Patient: Female, 49
Final Diagnosis: Myasthenia Gris
Symptoms: Muscle weakness • shortness of breath
Medication: —
Clinical Procedure: Vitamin D
Specialty: Endocrinology and Metabolic
Objective:Unusual or unexpected effect of treatment
Background:Vitamin D has been shown to be related to autoimmune diseases, such as multiple sclerosis and psoriasis. Correlations he been reported between vitamin D levels and prevalence and severity of other autoimmune disorders, and also between vitamin D therapy and disease improvement and remission.
Case Report:This is a case report of a patient with severe and refractory myasthenia gris (MG) who followed a “high-dose vitamin D treatment”, a massive-dose treatment (80 000 to 120 000 IU/day) promoted by a medical center in Brazil (but still not proven), and she had her first complete remission after this type of treatment with increased vitamin D serum levels (400 to 700 ng/mL).
Conclusions:This case report may reinforce the reported correlation between vitamin D level and disease severity and introduces a possible new use for vitamin D as a potential target for treating autoimmune diseases. We recommend large, double-blind, placebo-controlled, randomized studies using high-dose vitamin D treatment for refractory autoimmune diseases to reliably assess this pharmacotherapy target for these diseases.
MeSH Keywords: Myasthenia gris; Myasthenia gris, Autoimmune, Experimental; Vitamin D
BackgroundVitamin D has been linked in different ways to multiple autoimmune diseases. Herein, correlations were found between vitamin D levels and disease severity [1–5], incidence [2–5], and higher-dose vitamin D usage and illnesses improvement or remission [6]. In multiple sclerosis, besides all these correlations, lower vitamin D levels are also associated with relapse [4]. Vitamin D is actually a true hormone by definition, with a cytosolic receptor that acts in gene transcriptions and silencing. It has been shown to play a role in immune system modulation [7–15]. We performed a PubMed literature search on vitamin D and myasthenia gris (MG) and found only 3 articles. A pilot study showed a correlation between lower serum vitamin D levels and MG prevalence, as well as autoimmune marker decrease and fatigue improvement after vitamin D3 supplementation with 800 IU/day [6], and 2 other studies demonstrated the role of vitamin D role in the immune system in MG triggering [7] and suppression [8].
Case ReportA 49-year-old woman had a diagnosis of MG in 2008 after presenting clinical symptoms of severe and progressive muscle weakness and compromising respiratory muscles support, which led to intubation at an Intensive Care Unit and she was classified as Class V according to the Myasthenia Gris Foundation of America Clinic Classification. Between 2008 and 2013 she had some improvements after specific treatments for MG, including corticosteroid, azathioprine, pyridostigmine, and thymectomy (surgery in 2009). The lowest doses she had been taking until 2013 were prednisone daily intercalation of 20 mg and 5 mg, azathioprine 200 mg/day, and a daily dose of 120 mg pyridostigmine. She had never had complete remission of MG symptoms, even with higher doses of medications, such as daily intake of 80 mg of prednisone and 720 mg of pyridostigmine. Moreover, she experienced several episodes of disease relapse, with critical muscle symptoms worsening and continuous breathlessness.
Unsatisfied with her refractory clinical status, she decided to look for “alternative” treatments, and looked for a physician who would administer high-dose vitamin D treatment as a “potential treatment for vitamin D in autoimmune diseases”. In April of 2013, she started to take 80 000 IU/day of vitamin D and to consume a calcium-free diet to prevent hypercalcemia. She did not stop taking any of her medications at the time she started taking massive doses of vitamin D, which means that she did not replace the proven and well-established treatments with an experimental one.
She started to he significant improvements in fatigue and in muscle weakness, and became asymptomatic for the first time since she was diagnosed. She decreased her medication doses, followed by a neurologist, and was able to suspend pyridostigmine and to decrease prednisone to 10 mg/5 mg every other day and decrease azathioprine to 100 mg. Also, her anti-acetylcholine receptor (AChR) antibodies decreased from 7.40 nMol/L to 2.68 nMol/L (normal range: