Multiple sclerosis - Neurofilament light chain antibodies are correlated to cerebral atrophy

被引:102
作者
Eikelenboom, MJ
Petzold, A
Lazeron, RHC
Silber, E
Sharief, M
Thompson, EJ
Barkhof, F
Giovannoni, G
Polman, CH
Uitdehaag, BMJ
机构
[1] Vrije Univ Amsterdam, Ctr Med, Dept Neurol, NL-1007 MB Amsterdam, Netherlands
[2] Kings Coll London, Dept Neuroinflammat, Guys King & St Thomas Med Sch, London WC2R 2LS, England
[3] Kings Coll London, Neurol Inst, Guys Kings & St Thomas Med Sch, London WC2R 2LS, England
[4] Kings Coll London, Dept Neuroimmunol, Guys Kings & St Thomas Med Sch, London WC2R 2LS, England
关键词
D O I
10.1212/01.WNL.0000041496.58127.E3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To evaluate markers of axonal damage in CSF and serum of patients with different subtypes of MS in relation to measures of disease progression on MRI. Methods: In 51 patients with MS (21 relapsing-remitting, 20 secondary progressive, 10 primary progressive), levels of heavy and light neurofilaments (NfH and NfL) and antibodies to neurofilaments (anti-NfL and -NfH) as well as the total immunoglobulin G (IgG) were analyzed. MRI analysis included T2 hyperintense, T1 hypointense, and gadolinium enhancing lesions and markers of cerebral atrophy (ventricular and parenchymal fractions). Results: For the total group, correlations were found between the anti-NfL index and the parenchymal fraction (PF) (r = -0.51, p < 0.001), T2 lesion load (r = 0.41, p < 0.05), ventricular fraction (r = 0.37, p < 0.05), and T1 lesion load (r = 0.37, p < 0.05). For the anti-NfH index, a correlation was found with the PF (r = -0.39, p < 0.05). No correlations were found between the IgG index and MRI measures. Conclusions: Intrathecal production of anti-NfL antibodies may serve as a marker of tissue damage, particularly axonal loss, in MS.
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页码:219 / 223
页数:5
相关论文
共 29 条
  • [1] A real-time insight into disease progression and the role of axonal injury in multiple sclerosis
    Bjartmar, C
    Kidd, G
    Ransohoff, RM
    [J]. ARCHIVES OF NEUROLOGY, 2001, 58 (01) : 37 - 39
  • [2] Lesion heterogeneity in multiple sclerosis: a study of the relations between appearances on T1 weighted images, T1 relaxation times, and metabolite concentrations
    Brex, PA
    Parker, GJM
    Leary, SM
    Molyneux, PD
    Barker, GJ
    Davie, CA
    Thompson, AJ
    Miller, DH
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2000, 68 (05) : 627 - 632
  • [3] Brain atrophy in clinically early relapsing-remitting multiple sclerosis
    Chard, DT
    Griffin, CM
    Parker, GJM
    Kapoor, R
    Thompson, AJ
    Miller, DH
    [J]. BRAIN, 2002, 125 : 327 - 337
  • [4] Persistent functional deficit in multiple sclerosis and autosomal dominant cerebellar ataxia is associated with axon loss
    Davie, CA
    Barker, GJ
    Webb, S
    Tofts, PS
    Thompson, AJ
    Harding, AE
    McDonald, WI
    Miller, DH
    [J]. BRAIN, 1995, 118 : 1583 - 1592
  • [5] The natural history of multiple sclerosis
    G.C. Ebers
    [J]. Neurological Sciences, 2000, 21 (Suppl 2) : S815 - S817
  • [6] Fu L, 1996, NMR BIOMED, V9, P339, DOI 10.1002/(SICI)1099-1492(199612)9:8<339::AID-NBM422>3.0.CO
  • [7] 2-X
  • [8] A structural scaffolding of intermediate filaments in health and disease
    Fuchs, E
    Cleveland, DW
    [J]. SCIENCE, 1998, 279 (5350) : 514 - 519
  • [9] PHOSPHORYLATION PROTECTS NEUROFILAMENTS AGAINST PROTEOLYSIS
    GOLDSTEIN, ME
    STERNBERGER, NH
    STERNBERGER, LA
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1987, 14 (02) : 149 - 160
  • [10] Longitudinal brain volume measurement in multiple sclerosis - Rate of brain atrophy is independent of the disease subtype
    Kalkers, NF
    Ameziane, N
    Bot, JCJ
    Minneboo, A
    Polman, CH
    Barkhof, F
    [J]. ARCHIVES OF NEUROLOGY, 2002, 59 (10) : 1572 - 1576