HIV-related Neuropathy: Difference between revisions

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<div class="editorbox"> '''Original Editor '''- [[User:Melissa Coetsee|Melissa Coetsee]] <br>
<div class="editorbox"> '''Original Editor '''- [[User:Melissa Coetsee|Melissa Coetsee]] <br>


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== Introduction ==
== Introduction ==
Despite the introduction of combination [[Antiretrovirals and HIV|antiretroviral therapy]] (ART), neuropathies (especially distal sensory neuropathy) are still a common complication of [[Human Immunodeficiency Virus (HIV)|HIV.]] It is associated with significant morbidity and negatively impacts quality of life.<ref name=":1">Schütz SG, Robinson-Papp J. H[https://www.tandfonline.com/doi/full/10.2147/HIV.S36674 IV-related neuropathy: current perspectives.] HIV/AIDS-Research and Palliative Care. 2013 Sep 11:243-51.</ref><ref>Biraguma J, Rhoda A. P[https://www.tandfonline.com/doi/full/10.1080/17290376.2012.683582 eripheral neuropathy and quality of life of adults living with HIV/AIDS in the Rulindo district of Rwanda.] SAHARA-J: Journal of Social Aspects of HIV/AIDS. 2012;9(2):88-94.</ref>
Despite the introduction of combination [[Antiretrovirals and HIV|antiretroviral therapy]] (ART), [[neuropathies]] are still a common complication of [[Human Immunodeficiency Virus (HIV)|HIV.]] The most common type of neuropathy found in PLWH (distal sensory polyneuropathy) is the leading cause of [[Chronic Pain|chronic pain]] in PLWH and is associated with significant morbidity and negatively impacts [[Quality of Life|quality of life.]]<ref name=":1">Schütz SG, Robinson-Papp J. H[https://www.tandfonline.com/doi/full/10.2147/HIV.S36674 IV-related neuropathy: current perspectives.] HIV/AIDS-Research and Palliative Care. 2013 Sep 11:243-51.</ref><ref>Biraguma J, Rhoda A. P[https://www.tandfonline.com/doi/full/10.1080/17290376.2012.683582 eripheral neuropathy and quality of life of adults living with HIV/AIDS in the Rulindo district of Rwanda.] SAHARA-J: Journal of Social Aspects of HIV/AIDS. 2012;9(2):88-94.</ref><ref name=":5">Amaniti A, Sardeli C, Fyntanidou V, Papakonstantinou P, Dalakakis I, Mylonas A, Sapalidis K, Kosmidis C, Katsaounis A, Giannakidis D, Koulouris C. [https://www.researchgate.net/publication/337618807_Pharmacologic_and_Non-Pharmacologic_Interventions_for_HIV-Neuropathy_Pain_A_Systematic_Review_and_a_Meta-Analysis#fullTextFileContent Pharmacologic and non-pharmacologic interventions for HIV-neuropathy pain. A systematic review and a meta-analysis.] Medicina. 2019 Nov 28;55(12):762.</ref>


== Epidemiology ==
== Epidemiology ==
The prevalence of HIV-associated neuropathy varies from 1.73% tot 69.4% among people living with HIV (PLWH).<ref>Yakasai AM, Maharaj S, Danazumi MS. Strength exercise for balance and gait in HIV-associated distal symmetrical polyneuropathy: A randomised controlled trial. Southern African Journal of HIV Medicine. 2021;22(1).</ref> This variability could be attributed to the introduction of ART, with its benefits and varying adverse effects with evolving drug-combinations. Diagnostic criteria and geographical region also influence the he prevalence of HIV-associated neuropathy.<ref name=":0">Howlett WP. [https://www.bioline.org.br/pdf?hs19079 Neurological disorders in HIV in Africa: a review.] African health sciences. 2019 Aug 20;19(2):1953-77.</ref> The estimated pooled frequency of DSN in Africa, prior to ART, was 27%. This increased to 52% in the post-ART era, and was mainly attributed to the widespread use of Nucleoside reverse transcriptase inhibitors (NRTIs) - like Stavudine.<ref name=":0" />
The prevalence of HIV-associated neuropathy varies from 1.73% tot 69.4% among people living with HIV (PLWH).<ref>Yakasai AM, Maharaj S, Danazumi MS. Strength exercise for balance and gait in HIV-associated distal symmetrical polyneuropathy: A randomised controlled trial. Southern African Journal of HIV Medicine. 2021;22(1).</ref> This variability could be attributed to the introduction of [[Antiretrovirals and HIV|antiretroviral treatment]] (ART), with its benefits and varying adverse effects with evolving drug-combinations. Diagnostic criteria and geographical region also influence the prevalence of HIV-associated neuropathy.<ref name=":0">Howlett WP. [https://www.bioline.org.br/pdf?hs19079 Neurological disorders in HIV in Africa: a review.] African health sciences. 2019 Aug 20;19(2):1953-77.</ref> The estimated pooled frequency of distal sensory polyneuropathy (DSPN) in Africa, prior to ART, was 27%. This increased to 52% in the post-ART era, and was mainly attributed to the widespread use of Nucleoside reverse transcriptase inhibitors (NRTIs) - like Stavudine.<ref name=":0" />


