Semin Neurol
DOI: 10.1055/s-0044-1791693
Mitali Mehta
1
Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York
,
Jessica Robinson-Papp
1
Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York
› Author Affiliations
Funding Dr. Robinson-Papp is supported by grants from the NIH including: R01DK122853. Dr. Robinson-Papp has received NIH grant funding to investigate HIV-associated neuropathies and diabetic neuropathic pain. Additionally, royalties have been received from UpToDate for articles on neuropathy. Speaker honoraria have been received from the American Academy of Neurology and the Clinical Education Initiative. The aforementioned NIH grants include funds for travel to academic meetings. Dr. Robinson-Papp also serves as a Scientific Advisory Board Member for Neuropathix, Inc. and Immgenuity Inc.
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Abstract
This review explores diverse infectious etiologies of peripheral nervous system (PNS) dysfunction, spanning sensory and motor neurons, nerves, and associated structures. Progress in viral and bacterial infections reveals multifaceted mechanisms underlying neuropathies, including viral neurotoxicity and immune-mediated responses. Latest diagnostic advances facilitate early PNS complication detection, with ongoing research offering promising treatment avenues. Emerging pathogens like severe acute respiratory syndrome coronavirus 2, Zika virus, and EV-D68 highlight the evolving infectious neuropathy paradigm. Recognizing characteristic patterns and integrating clinical factors are pivotal for precise diagnosis and tailored intervention. Challenges persist in assessment and management due to varied pathogenic mechanisms. Advancements in understanding pathogenesis have improved targeted therapies, yet gaps remain in effective treatments. Ongoing research is crucial for optimizing approaches and improving patient outcomes.
Keywords
peripheral neuropathies -
distal symmetrical -
sensory-predominant polyneuropathy -
HIV infection -
demyelinating neuropathy
Publication History
Article published online:
11 October 2024
© 2024. Thieme. All rights reserved.
Thieme Medical Publishers, Inc.
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References
1
Gabbai AA,
Castelo A,
Oliveira AS.
HIV peripheral neuropathy. Handb Clin Neurol 2013; 115: 515-529
2
Widyadharma IPE,
Barus J,
Dewi PR,
Yaputra F,
Adnyana IMO,
Samatra D.
Glial cells involvement in pathogenesis of human immunodeficiency virus-associated sensory neuropathy (HIV-SN): literature review. Int J Med Rev Case Rep 2018; 2 (03) 49-52
3
Roda RH,
Hoke A.
Mitochondrial dysfunction in HIV-induced peripheral neuropathy. Int Rev Neurobiol 2019; 145: 67-82
4
Cherry CL,
Wadley AL,
Kamerman PR.
Painful HIV-associated sensory neuropathy. Pain Manag (Lond) 2012; 2 (06) 543-552
5
Boustani A,
Kulbe JR,
Andalibi MS,
Pérez-Santiago J,
Mehta SR,
Ellis RJ.
et al.
Mitochondrial DNA and electron transport chain protein levels are altered in peripheral nerve tissues from donors with HIV sensory neuropathy: a pilot study. Int J Mol Sci 2024; 25 (09) 4732
6
Kranick SM,
Nath A.
Neurologic complications of HIV-1 infection and its treatment in the era of antiretroviral therapy. Continuum (Minneap Minn) 2012; 18 (6 Infectious Disease): 1319-1337
7
Peltier AC,
Russell JW.
Recent advances in drug-induced neuropathies. Curr Opin Neurol 2002; 15 (05) 633-638
8
Callaghan BC,
Price RS,
Feldman EL.
Distal symmetric polyneuropathy: a review. JAMA 2015; 314 (20) 2172-2181
9
Dimitrova A,
Murchison C,
Oken B.
Acupuncture for the treatment of peripheral neuropathy: a systematic review and meta-analysis. J Altern Complement Med 2017; 23 (03) 164-179
10
Chow D,
Nakamoto BK,
Sullivan K.
et al.
Symptoms of autonomic dysfunction in human immunodeficiency virus. Open Forum Infect Dis 2015; 2 (03) ofv103
11
Zilliox L,
Peltier AC,
Wren PA.
et al.
Assessing autonomic dysfunction in early diabetic neuropathy: the Survey of Autonomic Symptoms. Neurology 2011; 76 (12) 1099-1105
12
Robinson-Papp J,
Sharma SK.
