level dietary adherence on the long-
term, yet on his birthday, he made a mistake: he has
eaten two pieces of commercially available “paleo” cake
which contained coconut oil, flour from oilseeds as well
as sugar alcohol. Clinical consequences are discussed
later. From July 2015 onwards he also consumed small
amounts of vegetables and fruits. Given the persistence of
certain alterations in laboratory values (mild anemia) on
10 November 2015, despite 10 months on the paleolithic
ketogenic diet, we suggested to tighten the diet again.
From this time on he did neither consume vegetables and
fruits nor vegetable oil containing spices such as cumin
and cinnamon.
We obtained written informed consent from the
patient for the publication of his case.
RESULTS
Discontinuing medication
Within two weeks after diet onset the patient
discontinued azathioprine, the only medicine he was
taking at this time. Currently, he is without medicines for
15 months.
Symptoms
The frequent night sweats of the patient disappeared
within three weeks after diet onset and thus his sleep
improved significantly. The knee pains of the patient
began to lessen at 4th week on the diet and completely
disappeared by the third month. From this time onwords
he regularly went to school by bike (20 km daily). He
reported restored energy and increased physical and
mental fitness. Although during the eight months before
diet onset his weight was declining, following diet onset he
began to gain weight. At diet onset his weight was 41 kg and
was 152 cm tall (BMI = 17.7). At 12 months after diet onset,
his height was 160 cm and weighted 50 kg (BMI: 19.5).
The change in his height and weight is depicted in Figure
5. At the time of writing the article he is on the diet for 15
months and is free of symptoms as well as side effects.
Laboratory workup
Laboratory workup including blood and urinary
analysis was performed seven times during follow-up.
Urinary ketones were positive on each occasion. Blood
glucose was between 5 and 5.4 mmol/l. Renal and liver
function as well as ions were normal. His severe iron
deficiency anemia was reversed already on the fourth
week of the diet: iron level increased from 3.6 μmol/L
to 12.1 μmol/L. Inflammatory markers including ESR
and CRP decreased significantly: at four weeks CRP
was 3.75 mg/L while ESR was 3 mm/h (Figure 2).
Thereafter inflammatory markers elevated to some
extent. Thrombocyte number was already low before diet
onset but decreased further following diet onset. The last
laboratory follow-up, however, on 14 December 2015,
indicated an increase in thrombocyte number (Table 2.).
Imaging
Ultrasound examination of the abdomen was carried
out five times during follow-up and was performed
by the same investigator. The first examination
following the onset of the paleolithic ketogenic diet,
on 29 January 2015, showed significant improvement.
Although wall of the terminal ileum was still thickened
hypervascularization was no longer present. Thickening
was still seen in the coecum and the ileum but not in the
other regions which were described as being affected
on the preceding ultrasound examination. A follow-up
exam on 09 April 2015 showed further improvement:
thickening of the wall of the terminal ileum decreased
and no abnormal was seen in any other regions. A next
ultrasound which was made following eating the “paleo
cakes” showed thickening of the wall of the terminal
ileum to as much as 6 mm. On the next examination, on
19 Jun 2015, thickening of the terminal ileum decreased
to 4.5 cm. Three months later, on 17 September 2015, the
examination showed no abnormality (Figures 2 and 3).
Intestinal permeability test
Intestinal permeability was assessed using a
polyethylene glycol (PEG 400) challenge test based on
the method of Chadwick et al. [12]. PEG 400 contains a
mixture of inert water soluble molecules of 11 different
sizes that are absorbed independently of dose, but which
display decreasing mucosal transport with increasing
molecular size. PEG 400 is also nontoxic, not degraded
by intestinal bacteria, not metabolized by tissues, and
rapidly excreted in urine. After a 3.0-gram oral dose of
PEG, the subject makes a six-hour urine collection. The
PEG fractions are acetylated with acetic anhydride, using
pyridine as a catalyst, and then quantitated by capillary
gas-liquid chromatography. The percentage of each
fraction of PEG excreted over 6 hours is calculated.