It is however important to note that although the frequency appears to have increased since the introduction of ART, some studies indicate a significant reduction in pain associated with neuropathy - i.e. although patients test positive for neuropathy (based on signs), it is often asymptomatic.<ref name=":0" />
It is however important to note that although the frequency appears to have increased since the introduction of ART, some studies indicate a significant reduction in pain associated with neuropathy - i.e. although patients test positive for neuropathy (based on signs), it is often asymptomatic.<ref name=":0" />
== Pathophysiology ==
== Pathophysiology ==
[[File:Nerve conduction.jpg|thumb|Peripheral nerve anatomy]]
[[File:Nerve conduction.jpg|thumb|Peripheral nerve anatomy|400x400px]]
Although other mechanisms may be at play for the less common types of neuropathy (discussed below), HIV-related neuropathy is usually as a result of '''two distinct pathological processes''' that lead to ''distal axonal degeneration, neuronal loss in the dorsal root ganglia and reduced epidermal nerve fibre density''<ref name=":1" />:
Although other mechanisms may be at play for the less common types of neuropathy (discussed below), HIV-related neuropathy is usually as a result of '''two distinct pathological processes''' that lead to ''distal axonal degeneration, neuronal loss in the dorsal root ganglia and reduced epidermal nerve fibre density''<ref name=":1" />:


# '''Neurotoxic effect of HIV:''' Indirect neurotoxicity as a result of viral proteins and an inflammatory response to HIV<ref name=":1" />  
# '''Neurotoxic effect of HIV:''' Indirect neurotoxicity as a result of viral proteins and an inflammatory response to HIV<ref name=":1" />  
# '''Neurotoxic effects of ART:''' Some ART drugs (NRTIs) associated with an increased incidence of peripheral neuropathy. These include Didanosine, Zalcitabine, Stavudine.<ref>Hogan C, Wilkins E. Neurological complications in HIV. Clinical Medicine.2011 Dec;11(6):571.</ref>ART related neuropathy typically develops 5-6 months after initiating ART.<ref name=":0" />
# '''Neurotoxic effects of ART:''' Some ART drugs (NRTIs) associated with an increased incidence of peripheral neuropathy. These include Didanosine, Zalcitabine, Stavudine.<ref>Hogan C, Wilkins E. Neurological complications in HIV. Clinical Medicine.2011 Dec;11(6):571.</ref>Mitochondrial dysfunction is the likely mechanism responsible for this.<ref name=":8">Winias S, Radithia D, Savitri Ernawati D. [[Neuropathy complication of antiretroviral therapy in HIV/AIDS patients.]] Oral Diseases. 2020 Sep;26:149-52.</ref> ART related neuropathy typically develops 5-6 months after initiating ART.<ref name=":0" />


Despite these two distinct pathological processes, the signs and symptoms of each process are not clinically distinguishable.<ref name=":1" />  
Despite these two distinct pathological processes, the signs and symptoms of each process are not clinically distinguishable.<ref name=":1" />  
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== Diagnostic Procedures  ==
== Diagnostic Procedures  ==


Diagnosis is based on medical history and clinical examination. This may included a confirmed HIV infection and NRTI exposure history, along with signs and symptoms related to neuropathy.
Diagnosis is based on medical history and clinical examination. A confirmed diagnosis of HIV infection is required, as well as a history regarding NRTI exposure. Signs and symptoms indicative of neuropathy need to be present, with specific patterns and findings guiding the differential diagnosis. If upper motor neuron signs are present (eg. increased tendon reflexes) other conditions need to be considered.