Autonomic neuropathy in HIV is unrecognized and associated with medical morbidity. AIDS Patient Care STDs 2013; 27 (10) 539-543
13
Jiao J,
Simpson DM,
Robinson-Papp J.
HIV-Related Peripheral Nervous System Illness. New York, NY: Springer; 2017: 209-227
14
Sletten DM,
Suarez GA,
Low PA,
Mandrekar J,
Singer W.
COMPASS 31: a refined and abbreviated Composite Autonomic Symptom Score. Mayo Clin Proc 2012; 87 (12) 1196-1201
15
Steiner I.
Chapter 31 - Herpes virus infection of the peripheral nervous system. In:
Said G,
Krarup C.
eds.
Handbook of Clinical Neurology. Amsterdam, Netherlands: Elsevier; 2013: 543-558
16
Kim YS,
Hollander H.
Polyradiculopathy due to cytomegalovirus: report of two cases in which improvement occurred after prolonged therapy and review of the literature. Clin Infect Dis 1993; 17 (01) 32-37
17
Shah HA,
Meiwald A,
Perera C,
Casabona G,
Richmond P,
Jamet N.
Global prevalence of varicella-associated complications: a systematic review and meta-analysis. Infect Dis Ther 2024; 13 (01) 79-103
18
Rab SM,
Choudhury GM.
Landry-Guillain-Barre syndrome after chicken pox. N Engl J Med 1963; 268 (04) 200-201
19
Zhou J,
Li J,
Ma L,
Cao S.
Zoster sine herpete: a review. Korean J Pain 2020; 33 (03) 208-215
20
Gilden D.
Efficacy of live zoster vaccine in preventing zoster and postherpetic neuralgia. J Intern Med 2011; 269 (05) 496-506
21
Umehara T,
Sengoku R,
Mitsumura H,
Mochio S.
Neurological picture. Findings of segmental zoster paresis on MRI. J Neurol Neurosurg Psychiatry 2011; 82 (06) 694-694
22
Choi J-Y,
Kang CH,
Kim B-J,
Park K-W,
Yu S-W.
Brachial plexopathy following herpes zoster infection: two cases with MRI findings. J Neurol Sci 2009; 285 (1–2): 224-226
23
James C,
Harfouche M,
Welton NJ.
et al.
Herpes simplex virus: global infection prevalence and incidence estimates, 2016. Bull World Health Organ 2020; 98 (05) 315-329
24
Cole S.
Herpes simplex virus: epidemiology, diagnosis, and treatment. Nurs Clin North Am 2020; 55 (03) 337-345
25
Carod-Artal FJ.
Infectious diseases causing autonomic dysfunction. Clin Auton Res 2018; 28 (01) 67-81
26
Berger JR,
Houff S.
Neurological complications of herpes simplex virus type 2 infection. Arch Neurol 2008; 65 (05) 596-600
27
Handler CE,
Perkin GD.
Radiculomyelopathy due to genital herpes. Lancet 1982; 2 (8305): 987-988
28
Craig CP,
Nahmias AJ.
Different patterns of neurologic involvement with herpes simplex virus types 1 and 2: isolation of herpes simplex virus type 2 from the buffy coat of two adults with meningitis. J Infect Dis 1973; 127 (04) 365-372
29
Gilbert SC.
Bell's palsy and herpesviruses. Herpes 2002; 9 (03) 70-73
30
Neville BG,
Sladen GE.
Acute autonomic neuropathy following primary herpes simplex infection. J Neurol Neurosurg Psychiatry 1984; 47 (06) 648-650
31
Küker W,
Schaade L,
Ritter K,
Nacimiento W.
MRI follow-up of herpes simplex virus (type 1) radiculomyelitis. Neurology 1999; 52 (05) 1102-1103
32
Handley G,
Pankow S,
Bard JD,
Yee R,
Nigo M,
Hasbun R.
Distinguishing cytomegalovirus meningoencephalitis from other viral central nervous system infections. J Clin Virol 2021; 142: 104936
33
Leung J,
Sejvar JJ,
Soares J,
Lanzieri TM.
Guillain-Barré syndrome and antecedent cytomegalovirus infection, USA 2009-2015. Neurol Sci 2020; 41 (04) 885-891
34
Lefeuvre L,
Schibler M,
Lalive PH.
Elsberg syndrome secondary to cytomegalovirus infection in an immunocompetent patient. A case report. Neurol Neuroimmunol Neuroinflamm 2022; 10 (02) e200079
35
Abrantes J,
Torres DS,
Brandão-Mello CE.