PEG 400 challenge test performed at four months on
the diet (on 18 May 2015) showed increased permeability
to PEG between 242 and 418 molecular weight. A
follow-up test performed at 10 months on the diet (on
26 November 2015) showed no abnormal intestinal
permeability (Figure 6).
International Journal of Case Reports and Images, Vol. 7 No. 9, September 2016. ISSN – [0976-3198]
Int J Case Rep Images 2016;7(9):570–578.
www.ijcasereportsandimages.com
Tóth et al. 573
Table 1: Laboratory data while on a standard diet and corresponding medications, Dashes indicate that a given parameter was not
measured
04 Oct
2013
17 Oct
2013
25 Nov
2013
17 Dec
2013
27 Mar
2014
04 Sep
2014
10 Nov
2014
normal
value
WBC 9.6 7.5 23.2 13.8 6.3 7.6 7.7 4.5-11.5 G/L
RBC 5.5 5.3 5.6 5.5 4.2 4.4 4.7 4.5-5.9 T/L
Hgb 117 113 130 133 110 119 132 135-170 g/L
Hct 0.38 0.36 0.41 0.41 0.33 0.35 0.39 0.41-0.51 L/L
Thrombocyte 252 285 311 168 128 240 166 150-400 G/L
CRP 23.1 21.1 2.6 2.4 12.3 46.7 19.6 0-5 mg/L
ESR 12 8 1 1 14 25 15 0-15 mm/h
T. protein 59 53.9 57.9 54.4 58.3 61.6 57.3 57-80 g/L
Carbamide 0.8 1.7 4.2 5 3.5 2.7 2.8 2.8-7.2 mmol/L
Creatinine 49 47 44 58 41 45 56 53-100 μmol/L
Sodium 140 142 140 136 - - 143 135-145 mmol/L
Potassium citrate 4.5 4.1 3.9 4.1 - - 4.5 3.2-5.1 mmol/L
GOT 11 18 11 10 17 15 15 0-50 U/L
GPT 6 11 12 8 7 7 7 0-50 U/L
GGT 13 23 23 15 11 15 9 0-55 U/L
Iron - - - - 6.9 3.6 - 12.5-32 μmol/L
formula feeding x
adalimumab x
multivitamin x x
calcium x x x x
vitamin D3 x x x x
potassium citrate x x
methylprednisolone x x
azathioprine x x x x x
probiotics x x
ciprofloxacin x
pantoprazole x x x x x x
metronidazole x
mesalazine x x x x x
Abbreviations: WBC: white blood cell count, RBC: red blood cell count, Hgb: hemoglobin, Hct: hematocrit, CRP: C-reactive protein,
ESR: erythrocyte sedimentation rate, T. protein: total protein, GOT: glutamate-oxaloacetate transaminase, GPT: glutamate-pyruvate
transaminase, GGT: gamma-glutamyl transferase
International Journal of Case Reports and Images, Vol. 7 No. 9, September 2016. ISSN – [0976-3198]
Int J Case Rep Images 2016;7(9):570–578.
www.ijcasereportsandimages.com
Tóth et al. 574
Figure 1: Timeline encompassing the medication of the patient,
timing and the result of the MR enterography as well as that of
the ultrasound examination.
Abbreviations: ti: thickness of the terminal ileum, *: moderate
hypervascularization, **: strong hypervascularization, IPT:
intestinal permeability test
Figure 2: Timeline encompassing medication and the change
in the inflammatory markers ESR (erythrocyte sedimentation
rate) and CRP (C reactive protein).
Figure 3: Thickness of the terminal ileum (largest diameter is
indicated) seen on ultrasound. Onset of the paleolithic ketogenic
diet as well as the occurrence of a dietary failure is indicated with
arrows. Note the improvement during the paleolithic ketogenic
diet, the relapse following the single episode of dietary failure
and the normal results on the last examination.
