Skip to main content
Top
Published in: The Egyptian Journal of Neurology, Psychiatry and Neurosurgery 1/2021

Open Access 01-12-2021 | Multiple Sclerosis | Research

Prevalence of antinuclear antibody in patients with multiple sclerosis: a case-control study

Authors: Hind Alnajashi, Foziah Alshamrani

Published in: The Egyptian Journal of Neurology, Psychiatry and Neurosurgery | Issue 1/2021

Login to get access

Abstract

Background

Antinuclear antibody (ANA) is a common test for excluding alternative diagnoses. However, the significance of ANA testing in patients with multiple sclerosis (MS) remains unclear.

Objectives

To compare the prevalence of positive ANA antibody and its titer between patients with MS (cases) and non-MS patients who attended neurology clinics (control) in Saudi Arabia.

Methods

A case-control review of ANA results for all patients who attended a neurology MS clinic. We compared a convenience sample of patients with MS with individuals with general neurology problems and no known autoimmune diseases.

Results

There were 115 and 103 participants in the MS and control group, respectively. The mean age in the MS and control group was 33.76 ± 8.96 years and 34.95 ± 8.56 years, respectively. In the MS group, 25.22%, 60%, 11.30%, and 3.48% were negative, mildly positive, moderately positive, and strongly positive for ANA, respectively. In the control group, there were 34.95%, 54.37%, and 10.68% were negative, mild positive, and moderate positive, respectively. There were numerically, but not significantly, more positive cases in the MS group (74.78%) than in the control group (65.05%) (p = .117).