The many difficulties and subtleties in the cognitive assessment of chronic hepatitis C infection. Int J Hepatol 2020; 2020: 9675235
36
Nemni R,
Sanvito L,
Quattrini A,
Santuccio G,
Camerlingo M,
Canal N.
Peripheral neuropathy in hepatitis C virus infection with and without cryoglobulinaemia. J Neurol Neurosurg Psychiatry 2003; 74 (09) 1267-1271
37
Vital C,
Vital A,
Canron MH.
et al.
Combined nerve and muscle biopsy in the diagnosis of vasculitic neuropathy. A 16-year retrospective study of 202 cases. J Peripher Nerv Syst 2006; 11 (01) 20-29
38
Adinolfi LE,
Nevola R,
Lus G.
et al.
Chronic hepatitis C virus infection and neurological and psychiatric disorders: an overview. World J Gastroenterol 2015; 21 (08) 2269-2280
39
Fornero L,
Kanouni T,
Tudesq JJ.
et al.
Preventive plasmapheresis for rituximab related flare in cryoglobulinemic vasculitis. J Transl Autoimmun 2023; 6: 100194
40
Arandjelovic S,
Bonaci-Nikolic B,
Peric-Popadic A.
et al.
HCV related severe cryoglobulinemic vasculitis treated with plasma exchange and rituximab: case report and literature review. J Infect Dev Ctries 2017; 11 (05) 431-436
41
Bureau BL,
Obeidat A,
Dhariwal MS,
Jha P.
Peripheral neuropathy as a complication of SARS-Cov-2. Cureus 2020; 12 (11) e11452
42
Gholami M,
Safari S,
Ulloa L,
Motaghinejad M.
Neuropathies and neurological dysfunction induced by coronaviruses. J Neurovirol 2021; 27 (03) 380-396
43
Iadecola C,
Anrather J,
Kamel H.
Effects of COVID-19 on the nervous system. Cell 2020; 183 (01) 16-27.e1
44
Destras G,
Bal A,
Escuret V,
Morfin F,
Lina B,
Josset L.
COVID-Diagnosis HCL Study Group.
Systematic SARS-CoV-2 screening in cerebrospinal fluid during the COVID-19 pandemic. Lancet Microbe 2020; 1 (04) e149
45
Oaklander AL,
Mills AJ,
Kelley M.
et al.
Peripheral neuropathy evaluations of patients with prolonged long COVID. Neurol Neuroimmunol Neuroinflamm 2022; 9 (03) e1146
46
Finsterer J,
Scorza FA,
Scorza C,
Fiorini A.
COVID-19 associated cranial nerve neuropathy: a systematic review. Bosn J Basic Med Sci 2022; 22 (01) 39-45
47
Abu-Rumeileh S,
Garibashvili T,
Ruf W.
et al.
Exacerbation of chronic inflammatory demyelinating polyneuropathy in concomitance with COVID-19. J Neurol Sci 2020; 418: 117106
48
Brugliera L,
Filippi M,
Del Carro U.
et al.
Nerve compression injuries after prolonged prone position ventilation in patients with SARS-CoV-2: a case series. Arch Phys Med Rehabil 2021; 102 (03) 359-362
49
Abrams RMC,
Simpson DM,
Navis A,
Jette N,
Zhou L,
Shin SC.
Small fiber neuropathy associated with SARS-CoV-2 infection. Muscle Nerve 2022; 65 (04) 440-443
50
Koyun D.
Neurological complication caused by zika virus: Guillain-Barré syndrome. Int J Biomed Clin Anal 2022; 2 (01) 20-28
51
Kazmi SS,
Ali W,
Bibi N,
Nouroz F.
A review on Zika virus outbreak, epidemiology, transmission and infection dynamics. J Biol Res (Thessalon) 2020; 27: 5
52
Carod-Artal FJ.
Neurological complications of Zika virus infection. Expert Rev Anti Infect Ther 2018; 16 (05) 399-410
53
Tyler KL,
Roos KL.
The expanding spectrum of Zika virus infections of the nervous system. JAMA Neurol 2017; 74 (10) 1169-1171
54
Adi-Dako O,
Kwapong AA,
Adukpo S.
Zika Virus Disease: Rising Contagious Diseases. Hoboken, NJ:
55
Bhandari R,
Gupta R,
Vashishth A,
Kuhad A.
