Levels of brain-derived neurotrophic factor in patients with multiple sclerosis

被引:27
作者
Naegelin, Yvonne [1 ,2 ,3 ,4 ,5 ]
Saeuberli, Katharina [5 ]
Schaedelin, Sabine [6 ]
Dingsdale, Hayley [5 ]
Magon, Stefano [1 ,2 ,3 ,4 ,7 ]
Baranzini, Sergio [8 ]
Amann, Michael [9 ,10 ]
Parmar, Katrin [1 ,2 ,3 ,4 ,9 ]
Tsagkas, Charidimos [1 ,2 ,3 ,4 ,9 ]
Calabrese, Pasquale [1 ,2 ,3 ,4 ,11 ]
Penner, Iris Katharina [12 ]
Kappos, Ludwig [1 ,2 ,3 ,4 ]
Barde, Yves-Alain [5 ]
机构
[1] Univ Hosp Basel, Dept Med, Neurol Clin & Policlin, CH-4031 Basel, Switzerland
[2] Univ Hosp Basel, Dept Clin Res, Neurol Clin & Policlin, CH-4031 Basel, Switzerland
[3] Univ Hosp Basel, Dept Biomed & Biomed Engn, Neurol Clin & Policlin, CH-4031 Basel, Switzerland
[4] Univ Basel, CH-4031 Basel, Switzerland
[5] Cardiff Univ, Sch Biosci, Cardiff CF10 3AX, Wales
[6] Univ Hosp Basel, Dept Clin Res, Clin Trial Unit, CH-4031 Basel, Switzerland
[7] F Hoffmann La Roche Ltd, Roche Innovat Ctr Basel, Pharma Res & Early Dev, CH-4058 Basel, Switzerland
[8] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94158 USA
[9] Med Image Anal Ctr MIAC AG, CH-4051 Basel, Switzerland
[10] Univ Basel, Dept Biomed Engn, CH-4123 Allschwil, Switzerland
[11] Univ Basel, Dept Psychol, Div Mol & Cognit Neurosci, CH-4055 Basel, Switzerland
[12] Heinrich Heine Univ Dusseldorf, Med Fac, Dept Neurol, D-40225 Dusseldorf, Germany
关键词
SERUM BDNF LEVELS; VAL66MET POLYMORPHISM; IMMUNE; INFLAMMATION; ASSOCIATION; SECRETION; PLATELET; DISEASE; LESIONS; CELLS;
D O I
10.1002/acn3.51215
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To determine the levels of brain-derived neurotrophic factor (BDNF) in the serum of patients suffering from multiple sclerosis (MS) to evaluate the potential of serum BDNF as a biomarker for MS. Methods: Using a recently validated enzyme-linked immunoassay (ELISA) we measured BDNF in patients with MS (pwMS), diagnosed according to the 2001 McDonald criteria and aged between 18 and 70 years, participating in a long-term cohort study with annual clinical visits, including blood sampling, neuropsychological testing, and brain magnetic resonance imaging (MRI). The results were compared with an age- and sex-matched cohort of healthy controls (HC). Correlations between BDNF levels and a range of clinical and magnetic resonance imaging variables were assessed using an adjusted linear model. Results: In total, 259 pwMS and 259 HC were included, with a mean age of 44.42 +/- 11.06 and 44.31 +/- 11.26 years respectively. Eleven had a clinically isolated syndrome (CIS), 178 relapsing remitting MS (RRMS), 56 secondary progressive MS (SPMS), and 14 primary progressive MS (PPMS). Compared with controls, mean BDNF levels were lower by 8 % (p<0.001) in pwMS. The level of BDNF in patients with SPMS was lower than in RRMS (p = 0.004). Interpretation: We conclude that while the use of comparatively large cohorts enables the detection of a significant difference in BDNF levels between pwMS and HC, the difference is small and unlikely to usefully inform decision-making processes at an individual patient level.
引用
收藏
页码:2251 / 2261
页数:11
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