Official Journal Health Science of Prince of Songkla University

  • Home
  • Search
  • Current
  • Archives
  • Announcements
  • Guide for Authors
  • Publication Ethics
  • Editorial Board
  • Submit
  • About
  • Contact
  • Online-first Articles
  • EVENTS
  • Review Process
Home > Vol 39, No 2 (2021) > Khanittanuphong

Acute Reversible Motor Predominant Polyradiculoneuropathy among Thai Prisoners after the Outbreak of H3N2 Influenza: A Case Series

Phichamon Khanittanuphong, Thanyalak Amornpojnimman, Sirichai Cheewatanakornkul, Watchara Viratyaporn, Ittipon Preechawettayakul, Chorfa Buntong, Pat Korathanakhun, Erin Kathleen O’Ferrall

Abstract

Objective: This study aims to describe the clinical, laboratory and electrophysiological findings of the prisoners who developed acute reversible motor predominant polyradiculoneuropathy after the outbreak of H3N2 influenza.
Material and Methods: Among H3N2 infected Thai prisoners, all patients with acute flaccid weakness were included in this retrospective case series. We analyzed the results of electromyography (EMG), cerebrospinal fluid analysis, and serum levels of antiganglioside antibodies, folate, thiamine, and vitamin B12.
Results: Among 262 H3N2 influenza patients, motor predominant polyradiculoneuropathy predominantly affecting the lower limbs developed in 10 patients. EMG revealed significantly decreased compound muscle action potentials with preserved distal latencies and conduction velocities in the peroneal nerves. Early fibrillation potentials were demonstrated on EMG performed 12-14 days post-onset of symptoms. The cerebrospinal fluid study showed normal profiles. All laboratory results appeared normal except for the significantly low mean±standard deviation serum folate level of 1.80± 0.78 [reference value 3.89–26.80 nanograms per milliliter (ng/mL)] as compared to the mean serum folate level in the normal Thai population of 10.80 ng/mL (p-value<0.001, 95% confidential interval -9.55 to -8.45). All patients were treated with 15 milligram per day of folic acid and all patients improved clinically.
Conclusion: Although the relationship between low plasma folate level and polyradiculoneuropathy is unclear, a superimposed folate deficiency contributing to the pathophysiology is possible.

 Keywords

folate deficiency; H3N2; influenza; polyradiculoneuropathy

 Full Text:

PDF

References

Marx A, Glass JD, Sutter RW. Differential diagnosis of acute flaccid paralysis and its role in poliomyelitis surveillance. Epidemiol Rev 2000;22:298-316.

Areekul S, Cheeramakara C, Churdchu K, Pongpaew P, Suwanbun N. Serum folate and vitamin B12 levels in chronic alcoholics. Siriraj Hosp Gaz 1993;45:14-8.

Zeng Y, Liu Y, Xie Y, Liang J, Xiao Z, Lu Z. Clinical Features and the validation of the brighton criteria in Guillain-Barré syndrome: retrospective analysis of 72 hospitalized patients in three years. Eur Neurol 2019;1:1-8.

Willison HJ, Goodyear CS. Glycolipid antigens and autoantibodies in autoimmune neuropathies. Trends Immunol 2013;34:453–9.

Jacobs BC, Rothbarth PH, van der Meché FG, Herbrink P, Schmitz PI, de Klerk MA, et al. The spectrum of antecedent infections in Guillain-Barré syndrome: a case-control study. Neurology 1998;51:1110–5.

Paploski IA, Prates AP, Cardoso CW, Kikuti M, Silva MM, Waller LA, et al. Time lags between exanthematous illness attributed to Zika Virus, Guillain-Barré syndrome, and microcephaly, Salvador, Brazil. Emerg Infect Dis 2016;22:1438- 44.

Kwong JC, Vasa PP, Campitelli MA, Hawken S, Wilson K, Rosella LC, et al. Risk of Guillain-Barré syndrome after seasonal influenza vaccination and influenza health-care encounters: a self-controlled study. Lancet Infect Dis 2013; 13:769-76.

