A randomised clinical trial comparing interferon-alpha and intravenous immunoglobulin in polyneuropathy associated with monoclonal IgM. The IgM-associated Polyneuropathy Study Group.

Abstract

OBJECTIVES:

The polyneuropathy associated with a monoclonal IgM directed to the myelin associated glycoprotein (MAG) is a specific entity with a putative causal link between the IgM and the neuropathy. The small benefit offered by alkylating agents or plasma exchanges in these patients justifies the search for alternative treatments.

METHODS:

A 12 month multicentre, prospective, randomised, open clinical trial was carried out comparing intravenous immunoglobulin (IVIg; 2g/kg and then 1 g/kg every three weeks) and recombinant interferon-alpha (IFN-alpha; 3 MU/m2 subcutaneously three times weekly). The main end point was a clinical neuropathy disability score (CNDS) after six months of treatment. Twenty patients were enrolled; 10 were assigned to IVIg and 10 to IFN-alpha.

RESULTS:

At six months, one out of 10 patients treated with IVIg had a CNDS improvement of more than 20% whereas eight out of 10 patients treated with IFN-alpha had such an improvement (P=0.005). The mean CNDS worsened by 2.3 (SD 7.6) (8%) in the IVIg group whereas it improved by 7.5 (SD 11.1) (31%) in the IFN-alpha group (P=0.02). This improvement persisted after 12 months and was mainly related to an improvement of the sensory component (P=0.02) whereas the motor component was unchanged (P=0.39). Electrophysiological data did not show improvement of motor nerve conduction velocities whereas sensory nerve conduction velocities improved in the upper limbs. A decrease in the level of the monoclonal IgM was seen in two patients treated with IFN-alpha. At the end of the treatment, antibody activity to MAG was still detected in the serum of all patients.

CONCLUSION:

IVIg, as used in this study, did not improve patients with polyneuropathy and monoclonal IgM. By contrast, although its mechanism of action remains to be fully elucidated, IFN-alpha was effective in eight out of 10 patients at six months.

• Authors: X Mariette, C Chastang, P Clavelou, J P Louboutin, J M Leger, J C Brouet
• Journal: Journal of neurology, neurosurgery, and psychiatry (J Neurol Neurosurg Psychiatry) Vol. 63 Issue 1 Pg. 28-34 (Jul 1997) ISSN: 0022-3050 [Print] England
• PMID: 9221964 (Publication Type: Clinical Trial, Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)

Chemical References

• Immunoglobulin M
• Immunoglobulins, Intravenous
• Interferon Type I
• Myelin-Associated Glycoprotein
• Recombinant Proteins

Topics

• Adult
• Aged
• Electrophysiology
• Female
• Humans
• Immunoglobulin M (immunology)
• Immunoglobulins, Intravenous (therapeutic use)
• Interferon Type I (therapeutic use)
• Male
• Middle Aged
• Myelin-Associated Glycoprotein (immunology)
• Neural Conduction
• Paraproteinemias (therapy)
• Peripheral Nervous System Diseases (therapy)
• Recombinant Proteins
• Severity of Illness Index
• Treatment Outcome