Although anti-myelin-associated glycoprotein (MAG) antibody neuropathy is reported as a slowly progressive disease, it can lead to significant disability and impairment of health related quality of life (HR-QoL) and social participation. The aim of this crosssectional study was to evaluate the functioning and HR-QoL determinants in 67 patients with anti-MAG neuropathy in terms of the International Classification of Functioning, Disability, and Health (ICF). Evaluations included: Medical Research Council (MRC) sum score, Sensory Modality Sum score (SMS), Berg balance scale (BBS), Fatigue Severity Scale (FSS), Visual Analogue Scale (VAS) for pain, 9-Hole Peg Test (9-HPT), 6-Minute Walk Distance (6MWD), Impact on Participation and Autonomy (IPA) and the physical component score (PCS) and mental component score (MCS) of the short-form-36 health status scale (SF-36) HR-QoL measure. In the regression models, 6MWD was the most reliable predictor of PCS, explaining the 52% of its variance, while the strongest determinants of 6MWD were BBS and FSS, explaining the 41% of its variance. Consistently, VAS and BBS were good predictor of PCS, explaining together 54% of its variance. FSS was the most reliable determinant of MCS, explaining 25% of its variance. SMS and MRC were not QoL determinants. The results of our study suggest that 6MWD and FSS might be considered as potential meaningful outcome measures in future clinical trials. Furthermore, neurorehabilitation interventions aimed at improving balance and walking performance, fatigue management, and specific pain relief therapy should be considered in order to ameliorate participation in social life and HR-QoL in anti-MAG neuropathy patients.

Functioning and quality of life in patients with neuropathy associated with anti-MAG antibodies / Y. Falzone, M. Campagnolo, M. Bianco, P. Dacci, D. Martinelli, M. Ruiz, S. Bocci, F. Cerri, A. Quattrini, G. Comi, L. Benedetti, F. Giannini, G. Lauria, E. Nobile-Orazio, C. Briani, R. Fazio, N. Riva. - In: JOURNAL OF NEUROLOGY. - ISSN 0340-5354. - 265:12(2018 Dec 01), pp. 2927-2933. [10.1007/s00415-018-9081-7]

Functioning and quality of life in patients with neuropathy associated with anti-MAG antibodies

G. Lauria;E. Nobile-Orazio
Writing – Review & Editing
;
2018

Abstract

Although anti-myelin-associated glycoprotein (MAG) antibody neuropathy is reported as a slowly progressive disease, it can lead to significant disability and impairment of health related quality of life (HR-QoL) and social participation. The aim of this crosssectional study was to evaluate the functioning and HR-QoL determinants in 67 patients with anti-MAG neuropathy in terms of the International Classification of Functioning, Disability, and Health (ICF). Evaluations included: Medical Research Council (MRC) sum score, Sensory Modality Sum score (SMS), Berg balance scale (BBS), Fatigue Severity Scale (FSS), Visual Analogue Scale (VAS) for pain, 9-Hole Peg Test (9-HPT), 6-Minute Walk Distance (6MWD), Impact on Participation and Autonomy (IPA) and the physical component score (PCS) and mental component score (MCS) of the short-form-36 health status scale (SF-36) HR-QoL measure. In the regression models, 6MWD was the most reliable predictor of PCS, explaining the 52% of its variance, while the strongest determinants of 6MWD were BBS and FSS, explaining the 41% of its variance. Consistently, VAS and BBS were good predictor of PCS, explaining together 54% of its variance. FSS was the most reliable determinant of MCS, explaining 25% of its variance. SMS and MRC were not QoL determinants. The results of our study suggest that 6MWD and FSS might be considered as potential meaningful outcome measures in future clinical trials. Furthermore, neurorehabilitation interventions aimed at improving balance and walking performance, fatigue management, and specific pain relief therapy should be considered in order to ameliorate participation in social life and HR-QoL in anti-MAG neuropathy patients.
Chronic inflammatory polyneuropathy, pain, MGUS, rehabilitation, walking ability, balance
Settore MED/26 - Neurologia
1-dic-2018
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/597094
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