Additional tests (mostly to rule out other conditions) may include:
Additional tests (mostly to rule out other conditions) may include:


* '''Laboratory tests''' - CD4 count and viral load; Vit B levels; Diabetic screening
* '''Laboratory tests''' - CD4 count and viral load; vitamin B levels; diabetic screening
* '''[[Nerve Conduction Study|Nerve conduction studies]]''' - not routinely indicated<ref name=":1" />
* '''[[Nerve Conduction Study|Nerve conduction studies]]''' - Not routinely indicated<ref name=":1" />
* '''[[Quantitative Sensory Testing (QST)|Quantitative Sensory Testing]]''' - will reveal abnormalities in cases of peripheral and central nerve disorders
* '''[[Quantitative Sensory Testing (QST)|Quantitative Sensory Testing]]''' - Will reveal abnormalities in cases of peripheral and central nerve disorders


For '''Distal Sensory Polyneuropathy''' (DSPN), a clinical diagnostic tool called HIV-associated Neuropathy Tool (CHANT) has been validated for use in Africa, and include the following assessment areas:<ref>Woldeamanuel YW, Kamerman PR, Veliotes DG, Phillips TJ, Asboe D, Boffito M, Rice AS. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072607/ Development, validation, and field-testing of an instrument for clinical assessment of HIV-associated neuropathy and neuropathic pain in resource-restricted and large population study settings.] PLoS One. 2016 Oct 20;11(10):e0164994.</ref>
For '''Distal Sensory Polyneuropathy''' (DSPN), a clinical diagnostic tool called HIV-associated Neuropathy Tool (CHANT) has been validated for use in Africa, and include the following assessment areas:<ref>Woldeamanuel YW, Kamerman PR, Veliotes DG, Phillips TJ, Asboe D, Boffito M, Rice AS. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072607/ Development, validation, and field-testing of an instrument for clinical assessment of HIV-associated neuropathy and neuropathic pain in resource-restricted and large population study settings.] PLoS One. 2016 Oct 20;11(10):e0164994.</ref>
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* Bilateral feet pain
* Bilateral feet pain
* Bilateral feet numbness
* Bilateral feet numbness
* Bilateral ankle reflex - diminished
* Bilateral ankle reflex - Diminished
* Bilateral big toe vibration detection - diminished
* Bilateral big toe vibration detection - Diminished
** The following minimum combinations are required to diagnose a patient with PNS: Bilateral feet pain/ reduced great toe vibrations '''AND''' Bilateral feet numbness/ reduced ankle reflex
** The following minimum combinations are required to diagnose a patient with PNS: Bilateral feet pain/ reduced great toe vibrations '''AND''' Bilateral feet numbness/ reduced ankle reflex


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Also see [[Neurological Complications of HIV]] and [[Neuropathies]]
Also see [[Neurological Complications of HIV]] and [[Neuropathies]]