* indicate mild degree hypervascularization while ** high degree
hypervascularization.
Figure 4: Magnetic resonance enterography on 16 December
2014 showed thickening of the terminal ileum (arrows).
Figure 5: Weight and height of the patient during the 14 months
on the standard treatment and following the onset of the dietary
therapy.
Figure 6: PEG 400 challenge test showing increased intestinal
permeability to PEG from molecular weight 242 to molecular
weight 418 at four months on the diet (A) while no abnormal at
10 months (B).
DISCUSSION
Here we report a case where Crohn’s disease was
reversed by the paleolithic ketogenic diet.
Disease symptoms began to improve a few weeks
after diet onset. Within 10 months the patient achieved
full remission from symptoms as well as normalization
of intestinal inflammation as evidenced by imaging data,
normalization of laboratory parameters and that of the
International Journal of Case Reports and Images, Vol. 7 No. 9, September 2016. ISSN – [0976-3198]
Int J Case Rep Images 2016;7(9):570–578.
www.ijcasereportsandimages.com
Tóth et al. 575
intestinal permeability. Aside from a single dietary fault
the patient strictly adhered to the diet as assessed by
frequent patient feedback, laboratory data and home
monitoring of urinary ketones. Given the patient’s severe
condition upon the first visit the paleolithic ketogenic
diet was started in the strictest form thus containing no
vegetables and fruits at all. Such a diet may first sound
restrictive but our previous experience indicate that a
full fat-meat diet is needed in the most severe cases of
Crohn’s disease. In addition, our experience shows that
even a single occasion of deviation from diet rules may
result in lasting relapse. This was the case in the present
patient too where breaking the strict rules (eating the
”paleo cakes”) resulted in a thickening of the bowel wall.
Based on our experience this is due to the components
of the popular paleolithic diet including coconut oil, oil
seeds and sugar alcohols which may trigger inflammation.
In contrast, honey, consumed in limited amounts is
tolerable and does not cause such symptoms. The
significant improvement seen in the last laboratory exam
also indicates that the paleolithic ketogenic diet is most
effective when containing no plant components at all.
Crohn’s disease is known to be characterized by a
progressive worsening of symptoms. Standard therapies
may result in a temporary symptom relief but are
accompanied by significant side effects [1]. Surgical
resection is thought to be inevitable on the long-term [13].
Our patient also failed to respond to immunosuppressive
therapies, steroid, biological agents and exclusive formula
feeding. Within 14 months after diagnosis onset, he was
offered surgery due to the narrowing of the bowel. The
paleolithic ketogenic diet reversed the disease from this
Table 2: Laboratory data while on the paleolithic ketogenic diet with no medications. Dashes indicate that a given parameter was not
measured
02 Feb
2015
09 Apr
2015
29 Apr
2015
19 Jun
2015
17 Sep
2015
10 Nov
2015
14 Dec
2015
normal value
WBC 7.1 8.5 5.7 7.1 7.1 7.8 8 4.5–11.5 G/L
RBC 5 4.8 4.8 5.2 4.8 5.3 5.4 4.5–5.9 T/L
Hgb 145 135 137 147 135 146 151 135–170 g/L
Hct 0.42 0.39 0.4 0.42 0.39 0.43 0.44 0.41–0.51 L/L
Thrombocyte 71 75 68 82 95 65 100 150–400 G/L
CRP 3.75 9.9 9.3 1.8 14.3 4.4 7.1 0–5 mg/L
ESR 3 8 8 5 10 6 5 0–15 mm/h
Total protein 60 62 - - 63 65 66 57–80 g/L
Carbamid 5.3 6.2 - - 5.8 6.3 6.9 2.8–7.2 mmol/L
Creatinine 53 63 - - 48 66 7.3 53–100 μmol/L
Sodium 141 138 - - 139 140 139 135–145 mmol/L
