| Literature DB >> 31473879 |
Wildéa Lice de Carvalho Jennings Pereira1,2, Tamires Flauzino1, Daniela Frizon Alfieri1, Sayonara Rangel Oliveira1,3, Ana Paula Kallaur1, Andrea Name Colado Simão1,3, Marcell Alysson Batisti Lozovoy1,3, Damacio Ramón Kaimen-Maciel2,4, Michael Maes5,6, Edna Maria Vissoci Reiche7,8.
Abstract
An association between prolactinemia with disability, clinical forms, and sex of patients with multiple sclerosis (MS) remains unclear. The aim of this study was to evaluate the association of prolactin with clinical forms and accumulating disability over time in patients with MS. A longitudinal study was carried out with 101 patients with relapsing-remitting MS (RRMS) and 19 with progressive forms of MS (ProgMS). The disability over time, as well as prolactin and ferritin serum levels were evaluated at baseline (T0), 8-month follow-up (T8), and 16-month follow-up. The disability at T0, T8, and T16 was higher among patients with ProgMS than those with RRMS. Prolactin and ferritin levels did not differ over time between both groups. Initially, prolactin was associated with MS disability. After introducing age and sex, the effects of prolactin on disability were no longer significant. Prolactin was associated with age and sex, whereby age was positively associated with disability. In the same way, after introducing age and sex, the effects of diagnosis on prolactin levels, as well as the association between prolactin and ferritin, were no longer significant (P = 0.563 and P = 0.599, respectively). Moreover, 21.6% of the variance in the disability was predicted by age (P < 0.001), and sex (P = 0.049), while prolactin was not significant. In conclusion, the effects of prolactin on the disability and clinical forms of MS patients may be spurious results because those correlations reflect the positive associations of age with the disability and the negative association of age with prolactin.Entities:
Keywords: Disability; Ferritin; Multiple sclerosis; Prolactin; Spurious result
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Year: 2019 PMID: 31473879 DOI: 10.1007/s12017-019-08565-3
Source DB: PubMed Journal: Neuromolecular Med ISSN: 1535-1084 Impact factor: 3.843