Transient receptor potential vanilloid 1 (TRPV1) as a plausible novel therapeutic target for treating neurological complications in ZikaVirus. Med Hypotheses 2021; 156: 110685
56
Punsoni M,
Lakis NS,
Mellion M,
de la Monte SM.
Post-polio syndrome revisited. Neurol Int 2023; 15 (02) 569-579
57
Louis ED,
Mayer SA.
Merritt's Neurology. Philadelphia, PA: Lippincott Williams & Wilkins; 2021
58
Wasserstrom R,
Mamourian AC,
McGary CT,
Miller G.
Bulbar poliomyelitis: MR findings with pathologic correlation. AJNR Am J Neuroradiol 1992; 13 (01) 371-373
59
Russo GB,
Goyal T,
Tyler K,
Thakur KT.
Re-emergence of poliovirus in the United States: considerations and implications. Ann Neurol 2022; 92 (05) 725-728
60
Bai F,
Thompson EA,
Vig PJS,
Leis AA.
Current understanding of West Nile virus clinical manifestations, immune responses, neuroinvasion, and immunotherapeutic implications. Pathogens 2019; 8 (04) 193
61
Gray TJ,
Webb CE.
A review of the epidemiological and clinical aspects of West Nile virus. Int J Gen Med 2014; 7: 193-203
62
Boegle AK,
Narayanaswami P.
Infectious neuropathies. Continuum (Minneap Minn) 2023; 29 (05) 1418-1443
63
Hiraldo JDG,
Fuerte-Hortigón A,
Domínguez-Mayoral A.
et al.
Uncovering the neurological effects of West Nile virus during a record-breaking southern Spain outbreak in 2020-2021. J Neuroimmunol 2023; 383: 578179
64
Gilrane VL,
Zhuge J,
Huang W.
et al.
Biennial upsurge and molecular epidemiology of enterovirus D68 infection in New York, USA, 2014 to 2018. J Clin Microbiol 2020; 58 (09) e00284-20
65
Kidd S,
Lopez AS,
Konopka-Anstadt JL,
Nix WA,
Routh JA,
Oberste MS.
Enterovirus D68–associated acute flaccid myelitis, United States, 2020. Emerg Infect Dis 2020; 26 (10) e201630
66
Wang C,
Li J,
Liu Y,
Sun Q,
Liu Z.
Pathogenesis of enterovirus infection in central nervous system. Biosaf Health 2023; 5 (04) 233-239
67
Sooksawasdi Na Ayudhya S,
Laksono BM,
van Riel D.
The pathogenesis and virulence of enterovirus-D68 infection. Virulence 2021; 12 (01) 2060-2072
68
Musharrafieh R,
Zhang J,
Tuohy P.
et al.
Discovery of quinoline analogues as potent antivirals against enterovirus D68 (EV-D68). J Med Chem 2019; 62 (08) 4074-4090
69
Ulferts R,
de Boer SM,
van der Linden L.
et al.
Screening of a library of FDA-approved drugs identifies several enterovirus replication inhibitors that target viral protein 2C. Antimicrob Agents Chemother 2016; 60 (05) 2627-2638
70
Cardenas-de la Garza JA,
De la Cruz-Valadez E,
Ocampo-Candiani J,
Welsh O.
Clinical spectrum of Lyme disease. Eur J Clin Microbiol Infect Dis 2019; 38 (02) 201-208
71
Hansen K,
Crone C,
Kristoferitsch W.
Lyme neuroborreliosis. Handb Clin Neurol 2013; 115: 559-575
72
Halperin JJ.
Facial nerve palsy associated with lyme disease. Muscle Nerve 2003; 28 (04) 516-517
73
Wan L,
Yan A,
Reese E,
Thomas J,
Kissinger M.
Through the eyes of uncertainty: giant cell arteritis and Lyme neuroborreliosis in a story of vision loss. Cureus 2024; 16 (02) e53623
74
Omotosho YB,
Sherchan R,
Ying GW,
Shayuk M.
A unique case of bannwarth syndrome in early disseminated Lyme disease. Cureus 2021; 13 (04) e14680
75
Novak P,
Felsenstein D,
Mao C,
Octavien NR,
Zubcevik N.
Association of small fiber neuropathy and post treatment Lyme disease syndrome. PLoS One 2019; 14 (02) e0212222
76
Roos KL.
Neurologic complications of Lyme disease. Continuum (Minneap Minn) 2021; 27 (04) 1040-1050
77
Scollard D,
Stryjewska B,
Dacso M.