Potassium 4.3 3.9 - - 4.1 4.1 4.2 3.2–5.1 mmol/L
GOT 18 20 - - 21 24 24 0–50 U/L
GPT 12 14 - - 18 18 18 0–50 U/L
GGT 12 13 - - 13 13 12 0–55 U/L
Iron 12.1 10.3 - - 10.6 11 13.7 12.5–32 μmol/L
Uric acid 258 264 - - 332 329 329 208–428 μmol/L
Glucose 5 5 - - 5.3 5.2 5.4 3.5–6.1 mmol/L
Magnesium 0.76 0.86 - - 0.81 0.87 0.89 0.73–1.06 mmol/L
Cholesterol 4.6 4.9 4.7 4.8 4.3 4.1 4.3 <5.2 mmol/L
Trigliceride 0.9 1.46 - - 0.56 0.93 1.34 <1.7 mmol/L
Fibrinogen - - 2.5 2.3 - - - 2-4 g/L
Urinary ketones ++ ++++ ++ +++ +++ ++ +
Abbreviations: WBC: white blood cell count, RBC: red blood cell count, Hgb: hemoglobin, Hct: hematocrit, CRP: C-reactive protein,
ESR: erythrocyte sedimentation rate, T. protein: total protein, GOT: glutamate-oxaloacetate transaminase, GPT: glutamate-pyruvate
transaminase, GGT: gamma-glutamyl transferase.
International Journal of Case Reports and Images, Vol. 7 No. 9, September 2016. ISSN – [0976-3198]
Int J Case Rep Images 2016;7(9):570–578.
www.ijcasereportsandimages.com
Tóth et al. 576
very advanced stage. Although Crohn’s disease is known
to be characterized by an alternation of better and worse
periods, a complete remission from a very advanced stage
is highly unlikely to be the part of the normal course of
the disease.
While on the biological therapy thrombocyte number
dropped and continued to decrease while on the diet. Our
previous experience does not indicate thrombocytopenia
on the paleolithic ketogenic diet. However, low
thrombocyte number is a well-known side effect of
the use of adalimumab in Crohn’s disease [14, 15]. It
is also noteworthy that a return to the strictest form of
the paleolithic ketogenic diet resulted in an increase in
thrombocyte number.
Crohn’s disease is regarded as an autoimmune disease.
Autoimmune diseases and Crohn’s disease specifically
have been linked to increased intestinal permeability
[16]. Yet currently there is no known means to reverse
pathological intestinal permeability [17]. A previous study
with the paleolithic diet found no change in intestinal
permeability as assessed by the lactulose-mannitol test
[18]. As far as we know this is the first documented case
where pathological intestinal permeability was reversed
as assessed by a diagnostic test.
Experts in the field of evolutionary medicine has
long been suggesting that chronic diseases of civilization
emerge from a mismatch between our ancient genome and
current lifestyles [19, 20]. In recent years an increasing
number of studies showed that the metabolic syndrome
and associated conditions can be reversed or improved by
applying a diet denoted as ”paleolithic” (for a review see:
[21]). In the paleolithic diet, as described in the implied
papers, macronutrient ratios are undefined or variable,
as well as that of the ratio of animal/plant foods including
the ratio of animal/plant fats. Our clinical experience,
however, indicate that the most severe chronic conditions,
including the Crohn’s disease, can only be reversed by
the paleolithic ketogenic diet based on animal fat, meat
and offal. A same conclusion was drawn in our previous
case study showing that the paleolithic ketogenic diet was
more effective than the popular form of the paleolithic
diet in the case of Gilbert’s syndrome [11]. The paleolithic
ketogenic diet we use in the treatment of chronic diseases
is close to the evolutionary diet originally proposed by
gastroenterologist Voegtlin [22]. With regard to the main
principals, background, sustainability and further issues
such as vitamin supply while on a meat-fat based diet we
refer to the excellent book of Voegtlin [22].
