Long-Term Follow-Up of 106 Multiple Sclerosis Patients Undergoing Interferon-β 1a or 1b Therapy: Predictive Factors of Thyroid Disease Development and Duration

Author:

Caraccio N.1,Dardano A.1,Manfredonia F.2,Manca L.2,Pasquali L.2,Iudice A.2,Murri L.2,Ferrannini E.1,Monzani F.1

Affiliation:

1. Departments of Internal Medicine (N.C., A.D., E.F., F.Mo.), 56126 Pisa, Italy

2. Neuroscience (F.Ma., L.Ma., L.P., A.I., L.Mu.), University of Pisa, 56126 Pisa, Italy

Abstract

Abstract Background: Conflicting data have been reported on the association between interferon (IFN)-β therapy of multiple sclerosis (MS) patients and thyroid disease development. Aims: The goals of this study are as follows: to assess the actual occurrence of thyroid dysfunction and autoimmunity during long-term IFN-β therapy; to establish the possible presence of predictive factors for thyroid dysfunction development and duration; and to suggest an effective follow-up protocol for patients receiving long-term IFN-β therapy. Study Protocol: A total of 106 MS patients (76 women) underwent IFN-β 1a or 1b therapy for up to 84 months (median, 42 months). Thyroid function and autoimmunity were assessed at baseline and every 3–6 months throughout the treatment course. Results: Baseline thyroid autoimmunity was detected in 8.5% of patients and hypothyroidism in 2.8%. Thyroid dysfunction (80% hypothyroidism, 92% subclinical, 56% transient) developed in 24% (68% with autoimmunity) of patients and autoimmunity in 22.7% (45.5% with dysfunction), without significant differences between the two cytokines; 68% of dysfunctions occurred within the first year. Autoimmunity emerged as the only predictive factor for dysfunction development (relative risk, 8.9), whereas sustained disease was significantly associated with male gender (P < 0.003). Conclusions: Both incident thyroid autoimmunity and dysfunction frequently occur in MS patients during IFN-β therapy, particularly within the first year of treatment. Thyroid dysfunction is generally subclinical and transient in over than half of cases; preexisting or incident autoimmunity emerged as the only significant predictive factor for thyroid dysfunction development. Thyroid function and autoimmunity assessment is mandatory within the first year of IFN-β therapy; thereafter, serum TSH measurement only in patients with thyroid disease could be sufficient.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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