Dumitru D, King JC. Fibrillation potential amplitude after denervation. Am J Phys Med Rehabil 1998;77:483-9.

Koike H, Takahashi M, Ohyama K, Hashimoto R, Kawagashira Y, Iijima M, et al. Clinicopathologic features of folate-deficiency neuropathy. Neurology 2015;84:1026-33.

Botez MI, Peyronnard JM, Bachevalier J, Charron L. Polyneuropathy and folate deficiency. Arch Neurol 1978;35:581-4.

Koike H, Hama T, Kawagashira Y, Hashimoto R, Tomita M, Iijima M, et al. The significance of folate deficiency in alcoholic and nutritional neuropathies: analysis of a case. Nutrition 2012;28:821-4.

Kreijtz JH, Fouchier RA, Rimmelzwaan GF. Immune responses to influenza virus infection.Virus Res 2011;162:19-30.

Xia W, Hilgenbrink AR, Matteson EL, Lockwood MB, Cheng JX, Low PS. A functional folate receptor is induced during macrophage activation and can be used to target drugs to activated macrophages. Blood 2009;113:438-46.

Yi YS. Folate receptor-targeted diagnostics and therapeutics for inflammatory diseases. Immune Netw 2016;16:337- 43.

Osifo BO, Lukanmbi FA, Familusi JB. Increase of body temperature and folic acid metabolism. Acta Vitaminol Enzymol 1981;3:177-81.

DOI: http://dx.doi.org/10.31584/jhsmr.2020769

Refbacks

  • There are currently no refbacks.
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

SUBMIT A PAPER

JHSMR accepts online submission through

AHR-iCON 2024

Journal Metrics


2020
Acceptance rate: 52%
2021
Acceptance rate: 27.8%
2022 (March)
Acceptance rate: 15.6%
2023 (June)
Acceptance rate: 23.6%
2024 (June)
Acceptance rate: 19%


Submission to final decision
74 days

Acceptance to publication
40 days

SCImago Journal & Country Rank

About The Authors

Phichamon Khanittanuphong
Department of Rehabilitation Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla 90110,
Thailand

Thanyalak Amornpojnimman
Neurology Unit, Department of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla 90110,
Thailand

Sirichai Cheewatanakornkul
Cadiology Unit, Department of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla 90110,
Thailand

Watchara Viratyaporn
Department of Internal Medicine, Hatyai Hospital, Hat Yai, Songkhla 90110,
Thailand

Ittipon Preechawettayakul
Department of Internal Medicine, Na-Thawi Hospital, Na-Thawi, Songkhla 90160,
Thailand

Chorfa Buntong
Nursing Unit, Na-Thawi District Prison, Na-Thawi, Songkhla 90160,
Thailand

Pat Korathanakhun
Departments of Neurology and Neurosurgery, Faculty of Medicine, McGill University, Montréal Neurological Institute and Hospital, Montréal, Québec H3A 2B4,
Canada

Erin Kathleen O’Ferrall
Departments of Neurology and Neurosurgery, Faculty of Medicine, McGill University, Montréal Neurological Institute and Hospital, Montréal, Québec H3A 2B4, Canada. Department of Pathology, Faculty of Medicine, McGill University, Montréal Neurological Institute and Hospital, Montréal, Québec H3A 2B4,
Canada

Article Tools
Abstract
Print this article
Indexing metadata
How to cite item
Email this article (Login required)
Email the author (Login required)

Supported by

 

JHSMR now Indexed in



Scopus logo.svg






Image result for crossref





PSUMJ Homepage

Keywords COVID-19 SARS-CoV-2 Thailand anxiety children computed tomography depression diabetes diabetes mellitus elderly hypertension knowledge mental health mortality prevalence quality of life reliability risk factor risk factors treatment validity
Journal Content

Browse
  • By Issue
  • By Author
  • By Title
Font Size

Open Journal Systems