* [[Myelopathy]] - including Vacuolar Myelopathy and [[Pott's Disease]]
* [[Myelopathy]] - Including Vacuolar Myelopathy and [[Pott's Disease]]
* Opportunistic infections affecting the CNS - TB Meningitis, Neurosyphilis, Toxoplasmosis [[Encephalitis]], Cryptococcal [[Meningitis]]
* Opportunistic infections affecting the CNS - TB Meningitis, Neurosyphilis, Toxoplasmosis [[Encephalitis]], Cryptococcal [[Meningitis]]
* Other CNS conditions - [[Stroke]], [[Lymphoma]], Aseptic Meningitis
* Other CNS conditions - [[Stroke]], [[Lymphoma]], Aseptic Meningitis
* [[Vitamin B12 Deficiency|Vitamin B deficiency]] - Vit B12 deficient or excess of vit B6
* [[Vitamin B12 Deficiency|Vitamin B deficiency]] - Especially vitamin B12 and B6
* Alcoholic neuropathy
* Alcoholic neuropathy
* [[Diabetic Neuropathy]]
* [[Diabetic Neuropathy]]
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=== B-Vitamins and HIV ===
=== B-Vitamins and HIV ===
B-vitamin deficiencies are prevalent in PLWH and are associated with poor health outcomes. HIV itself causes vitamin-B deficiencies through various mechanisms mostly related to poor absorption.<ref name=":2">Layden AJ, Finkelstein JL. [https://www.ncbi.nlm.nih.gov/books/NBK572219/ B-vitamins and HIV/AIDS. Nutrition and HIV: Epidemiological Evidence to Public Health.] 2018 May 15:27-87.</ref>Since vitamin-B6 and B12 play have important immune support functions (eg. synthesis of CD4 cells), sufficient amounts of these vitamins could play a protective role HIV progression.<ref name=":2" /> Insufficient vitamin B levels could increase the risk of HIV-related neuropathy as Vitamin B12 is also involved in myelin production.  
B-vitamin deficiencies are prevalent in PLWH and are associated with poor health outcomes. HIV itself causes vitamin-B deficiencies through various mechanisms mostly related to poor absorption.<ref name=":2">Layden AJ, Finkelstein JL. [https://www.ncbi.nlm.nih.gov/books/NBK572219/ B-vitamins and HIV/AIDS. Nutrition and HIV: Epidemiological Evidence to Public Health.] 2018 May 15:27-87.</ref>Since vitamin-B6 and B12 have important immune support functions (eg. synthesis of CD4 cells), sufficient amounts of these vitamins could play a protective role in HIV progression.<ref name=":2" /> Insufficient vitamin B levels could increase the risk of HIV-related neuropathy as Vitamin B12 is also involved in myelin production
 
Isoniazid, a drug used in the treatment of [[Tuberculosis]] (TB), can also cause a vitamin B6 deficiency. Since TB is prevalent among PLWH in Africa, this is another mechanisms that could affect vitamin B levels.  


== Outcome Measures  ==
== Outcome Measures  ==
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== Types of Neuropathy ==
== Types of Neuropathy ==
Neuropathy can occur at all stage of HIV, and various types of neuropathy have been documented. The neuropathies present in PLWH include<ref name=":0" />:
Neuropathy can occur at all stages of HIV, and various types of neuropathies have been documented. The neuropathies present in PLWH include<ref name=":0" />:


# '''Distal sensory polyneuropathy (DSPN)'''
# '''Distal sensory polyneuropathy (DSPN)'''
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=== 1. Distal Sensory Polyneuropathy (DSPN) ===
=== 1. Distal Sensory Polyneuropathy (DSPN) ===
DSPN is the most common type of neuropathy in PLWH.<ref name=":0" />It affects the distal extremities (more commonly the feet, symmetric) and is caused by axonal damage secondary to dorsal root inflammation. It is more common in the advanced stages of HIV infection (WHO stages 3 and 4). Some patients with DSPN (about 25%) do not experiences any sensory symptoms (asymptomatic DSPN).<ref name=":0" />  
[[File:Sensory Neuropathy.jpg|thumb|Image indicating the distribution of sensory neuropathy in HIV]]
DSPN is the most common type of neuropathy in PLWH.<ref name=":0" />It affects the distal extremities (more commonly the feet, symmetrically) and is caused by axonal damage secondary to dorsal root inflammation. Some patients with DSPN (about 25%) do not experiences any sensory symptoms (asymptomatic DSPN), but for most PLWH it is associated with neuropathic pain .<ref name=":0" /><ref name=":5" />  


'''Signs and symptoms''' include<ref name=":0" /><ref name=":1" />:
'''Signs and symptoms''' include<ref name=":0" /><ref name=":1" />:


* Burning, stabbing pain and numbness in the soles of the feet/palms of the hands - this ascends symmetrically (stocking-glove distribution)
* Distal symmetric sensory symptoms: burning, stabbing pain and numbness in the soles of the feet/palms of the hands - this ascends symmetrically (stocking-glove distribution)
* Sensitivity is most pronounced one the soles and palms
* [[Allodynia]] and Hyperalgesia: sensitivity is most pronounced one the soles and palms
* Reduced or absent ankle reflexes
* Reduced or absent ankle [[reflexes]]
* Impaired pin prick and vibration sensation
* Impaired pin prick and vibration sensation
* Impaired proprioception of the affected region
* Impaired [[proprioception]] of the affected region
* Weakness and atrophy are rare as only sensory nerves are involved
* Weakness and atrophy are rare as only sensory nerves are involved


