Effect Vitamin K2-7 Peripheral Neuropathy
Effect Vitamin K2-7 Peripheral Neuropathy
Effect Vitamin K2-7 Peripheral Neuropathy
ABSTRACT
Objective: To evaluate the activity and tolerability of Vitamin K2-7 (MK-7) in a series of patients with peripheral neuropathy due to
vitamin B12 deficiency and / or diabetes mellitus.
Material and Methods: An open labeled clinical study was conducted in 30 patients presenting with peripheral neuropathy and
suffering from either megaloblastic anaemia (viamin B12 deficient) and/ or diabetes mellitus. Vitamin B12 levels in blood were estimated at
baseline and during therapy. Vitamin K2-7 capsules (100 mcg / capsule, twice a day) was given orally for 8 weeks. Patients kept a regular
record of the intensity of the symptoms during the baseline and throughout the study. Symptoms included tingling and numbness along
with weakness, fatigue and cramps. The intensity of the symptoms was assessed on a Visual Analog Scale (VAS). They were followed
up to 8 weeks. Blood biochemical and organ function tests were studied at the baseline, at the fourth week and at the end of the eight
week. Prior to the study Ethics Committee Approval was obtained from the Ethics Committee of T. N. M. C. & B. Y. L. Nair Ch. Hospital.
The trial was registered with Clinical Trial Registry of India (CTRI). (CTRI/2012/08/002930). Informed written consent was obtained from
the patients before enrollment.
Results: Depending on the basal VAS score the patients were divided in a moderate group and a severe group. The moderate group had
VAS score of 6-8 and the severe group had a VAS score of 8-9. By the end of eight week, the VAS score in both the groups was reduced to
1-2. The intensity specifically of tingling and numbness has reduced to a much greater extent. It was of interest to observe that ten out of 23
patients of Vitamin B12 deficiency group had residual neuropathic symptoms in-spite of adequate levels of Vitamin B12 following vitamin
B12 administration. The residual neuropathic symptom score reduced following Vitamin K2-7 therapy. Vitamin K2-7 was well tolerated
clinically and found to be safe as per the organ functions in all the patients. No adverse events were reported during the period of therapy.
Conclusion: This preliminary study has shown that vitamin K2-7 at a dose of 100 mcg twice a day for 8 weeks was well tolerated and
safe with a therapeutic activity for the symptoms of peripheral neuropathy. However, the therapeutic efficacy needs to be evaluated further
in a larger sample size, with a placebo controlled randomised double blind trial.
KEY WORDS: Vitamin K2-7, diabetes mellitus, megaloblastic anaemia, peripheral neuropathy, reverse
pharmacology.
* - Department of Haematology, B. Y. L. Nair Ch. Hospital, Dr. A. L. Nair Road, Mumbai Central, Mumbai.
**- Viridis BioPharma Pvt. Ltd., V. N. Purav Marg, Chunabhatti, Mumbai. ***- Consultant Haematologist; -
ICMR Advance Centre of Reverse Pharmacology in Traditional Medicine, Medical Research Center-Kasturba
Health Society, Mumbai. Correspondence to: Dr V K Kulkarni, 7, Shefalee, Makarand Society, Veer Savarkar
Marg, Mahim, Mumbai - 400016 Email: vitamink2beuropathy@gmail.com
P
Ch. Hospital.
eripheral neuropathy is a common problem
faced by a large number of patients. Its Subjects
aetiology is multifactorial. Most common
causes would be megaloblastic anaemia and diabe- For the study 38 patients of age 18-60 years
tes mellitus. India is considered to be the diabetic were screened. A written informed consent (ap-
capital of the world.1 The total number of people proved by the ethics committee) was taken from all
with diabetes is projected to rise from 171 million the patients. Out of 38 patients screened, 8 patients
in 2000 to 366 million in 2030.2 Megaloblastic did not report back. The remaining 30 patients
anaemia and vitamin B12 deficiency are often were enrolled in the study. Out of these 30 patients
missed and is frequently neglected. There is a high 23 patients (male 13 and female 10) were suffering
incidence in the vegetarian population. The mani- from megaloblastic anaemia and 7 patients (male
festations of neuropathy in these conditions varies 3 and female 4) had diabetes mellitus. The patients
from mild to severe with symptoms of sensory and were divided in two groups based upon the vali-
motor defects which reduces the quality of life and dated visual analog scale score for the degree of
productivity. severity of symptoms of peripheral neuropathy
(tingling and numbness along with weakness,
One added cause of iatrogenic neuropathy in fatigue and cramps). The group A (Severe) had a
diabetes mellitus is the treatment with Metformin VAS score of 8 - 9 and group B (Moderate) with a
that leads to vitamin B12 deficiency. Persistence of score of 6 - 8.
neuropathy symptoms despite routine treatment is
a well identified unmet medical need. The study procedure and assessments
Two of the authors (DSM and ABV) of the Thirty patients after a proper history, exami-
present study had earlier observed that Vit.k2-7 nation and investigations were selected as per
relieves idiopathic muscle cramps as well as symp- the criteria of choice mentioned in the protocol.
toms of diabetic neuropathy. 3 Blood investigations viz. complete blood counts
Taking a lead from this serendipitous discov- with ESR, vitamin B-12, homocysteine, glycosyl-
ery it was decided to conduct an open labeled ated haemoglobin, glucose tolerance test, fasting
reverse pharmacological study of Vitamin K2-7 and post prandial plasma glucose, PT-INR, liver
(MK-7) in 30 patients with peripheral neuropa- function tests and renal function tests were done
thy. Appropriate permission from the Ethics at the base line, at the fourth week and at the end
Committee (EC) of T. N. M. C. & B. Y. L. Nair Ch. of the study. The patients were assessed at follow
Hospital was obtained prior to the study. This ups at 1st week, 2nd week, 3rd week, 4th week, 7th
clinical study was registered with Clinical Trial week and 9th week. A detailed physical (general
Registry of India (CTRI). (CTRI/2012/08/002930) and systemic) examination was done at the base-
line and at every visit. A predesigned case record
Material and Methods form (approved by the Ethics Committee) which
included a page of adverse events was used. The
Study Design patients were given 2 capsules (100 mcg each) a
day of Vitamin K2-7 (Viridis BioPharma Pvt. Ltd.)
This study was an open labeled observational
for 8 weeks. The subjective severity of the symp-
study for evaluation of activity and tolerability
toms of peripheral neuropathy was assessed with
of vitamin K2-7 (MK-7)
validated VAS from 0 to
in patients of diabetes
The subjective severity of the symptoms of pe- 10 (nil to unbearable) be-
mellitus and megalo-
fore, at the end of fourth
blastic anaemia with ripheral neuropathy was assessed with validated
week and at the end of
peripheral neuropathy. VAS from 0 to 10 (nil to unbearable) before, at the
therapy. The safety was
Reverse pharmacologi- end of fourth week and at the end of therapy. assessed by clinical tol-
cal approach was ap-
erability, adverse events and by any change in the bottles to patients at the time of the enrollment and
organ function tests. The therapeutic activity was at an interval of every 15 days. Patient ingested a
assessed by noting the reduction in the severity of 100 mcg capsule every morning and evening after
the symptoms of peripheral neuropathy viz. tin- breakfast or snacks for 8 weeks. The drug compli-
gling and numbness along with weakness, fatigue ance was judged by counting the capsules in the
and cramps as compared to the baseline. Any other bottle brought back at the follow up visits. Patient
effect during the therapy beneficial or adverse was said to be compliant if he had consumed mini-
was also recorded. mum 80% of the total dispensed capsules.