Leprosy: Epidemiology, Microbiology, Clinical Manifestations, and Diagnosis. Waltham, MA: UpToDate; 2020
78
Ebenezer GJ,
Scollard DM.
Treatment and evaluation advances in leprosy neuropathy. Neurotherapeutics 2021; 18 (04) 2337-2350
79
van Brakel WH,
Khawas IB.
Silent neuropathy in leprosy: an epidemiological description. Lepr Rev 1994; 65 (04) 350-360
80
Gupta OP,
Jain AP,
Jajoo UN,
Kumar K,
Parvez K.
Respiratory dysautonomia in leprosy. Indian J Lepr 1984; 56 (04) 844-846
81
Khadilkar SV,
Patil SB,
Shetty VP.
Neuropathies of leprosy. J Neurol Sci 2021; 420: 117288
82
Rao PN,
Suneetha S.
Pure neuritic leprosy: current status and relevance. Indian J Dermatol Venereol Leprol 2016; 82 (03) 252-261
83
Tsuboi M,
Evans J,
Davies EP.
et al.
Prevalence of syphilis among men who have sex with men: a global systematic review and meta-analysis from 2000-20. Lancet Glob Health 2021; 9 (08) e1110-e1118
84
Chaudhry S,
Akinlusi I,
Shi T,
Cervantes J.
Secondary syphilis: pathophysiology, clinical manifestations, and diagnostic testing. Venereology 2023; 2 (02) 65-75
85
Berger JR,
Dean D.
Neurosyphilis. Handb Clin Neurol 2014; 121: 1461-1472
86
Klein TA,
Ridley MB.
An old flame reignites: vagal neuropathy secondary to neurosyphilis. J Voice 2014; 28 (02) 255-257
87
Zhou J,
Zhang H,
Tang K,
Liu R,
Li J.
An updated review of recent advances in neurosyphilis. Front Med (Lausanne) 2022; 9: 800383
88
Kayabaşı M,
Köksaldı S,
Saatci AO,
Bajin MS.
Presentation of ocular syphilis with bilateral optic neuropathy. Neuroophthalmology 2023; 47 (5–6): 274-280
89
Clarke KEN,
MacNeil A,
Hadler S,
Scott C,
Tiwari TSP,
Cherian T.
Global epidemiology of diphtheria, 2000–2017(1). Emerg Infect Dis 2019; 25 (10) 1834-1842
90
Lozhnikova SM,
Pirogov VN,
Piradov MA,
Sakharova AV,
Liudkovskaia IG.
Diphtheritic polyneuropathy: clinico-morphologic study [in Russian]. Arkh Patol 1997; 59 (02) 11-17
91
Joshua AM,
Misri Z.
Peripheral nerve disorders. In: Physiotherapy for Adult Neurological Conditions. New York, NY: Springer; 2022: 621-729
92
Kobaidze K,
Wiley Z.
Botulism in the 21st Century: a scoping review. . Brown Hospital Medicine 2023;2(02)
93
Zhang J-C,
Sun L,
Nie Q-H.
Botulism, where are we now?. Clin Toxicol (Phila) 2010; 48 (09) 867-879
94
Hehir II MK,
Logigian EL.
Infectious neuropathies. Continuum (Minneap Minn) 2014; 20 (5 Peripheral Nervous System Disorders): 1274-1292
95
Howard Jr JF.
Electrodiagnosis of disorders of neuromuscular transmission. Phys Med Rehabil Clin N Am 2013; 24 (01) 169-192
96
Zivković SA,
Shipe C.
Use of repetitive nerve stimulation in the evaluation of neuromuscular junction disorders. Am J Electroneurodiagn Technol 2005; 45 (04) 248-261
97
Echeverría LE,
Marcus R,
Novick G.
et al.
WHF IASC roadmap on Chagas disease. Glob Heart 2020; 15 (01) 26
98
Robinson-Papp J.
Infectious neuropathies. Continuum (Minneap Minn) 2012; 18 (01) 126-138
99
Sica RE,
Gonzalez Cappa SM,
Sanz OP,
Mirkin G.
Peripheral nervous system involvement in human and experimental chronic American trypanosomiasis. Bull Soc Pathol Exot 1995; 88 (04) 156-163
100
WHO Expert Committee.
Control of Chagas disease. World Health Organ Tech Rep Ser 2002; 905: i-vi , 1–109, back cover
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