'''Risk factors''' for developing DSN<ref name=":0" /><ref name=":1" />:
'''Risk factors''' for developing DSPN<ref name=":0" /><ref name=":1" />:


* Advanced immunosuppression
* Advanced immunosuppression


* Lower CD4 count and high viral load
* Lower CD4 count and high viral load
* A history of prior TB or alcohol abuse
* A history of prior [[Tuberculosis|TB]] or alcohol abuse
* ART regime that includes Dideoxynucleoside revers transcriptase inhibitors (NRTIs), especially Stavudine
* ART regime that includes Dideoxynucleoside revers transcriptase inhibitors (NRTIs), especially Stavudine
* Height and ethnicity may play a role<ref name=":1" />
* Height and ethnicity may play a role<ref name=":1" />
* Diabetes may exacerbate the risk of neuropathy in PLWH<ref name=":1" />
* [[Diabetes]] may exacerbate the risk of neuropathy in PLWH<ref name=":1" />
* Psychosocial factors
* Psychosocial factors: [[depression]] seems to be associated with greater pain intensity<ref name=":5" />


=== 2. Inflammatory Neuropathies ===
=== 2. Inflammatory Neuropathies ===
Although uncommon, two forms of autoimmune inflammatory demyelinating polyneuropathy (IDP) can occur in PLWH<ref name=":1" />:
Although uncommon, two forms of autoimmune inflammatory demyelinating polyneuropathy (IDP) can occur in PLWH<ref name=":1" />:


# '''Acute IDP''' [[Guillain-Barre Syndrome|(Guillan-Barré syndrome)]] - rapidly progressive symptoms, with symmetrical limb weakness and areflexia. Can occur with intact immunity or at seroconversion.<ref name=":0" />
# '''Acute IDP''' [[Guillain-Barre Syndrome|(Guillan-Barré syndrome)]] - Rapidly progressive symptoms, with symmetrical limb weakness and areflexia. Can occur with intact immunity or at seroconversion.<ref name=":0" />
# '''Chronic IDP''' - slower progression, often with a relapsing-remitting pattern; symmetrical limb weakness with areflexia and sensory symptoms. Usually associated with moderately advanced HIV disease.<ref name=":0" />
# '''Chronic IDP''' - Slower progression, often with a relapsing-remitting pattern; symmetrical limb weakness with areflexia and sensory symptoms. Usually associated with moderately advanced HIV disease.<ref name=":0" />


Both forms are characterised by ascending muscle weakness and areflexia with paraesthesia<ref name=":1" />
Both forms are characterised by ascending muscle weakness and areflexia with paraesthesia<ref name=":1" />


=== 3. Radiculopathy ===
=== 3. Radiculopathy ===
Radiculopathy in less common and when present usually affects the lumbosacral nerve roots, mostly caused by [[Tuberculosis]], Cytomegalovirus (CMV) or [[lymphoma]].<ref name=":1" /><ref name=":0" />This results in flaccid paraplegia with areflexia and urinary incontinence without upper limb involvement.<ref name=":0" />  
Radiculopathy in less common and when present usually affects the lumbosacral nerve roots, mostly caused by [[Tuberculosis]], Cytomegalovirus (CMV) or [[lymphoma]].<ref name=":1" /><ref name=":0" />This results in flaccid paraplegia with areflexia and [[Urinary Incontinence|urinary incontinence]] without upper limb involvement.<ref name=":0" />  


=== 4. Mononeuropathy ===
=== 4. Mononeuropathy ===
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== Medical Management  ==
== Medical Management  ==