As regards the underlying mechanism, we put forward
that normalizing pathological intestinal permeability
is crucial in tackling autoimmune diseases, including
Crohn’s disease. Accordingly, increased intestinal
permeability has been shown to predict relapses in
Crohn’s disease [23]. It is known that under physiological
conditions, dietary macromolecules are not transported
paracellularly from the intestinal lumen to the blood or
the lymph. It has been suggested that certain components
of the Western-type diet are able to destroy cell junctions
and thereby compromise the intestinal barrier function
[24, 25]. As a result, large molecules including protein
fragments and glycoproteins, possessing antigenic
properties, may appear in the circulation and promote
chronic inflammation [26]. Given their specific structure,
these macromolecules may bind to and form complexes
with the surface molecules of certain cell types. Such
a complex is then destroyed by the immune system
through apoptosis [27, 28]. We assume that a continued
exposition to these macromolecules may maintain the
autoimmune destruction of tissues. We put forward that
the animal fat-meat based diet, the only diet humans
are evolutionary adapted to, is lacking substances that
are destroying the intestinal barrier. A shift toward
the paleolithic ketogenic diet may normalize intestinal
permeability (as also seen in our patient) and thereby
may halt the autoimmune destruction of the affected
tissues, in our case the intestine. With the attenuation of
the autoimmune process the intestine may regenerate.
CONCLUSION
We conclude that the paleolithic ketogenic diet was
effective while producing no side effects in this case of
Crohn’s disease. In contrast to standard therapeutic
approaches which are aimed to control certain
components of the disease only, the paleolithic ketogenic
diet was able to reverse the cluster of symptoms and
abnormalities associated with the disease. Assuming a
long term dietary compliance, we believe that the patient
would remain disease-free in the future.
*********
Author Contributions
Csaba Tóth – Substantial contributions to conception and
design, Acquisition of data, Analysis and interpretation
of data, Drafting the article, Revising it critically for
important intellectual content, Final approval of the
version to be published
Andrea Dabóczi – Acquisition of data, Analysis and
interpretation of data, Revising it critically for important
intellectual content, Final approval of the version to be
published
Mark Howard – Acquisition of data, Analysis and
interpretation of data, Revising it critically for important
intellectual content, Final approval of the version to be
published
Nicholas J. Miller – Acquisition of data, Analysis and
interpretation of data, Drafting the article, Revising
it critically for important intellectual content, Final
approval of the version to be published
Zsófia Clemens – Substantial contributions to
conception and design, Acquisition of data, Analysis
and interpretation of data, Drafting the article, Revising
it critically for important intellectual content, Final
approval of the version to be published
International Journal of Case Reports and Images, Vol. 7 No. 9, September 2016. ISSN – [0976-3198]
Int J Case Rep Images 2016;7(9):570–578.
www.ijcasereportsandimages.com
Tóth et al. 577
Guarantor
The corresponding author is the guarantor of submission.
Conflict of Interest
Authors declare no conflict of interest.
Copyright
© 2016 Csaba Tóth et al. This article is distributed under
the terms of Creative Commons Attribution License which
permits unrestricted use, distribution and reproduction in
any medium provided the original author(s) and original
publisher are properly credited. Please see the copyright
policy on the journal website for more information.
REFERENCES
1. Akobeng AK. Crohn’s disease: current treatment
options. Arch Dis Child 2008 Sep;93(9):787–92.
2. Barreiro-de Acosta M, Alvarez Castro A, Souto
R, Iglesias M, Lorenzo A, Dominguez-Muñoz JE.
Emigration to western industrialized countries: A risk
factor for developing inflammatory bowel disease. J
Crohns Colitis 2011 Dec;5(6):566–9.
3. Cohen SA, Gold BD, Oliva S, et al. Clinical and
mucosal improvement with specific carbohydrate diet
in pediatric Crohn disease. J Pediatr Gastroenterol
Nutr 2014 Oct;59(4):516–21.
