Yay!! I don't have MS...I think?!?
just reviewing this thread. i think anyone who has spinal lesions that are "thoracic and cervical" should take any doctor's all-clear on b12 (and the b-complex in general) with a very, very large grain of salt!!!!!!!!!!
The new neuro at Mayo, in reviewing the 12 vials of blood taken for the myriad of tests she ran, combined with the MRI of brain, spine (thoracic and cervical)
i am re-submitting an item of interest from a much earlier post. from the info available at the link below, i have copied out the b12 items and highlighted points of interest.
http://www.neuro.wustl.edu/NEUROMUSCULA ... in.htm#B12
http://www.neuro.wustl.edu/NEUROMUSCULA ... in.htm#B12
CLINICAL FEATURES
Polyneuropathy
Sensory change: 2° spinal or peripheral nerve lesions
.....Early: Paresthesias
.....Loss especially of large fiber modalities
.....Distal
Motor: Later in course; Distal
Reflexes
.....Tendon: Reduced or absent at ankles
.....Plantar: Upgoing
Autonomic: Postural hypotension
CNS
Spinal cord: Earliest locus of involvement
.....Major cause of sensory & motor disability
.....Posterior column fiber loss
.....Spasticity in legs
.....Similar clinical features to N2O toxicity
Other CNS
.....Cognitive impairment in adults: Leukoencephalopathy on MRI [JL note: ie. multifocal brain white matter inflammation]
.....Mental retardation or encephalopathy in childhood syndromes
.....Sensory: Reduced smell & taste
.....Gait ataxia
Anemia: Megaloblastic; Due to reduced DNA synthesis
Gastrointestinal: Glossitis; Diarrhea
Fingernails: Hyperpigmented
TESTING
Serum
Low B12
.....Clinically significant: < 100 pg/ml
.....Suspicious: < 200 pg/ml
High homocysteine & methymalonic acid
.....Confirm biological significance of low B12 levels
MRI
Hyperintense T2 lesions in posterior columns (50%)
Lesions resolve after 8 to 12 months of therapy
Evoked potentials
.....Somatosensory: Abnormal tibial & median
.....Motor: Normal in most
PATHOLOGY
Spinal cord
Multifocal axonal loss & demyelination
Localization
.....Cervical & thoracic
.....Posterior column > Anterolateral & Anterior
Peripheral nerve: Axonal loss; Occasional ± demyelination
TREATMENT: 1 mg i.m. q 3 months
PROGNOSIS: Stabilization, or Some improvement
Paresthesias
Resolve within weeks
Rarely transient exacerbation after treatment
Myelopathy changes slowly if at all
CAUSES OF B12 DEFICIENCY: Normal body stores last 3 to 4 years
Gastrointestinal malabsorption
Deficient intrinsic factor production
.....Post-gastrectomy
.....Antibody vs parietal cells: Pernicious anemia
........Onset: Median = 60 years; Female slightly > Male
........Antibody targets: Gastric H+/K+-ATPase
...........Catalytic α subunit, and
...........Glycoprotein β subunit
........Regions of stomach affected: Fundus & body; Not antrum
........Mechanisms of B12 deficiency
...........Reduced intrinsic factor production 2° parietal cell loss
...........Antibodies to B12 binding site on intrinsic factor: Prevent formation of complex that is normally carried to terminal ileum & absorbed
.......Associated immune disorders: Thyroiditis; Diabetes; Addison's; Ovarian failure; 1° hypoparathyroidism; Graves; Vitiligo; Myasthenia gravis; Lambert-Eaton syndrome; Common variable immunodeficiency with low Ig or IgA (younger patients)
.......Associated neoplasia: Gastric carcinoma (1% to 3%)
.......Family history: 20% of relatives also have pernicious anemia; Especially 1st degree females
.......Gastritis treatment: Corticosteroids; Azathioprine
No digestion of cobalamin-R-binder complex
Pancreatic insufficiency
Consumption of cobalamin in GI tract
Intestinal bacterial overgrowth
Poor absorption by distal ileum
Sprue-related disorders
Autosomal recessive disorders
Anemia; Proteinuria; Juvenile onset
Parasitic infection: Diphyllobothrium latum
Dietary inadequacy in vegetarians
Sources: Meat & dairy products
Congenital disorders of B12 binding proteins
Vitamin B12 R-binding protein deficiency
.....Neurological B12 deficiency syndromes in adults
Gastric intrinsic factor deficiency
.....Congenital anemia & jaundice
Transcobolamin II deficiency
.....Megaloblastic anemia; Diarrhea; Immunodeficiency; Mental retardation
Abnormalities of synthesis of active forms of B12
Methylcobalamin deficiency, types E and G
.....Neurological (CNS) & hematological B12 deficiency syndromes
.....In children
Adenosylcobalamin deficiency
.....Episodic ketoacidosis; Encephalopathy; Neutropenia; Osteoporosis
Combined methylcobalamin & adenosylcobalamin deficiency
.....Types I and II
.....Mental retardation; anemia; ± myelopathy in slowly progressive cases
Nitrous oxide exposure
.....Oxidizes cobalt in cobolamin: Methylcobalamin inactivated
.....Inhibits conversion of homocysteine to methionine:
.....Reduced supply of S-adenosylmethionine
Abnormal release of B12 from lysosomes
ps i just had to edit a mistake in my d3 labwork post. in case you had already printed it, here is the correction
pps i used to faint as a child too!the main points are, take D3 not D2, and when you are having bloodwork done, the lab requisition should say 25(OH)vitaminD3 (or equivalent, i.e. 25-hydroxycholecalciferol. NOT 1,25 dihydroxycholecalciferol).
- conandcait
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