Conclusion

ANA testing in routine MS screening for excluding alternative diagnoses should be discouraged unless there is a remarkable history or clinical examination finding. Mild positive ANA is common among patients with MS and does not significantly differ from the general population.
Literature
1.
go back to reference Aktas O, Wattjes MP, Stangel M, Hartung HP. Diagnosis of multiple sclerosis: revision of the McDonald criteria 2017. Nervenarzt. 2018 ;89(12). Aktas O, Wattjes MP, Stangel M, Hartung HP. Diagnosis of multiple sclerosis: revision of the McDonald criteria 2017. Nervenarzt. 2018 ;89(12).
2.
go back to reference Calabrese M, Gasperini C, Tortorella C, Schiavi G, Frisullo G, Ragonese P, et al. “Better explanations” in multiple sclerosis diagnostic workup: a 3-year longitudinal study. Neurology. 2019;92(22). Calabrese M, Gasperini C, Tortorella C, Schiavi G, Frisullo G, Ragonese P, et al. “Better explanations” in multiple sclerosis diagnostic workup: a 3-year longitudinal study. Neurology. 2019;92(22).
3.
go back to reference Fatemi G, Kermani TA. Clinical significance of a positive antinuclear antibody test. JAMA.2015;314(8). Fatemi G, Kermani TA. Clinical significance of a positive antinuclear antibody test. JAMA.2015;314(8).
4.
go back to reference Bernardini S, Infantino M, Bellincampi L, Nuccetelli M, Afeltra A, Lori R, et al. Screening of antinuclear antibodies: comparison between enzyme immunoassay based on nuclear homogenates, purified or recombinant antigens and immunofluorescence assay. Clin Chem Lab Med. 2004;42(10). Bernardini S, Infantino M, Bellincampi L, Nuccetelli M, Afeltra A, Lori R, et al. Screening of antinuclear antibodies: comparison between enzyme immunoassay based on nuclear homogenates, purified or recombinant antigens and immunofluorescence assay. Clin Chem Lab Med. 2004;42(10).
5.
go back to reference Marin GG, Cardiel MH, Cornejo H, Viveros ME. Prevalence of antinuclear antibodies in 3 groups of healthy individuals: blood donors, hospital personnel, and relatives of patients with autoimmune diseases. J Clin Rheumatol. 2009;15(7) Marin GG, Cardiel MH, Cornejo H, Viveros ME. Prevalence of antinuclear antibodies in 3 groups of healthy individuals: blood donors, hospital personnel, and relatives of patients with autoimmune diseases. J Clin Rheumatol. 2009;15(7)
6.
go back to reference Abeles AM, Abeles M. The clinical utility of a positive antinuclear antibody. AJM. 2013;126(4).. Abeles AM, Abeles M. The clinical utility of a positive antinuclear antibody. AJM. 2013;126(4)..
7.
go back to reference Tourbah A, Clapin A, Gout O, Fontaine B, Liblau R, Batteux F, et al. Systemic autoimmune features and multiple sclerosis: a 5-year follow-up study. Arch Neurol 1998;55(4). Tourbah A, Clapin A, Gout O, Fontaine B, Liblau R, Batteux F, et al. Systemic autoimmune features and multiple sclerosis: a 5-year follow-up study. Arch Neurol 1998;55(4).
8.
go back to reference Dal-Bianco A, Wenhoda F, Rommer PS, Weber M, Altmann P, Kraus J, et al. Do elevated autoantibodies in patients with multiple sclerosis matter? Acta Neurol Scand. 2019;139(3). Dal-Bianco A, Wenhoda F, Rommer PS, Weber M, Altmann P, Kraus J, et al. Do elevated autoantibodies in patients with multiple sclerosis matter? Acta Neurol Scand. 2019;139(3).
9.
go back to reference Series C. A challenging entity: multiple sclerosis or collagen tissue disorders: a case series of 6 patients. Caspian J Intern Med. 2017;8(4). Series C. A challenging entity: multiple sclerosis or collagen tissue disorders: a case series of 6 patients. Caspian J Intern Med. 2017;8(4).
10.
go back to reference Satoh M, Chan EKL, Ho LA, Rose KM, Parks CG, Cohn RD, et al. Prevalence and sociodemographic correlates of antinuclear antibodies in the United States. Arthritis Rheum 2012;64(7). Satoh M, Chan EKL, Ho LA, Rose KM, Parks CG, Cohn RD, et al. Prevalence and sociodemographic correlates of antinuclear antibodies in the United States. Arthritis Rheum 2012;64(7).
11.
go back to reference Lang K, Prüss H. Frequencies of neuronal autoantibodies in healthy controls. Neurol - Neuroimmunol Neuroinflammation. 2017;4(5). Lang K, Prüss H. Frequencies of neuronal autoantibodies in healthy controls. Neurol - Neuroimmunol Neuroinflammation. 2017;4(5).
12.
go back to reference Van der Vuurst de Vries RM, Mescheriakova JY, Wong YYM, Runia TF, Jafari N, Samijn JP, et al. Application of the 2017 revised mcdonald criteria for multiple sclerosis to patients with a typical clinically isolated syndrome. JAMA Neurol. 2018 1;75(11) Van der Vuurst de Vries RM, Mescheriakova JY, Wong YYM, Runia TF, Jafari N, Samijn JP, et al. Application of the 2017 revised mcdonald criteria for multiple sclerosis to patients with a typical clinically isolated syndrome. JAMA Neurol. 2018 1;75(11)
13.
go back to reference Tintore M, Rovira À, Río J, Otero-Romero S, Arrambide G, Tur C, et al. Defining high, medium and low impact prognostic factors for developing multiple sclerosis. Brain. 2015;138(7). Tintore M, Rovira À, Río J, Otero-Romero S, Arrambide G, Tur C, et al. Defining high, medium and low impact prognostic factors for developing multiple sclerosis. Brain. 2015;138(7).
14.
go back to reference van der Kaaden AJ, Kamphuis DJ, Nossent JC, Rico RE. Longstanding isolated cerebral systemic lupus erythematosus in an 8-year-old black girl. Resemblance with multiple sclerosis. Clin Neurol Neurosurg. 1993;95(3). van der Kaaden AJ, Kamphuis DJ, Nossent JC, Rico RE. Longstanding isolated cerebral systemic lupus erythematosus in an 8-year-old black girl. Resemblance with multiple sclerosis. Clin Neurol Neurosurg. 1993;95(3).
Metadata
Title
Prevalence of antinuclear antibody in patients with multiple sclerosis: a case-control study
Authors
Hind Alnajashi
Foziah Alshamrani
Publication date
01-12-2021
Publisher
Springer Berlin Heidelberg
DOI
https://doi.org/10.1186/s41983-021-00284-6

Other articles of this Issue 1/2021

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery 1/2021 Go to the issue