4. Olendzki BC, Silverstein TD, Persuitte GM, Ma Y,
Baldwin KR, Cave D. An anti-inflammatory diet as
treatment for inflammatory bowel disease: a case
series report. Nutr J 2014 Jan 16;13:5.
5. Donnellan CF, Yann LH, Lal S. Nutritional
management of Crohn’s disease. Therap Adv
Gastroenterol 2013 May;6(3):231–42.
6. Tóth C, Clemens Z. Type 1 diabetes mellitus
successfully managed with the paleolithic ketogenic
diet. Int J Case Rep Images 2014;5:699–703.
7. Tóth C, Clemens Z. A child with type 1 diabetes mellitus
(T1DM) successfully treated with the Paleolithic
ketogenic diet: A 19-month insulin freedom. Int J
Case Rep Images 2015;6:752–7.
8. Tóth C, Clemens Z. Successful treatment of a patient
with obesity, type 2 diabetes and hypertension with
the paleolithic ketogenic diet. Int J Case Rep Images
2015;6:161–7.
9. Clemens Z, Kelemen A, Fogarasi A, Tóth C. Childhood
absence epilepsy successfully treated with the
paleolithic ketogenic diet. Neurol Ther 2013 Sep
21;2(1-2):71–6.
10. Clemens Z, Kelemen A, Tóth C. NREM-sleep
Associated Epileptiform Discharges Disappeared
Following a Shift toward the Paleolithic Ketogenic
Diet in a Child with Extensive Cortical Malformation.
Am J Med Case Rep 2015;3:212–5.
11. Tóth C, Clemens Z. Gilbert’s Syndrome Successfully
Treated with the Paleolithic Ketogenic Diet. Am J
Med Case Rep 2015;3:117–20.
12. Chadwick VS, Phillips SF, Hofmann AF.
Measurements of intestinal permeability using low
molecular weight polyethylene glycols (PEG 400). I.
Chemical analysis and biological properties of PEG
400. Gastroenterology 1977 Aug;73(2):241–6.
13. Baumgart DC, Sandborn WJ. Crohn’s disease. Lancet
2012 Nov 3;380(9853):1590–605.
14. Salar A, Bessa X, Muñiz E, Monfort D, Besses C,
Andreu M. Infliximab and adalimumab-induced
thrombocytopenia in a woman with colonic Crohn’s
disease. Gut 2007 Aug;56(8):1169–70.
15. Casanova MJ, Chaparro M, Martínez S, Vicuña
I, Gisbert JP. Severe adalimumab-induced
thrombocytopenia in a patient with Crohn’s disease.
J Crohns Colitis 2012 Dec;6(10):1034–7.
16. Hollander D. Crohn’s disease--a permeability disorder
of the tight junction? Gut 1988 Dec;29(12):1621–4.
17. Odenwald MA, Turner JR. Intestinal permeability
defects: is it time to treat? Clin Gastroenterol Hepatol
2013 Sep;11(9):1075–83.
18. Boers I, Muskiet FA, Berkelaar E, et al. Favourable
effects of consuming a Palaeolithic-type diet on
characteristics of the metabolic syndrome: a
randomized controlled pilot-study. Lipids Health Dis
2014 Oct 11;13:160.
19. Cordain L. The Paleo Diet: Lose Weight and Get
Healthy by Eating the Foods You Were Designed to
Eat. New York: John Wiley; 2002.
20. Lindeberg S. Food and western disease: health
and nutrition from an evolutionary perspective.
Chichester: Wiley-Blackwell; 2009.
21. Manheimer EW, van Zuuren EJ, Fedorowicz Z, Pijl
H. Paleolithic nutrition for metabolic syndrome:
systematic review and meta-analysis. Am J Clin Nutr
2015 Oct;102(4):922–32.
22. Voegtlin WL. The stone age diet: based on in-depth
studies of human ecology and the diet of man. New
York: Vantage Press; 1975.
23. Wyatt J, Vogelsang H, Hübl W, Waldhöer T, Lochs H.
Intestinal permeability and the prediction of relapse in
Crohn’s disease. Lancet 1993 Jun 5;341(8858):1437–
9.
24. de Punder K, Pruimboom L. The dietary intake
of wheat and other cereal grains and their role in
inflammation. Nutrients 2013 Mar 12;5(3):771–87.
25. Lerner A, Matthias T. Changes in intestinal tight
junction permeability associated with industrial food
additives explain the rising incidence of autoimmune
disease. Autoimmun Rev 2015 Jun;14(6):479–89.
26. Ménard S, Cerf-Bensussan N, Heyman M. Multiple
facets of intestinal permeability and epithelial
handling of dietary antigens. Mucosal Immunol 2010
May;3(3):247–59.
27. Cordain L, Toohey L, Smith MJ, Hickey MS.
Modulation of immune function by dietary lectins in
rheumatoid arthritis. Br J Nutr 2000 Mar;83(3):207–
17.
28. Maverakis E, Kim K, Shimoda M, et al. Glycans in the
immune system and The Altered Glycan Theory of
Autoimmunity: a critical review. J Autoimmun 2015
Feb;57:1–13.
International Journal of Case Reports and Images, Vol. 7 No. 9, September 2016. ISSN – [0976-3198]
Int J Case Rep Images 2016;7(9):570–578.
www.ijcasereportsandimages.com
Tóth et al. 578
Access full text article on
other devices
Access PDF of article on
other devices
EDORIUM JOURNALS AN INTRODUCTION
Edorium Journals: On Web
About Edorium Journals
Edorium Journals is a publisher of high-quality, open ac-
cess, international scholarly journals covering subjects in
basic sciences and clinical specialties and subspecialties.
Edorium Journals
www.edoriumjournals.com
Edorium Journals et al.
Edorium Journals: An introduction
Edorium Journals Team
But why should you publish with Edorium
Journals?
In less than 10 words - we give you what no one does.
Vision of being the best
We have the vision of making our journals the best and
the most authoritative journals in their respective special-
ties. We are working towards this goal every day of every
week of every month of every year.
Exceptional services
We care for you, your work and your time. Our efficient,
personalized and courteous services are a testimony to this.
Editorial Review
All manuscripts submitted to Edorium Journals undergo
pre-processing review, first editorial review, peer review,
second editorial review and finally third editorial review.
Peer Review
All manuscripts submitted to Edorium Journals undergo
anonymous, double-blind, external peer review.
Early View version
Early View version of your manuscript will be published
in the journal within 72 hours of final acceptance.
Manuscript status
From submission to publication of your article you will
get regular updates (minimum six times) about status of
your manuscripts directly in your email.
Our Commitment
Favored Author program
One email is all it takes to become our favored author.
You will not only get fee waivers but also get information
and insights about scholarly publishing.
Institutional Membership program
Join our Institutional Memberships program and help
scholars from your institute make their research accessi-
ble to all and save thousands of dollars in fees make their
research accessible to all.
Our presence
We have some of the best designed publication formats.
Our websites are very user friendly and enable you to do
your work very easily with no hassle.
Something more...
We request you to have a look at our website to know
more about us and our services.
We welcome you to interact with us, share with us, join us and of course publish with us.
Browse Journals
CONNECT WITH US
Invitation for article submission
We sincerely invite you to submit your valuable
research for publication to Edorium Journals.
Six weeks
You will get first decision on your manuscript within six
weeks (42 days) of submission. If we fail to honor this
by even one day, we will publish your manuscript free
of charge.*
Four weeks
After we receive page proofs, your manuscript will be
published in the journal within four weeks (31 days).
If we fail to honor this by even one day, we will pub-
lish your manuscript free of charge and refund you
the full article publication charges you paid for your
manuscript.*
This page is not a part of the published article. This page is an introduction to Edorium Journals and the publication services.
* Terms and condition apply. Please see Edorium Journals website for
more information.