* '''HIV infection control -''' early diagnosis and treatment with ART
* '''HIV infection control -''' Early diagnosis and treatment with ART
* '''Drug regime alteration if associated with ART -''' Avoiding NRTIs; discontinuing Stavudine if symptomatic DSP develops<ref name=":1" />  
* '''Drug regime alteration if associated with ART -''' Avoiding NRTIs; discontinuing Stavudine if symptomatic DSPN develops<ref name=":1" />  
* '''Pain control'''
* '''Pain control'''
** With ''neuropathic medication (''amitriptyline, gabapentin, pregabalin)<ref name=":0" />- Although these medications have proven effectiveness in other neuropathic conditions, they seem to be less effective in HIV-related neuropathy. Gabapentin appears to be superior to other medications.<ref name=":1" />
** ''Neuropathic medication'' (amitriptyline, gabapentin, pregabalin)<ref name=":0" />- Although these medications have proven effectiveness in other neuropathic conditions, they seem to be less effective in HIV-related neuropathy, with studies showing no superiority to placebo in PLWH.<ref name=":1" /><ref name=":8" />
** Topical ''capsaicin patches'' have shown promise in reducing neuropathic pain in PLWH<ref name=":1" />
** Topical ''capsaicin patches'' have shown promise in reducing neuropathic pain in PLWH.<ref name=":1" />
** Complete resolution of pain is not common, but reduction is possible<ref name=":1" />
** Complete resolution of pain is not common, but reduction is possible.<ref name=":1" />
** See the page on [[Neuropathic Pain]] and [[Pain in People Living with HIV|Pain in PLWH]]
** See the page on [[Neuropathic Pain]] and [[Pain in People Living with HIV|Pain in PLWH]]
* '''Education -''' On possible other causes of neuropathy (alcohol, diabetes and Vit B6 deficiency secondary to isoniazid)<ref name=":0" />
* '''Education -''' On possible other causes of neuropathy (alcohol, diabetes and vitamin B deficiency)<ref name=":0" />
* '''Optimisation of contributing factors''' - medical management of diabetes, alcohol abuse and vitamin deficiencies (especially vitamin B supplementation)<ref name=":1" /><ref name=":2" />
* '''Optimisation of contributing factors''' - Medical management of diabetes, alcohol abuse and vitamin deficiencies (especially vitamin B supplementation)<ref name=":1" /><ref name=":2" />
* '''Treatment of other infections/diroders -''' in the case of Herpes reactivation, treatment with acyclovir is indicated.<ref name=":0" />Autoimmune inflammatory neuropathies require immunomodulation (acute type) or steroid treatment (chronic type)<ref name=":0" />.  
* '''Treatment of other infections/disorders -''' in the case of Herpes reactivation, treatment with acyclovir is indicated.<ref name=":0" />Autoimmune inflammatory neuropathies require immunomodulation (acute type) or steroid treatment (chronic type)<ref name=":0" />.  


