Systemic AutoImmune Features & Multiple Sclerosis:
A 5-Year Follow-Up Study

Ayman Tourbah, MD, PhD; Alexis Clapin, MD; Olivier Gout, MD; Bertrand Fontaine, MD, PhD; Roland Liblau, MD, PhD; Frederic Batteux, MD; Jean-Louis Stiévenart, MD; Bernard Weill, MD, PhD; Catherine Lubetzki, MD, PhD; Olivier Lyon-Caen, MD
Arch Neurol May 1998;55:517-521

PMID# 9561980

To evaluate in patients with Multiple Sclerosis (MS) the occurrence of Clinical Systemic Signs and Biological AutoImmune abnormalities, including positive Titers of AntiNuclear AntiBodies and AntiPhospholipid AntiBodiesAntiBodies, suggestive of AutoImmune Diseases that may affect the Central Nervous System.

Also, to compare the clinical and Magnetic Resonance Imaging features and evolution of MS in patients with and without AutoImmune abnormalities.

Design and Patients
Prospective study of 161 patients fulfilling the criteria of having Probable or Definite MS hospitalized in our institution between November 1990 and June 1992.

Among the 161 patients, 84 (52.1%) had at least 1 clinical and/or biological general sign suggestive of an AutoImmune Disease; 64 were followed up for 4 to 5 years. The diagnosis of MS was confirmed in 50 patients and is still pending in 14 of them.

No significant difference was found between patients with MS who were free of AutoImmune features.

And, those with AutoImmune abnormalities (MS plus) concerning the age of disease onset, the presenting symptoms and signs, symptoms found on Neurologic Examination, and the course of the disease.

For all patients with confirmed MS, general signs were found in 13.3%, positive Titers of AntiNuclear AntiBodies in 26%, and positive Titers of AntiPhospholipid AntiBodies in 6.2%.

Patients with MS with AutoImmune features, including those with Titers of AntiNuclear AntiBodies of 1:100 or less and/or AntiPhospholipid AntiBodies, are not different than others with MS, and therefore should not be excluded from clinical trials.

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