== Role of Physiotherapy ==
== Role of Physiotherapy ==


* '''Fall prevention:''' Even mild forms of neuropathy can result in altered [[gait]] and [[balance]] which increases the risk of [[Falls|falls.]]<ref name=":3" />Gait and balance training may reduce [[Falls Risk Assessment Tool (FRAT)|fall risk]] and [[assistive devices]] can be prescribed to ensure improved, safer mobilisation. See [[Falls and Exercise]]  
* '''Fall prevention:''' Even mild forms of neuropathy can result in altered [[gait]] and [[balance]] which increases the risk of [[Falls|falls.]]<ref name=":3">Yakasai AM, Maharaj S, Danazumi MS. S[[trength exercise for balance and gait in HIV-associated distal symmetrical polyneuropathy: A randomised controlled trial.]] Southern African Journal of HIV Medicine. 2021;22(1).</ref>Gait and balance training may reduce [[Falls Risk Assessment Tool (FRAT)|fall risk]] and [[assistive devices]] can be prescribed to ensure improved, safer mobilisation. See [[Falls and Exercise]]  
* '''Pain management:''' Neuropathies are often accompanied by neuropathic pain. A recent systematic review recommended exercise (resistance and aerobic) as an effective treatment to reduce neuropathic pain in PLWH<ref name=":4" />. See [[Neuropathic Pain]]
* '''Pain management:''' Neuropathies are often accompanied by [[Neuropathic Pain|neuropathic pain.]] A recent systematic review recommended exercise (resistance and aerobic) as a potentially effective treatment to reduce neuropathic pain in PLWH<ref name=":4">Zhang YH, Hu HY, Xiong YC, Peng C, Hu L, Kong YZ, Wang YL, Guo JB, Bi S, Li TS, Ao LJ. [https://www.researchgate.net/publication/356650979_Exercise_for_Neuropathic_Pain_A_Systematic_Review_and_Expert_Consensus Exercise for neuropathic pain: a systematic review and expert consensus.] Frontiers in Medicine. 2021 Nov 24;8:756940.</ref>. HIV-associated neuropathic pain does however appear to be more refractory to treatment than other neuropathic pain conditions<ref name=":8" />. See [[Neuropathic Pain]]
* '''Resistance and Aerobic Exercises:''' A recent systematic review concluded that there is sufficient evidence that progressive resistance training improves balance, gait, and quality of life in PLWH on ART. <ref name=":5" />See [[Exercise for People Living with HIV|Exercise for PLWH.]]
* '''Resistance and Aerobic Exercises:''' A recent systematic review concluded that there is sufficient evidence that progressive resistance training and [[Aerobic Exercise|aerobic exercise]] improves balance, gait, and quality of life in PLWH on ART. <ref name=":5" />See [[Exercise for People Living with HIV|Exercise for PLWH.]]
** Most of these studies focused on DSPN
** Most of the studies focused on DSPN
** Studies were conducted in a wide range of settings, including African settings (Rwanda and Zimbabwe).<ref name=":3" /><ref name=":6" /><ref name=":7" />
** Studies were conducted in a wide range of settings, including African settings (Rwanda and Zimbabwe).<ref name=":3" /><ref name=":6">Mkandla K, Myezwa H, Musenge E. The effects of progressive-resisted exercises on muscle strength and health-related quality of life in persons with HIV-related poly-neuropathy in Zimbabwe. AIDS care. 2016 May 3;28(5):639-43.</ref><ref name=":7">Stewart A, Tumusiime DK, Musenge E, Venter FW. [https://sajp.co.za/index.php/sajp/article/view/1328/1782 The effects of a physiotherapist-led exercise intervention on peripheral neuropathy among people living with HIV on antiretroviral therapy in Kigali, Rwanda.] South African Journal of Physiotherapy. 2019 Jan 1;75(1):1-9.</ref>
** Strengthening exercises should focus on lower limb muscle groups (quadriceps, tibialis anterior, hamstrings and gastrocnemius)<ref name=":6" />
** Strengthening exercises should focus on lower limb muscle groups (quadriceps, tibialis anterior, hamstrings and gastrocnemius).<ref name=":6" />
** Aerobic exercise should be of moderate intensity and can include brisk walking and cycling.
** Aerobic exercise should be of moderate intensity and can include brisk walking and cycling.
** The optimal duration of exercise programs appear to be 12 weeks, 2-3 times per week.<ref name=":5" />
** The optimal duration of exercise programs appear to be 12 weeks, 2-3 times per week.<ref name=":5" />
** Although exercise has many proven benefits on symptoms and function, it does not however seem to alter neuropathy signs in the short term (absent reflexes and vibration sense)<ref name=":7" /> - this seems to suggest that exercise works by modifying pain modulation and compensatory strategies, rather than altering pathology. It is still however unsure whether long term results may indicate different findings.
** Although exercise has many proven benefits on symptoms and function, it does not seem to alter neuropathy signs in the short term (absent reflexes and vibration sense)<ref name=":7" /> - this seems to suggest that exercise works by affecting pain modulation and compensatory strategies, rather than altering pathology. It is still however unsure whether long term results may indicate different findings.


* '''Neural mobility exercises:''' Sliding and tensioning techniques may enhance nerve gliding and improve [[Neurodynamic Treatment|neural mobility]]. This could translate into reduced pain and improved function by allowing more range of movement<ref name=":7" />.
* '''Neural mobility exercises:''' Sliding and tensioning techniques may enhance nerve gliding and improve [[Neurodynamic Treatment|neural mobility]]. This could translate into reduced pain and improved function by allowing more range of movement<ref name=":7" />.
* '''Psychosocial factors:''' Assessing and exploring psychosocial factors that contribute to pain and/or non-adherence to medication/interventions
* '''Psychosocial factors:''' Assessing and exploring psychosocial factors that contribute to pain and/or non-adherence to medication/interventions
* '''Foot care''': Education on proper footwear, hygiene and fall prevention; daily foot evaluation for skin damage
* '''Foot care''': Education on proper footwear, foot hygiene and fall prevention. Since sensation in the feet are altered, daily foot evaluation for skin damage is important.
 
== Resources ==
 
1 Yakasai <ref name=":3">Yakasai AM, Maharaj S, Danazumi MS. S[[trength exercise for balance and gait in HIV-associated distal symmetrical polyneuropathy: A randomised controlled trial.]] Southern African Journal of HIV Medicine. 2021;22(1).</ref>Mkandla <ref name=":6">Mkandla K, Myezwa H, Musenge E. The effects of progressive-resisted exercises on muscle strength and health-related quality of life in persons with HIV-related poly-neuropathy in Zimbabwe. AIDS care. 2016 May 3;28(5):639-43.</ref>Zhang <ref name=":4">Zhang YH, Hu HY, Xiong YC, Peng C, Hu L, Kong YZ, Wang YL, Guo JB, Bi S, Li TS, Ao LJ. [https://www.researchgate.net/publication/356650979_Exercise_for_Neuropathic_Pain_A_Systematic_Review_and_Expert_Consensus Exercise for neuropathic pain: a systematic review and expert consensus.] Frontiers in Medicine. 2021 Nov 24;8:756940.</ref>Winias<ref>Winias S, Radithia D, Savitri Ernawati D. [[Neuropathy complication of antiretroviral therapy in HIV/AIDS patients.]] Oral Diseases. 2020 Sep;26:149-52.</ref>Amaniti<ref name=":5">Amaniti A, Sardeli C, Fyntanidou V, Papakonstantinou P, Dalakakis I, Mylonas A, Sapalidis K, Kosmidis C, Katsaounis A, Giannakidis D, Koulouris C. [https://www.researchgate.net/publication/337618807_Pharmacologic_and_Non-Pharmacologic_Interventions_for_HIV-Neuropathy_Pain_A_Systematic_Review_and_a_Meta-Analysis#fullTextFileContent Pharmacologic and non-pharmacologic interventions for HIV-neuropathy pain. A systematic review and a meta-analysis.] Medicina. 2019 Nov 28;55(12):762.</ref>Tumusiime<ref name=":7">Stewart A, Tumusiime DK, Musenge E, Venter FW. [https://sajp.co.za/index.php/sajp/article/view/1328/1782 The effects of a physiotherapist-led exercise intervention on peripheral neuropathy among people living with HIV on antiretroviral therapy in Kigali, Rwanda.] South African Journal of Physiotherapy. 2019 Jan 1;75(1):1-9.</ref>
 
== References  ==
== References  ==


<references />
<references />

Revision as of 13:55, 12 December 2023

Original Editor - Melissa Coetsee
Top Contributors - Melissa Coetsee, Kim Jackson and Pacifique Dusabeyezu

Introduction[edit | edit source]

Despite the introduction of combination antiretroviral therapy (ART), neuropathies are still a common complication of HIV. The most common type of neuropathy found in PLWH (distal sensory polyneuropathy) is the leading cause of chronic pain in PLWH and is associated with significant morbidity and negatively impacts quality of life.[1][2][3]

Epidemiology[edit | edit source]

The prevalence of HIV-associated neuropathy varies from 1.73% tot 69.4% among people living with HIV (PLWH).[4] This variability could be attributed to the introduction of antiretroviral treatment (ART), with its benefits and varying adverse effects with evolving drug-combinations. Diagnostic criteria and geographical region also influence the prevalence of HIV-associated neuropathy.[5] The estimated pooled frequency of distal sensory polyneuropathy (DSPN) in Africa, prior to ART, was 27%. This increased to 52% in the post-ART era, and was mainly attributed to the widespread use of Nucleoside reverse transcriptase inhibitors (NRTIs) - like Stavudine.[5]

It is however important to note that although the frequency appears to have increased since the introduction of ART, some studies indicate a significant reduction in pain associated with neuropathy - i.e. although patients test positive for neuropathy (based on signs), it is often asymptomatic.[5]

Pathophysiology[edit | edit source]

Peripheral nerve anatomy

Although other mechanisms may be at play for the less common types of neuropathy (discussed below), HIV-related neuropathy is usually as a result of two distinct pathological processes that lead to distal axonal degeneration, neuronal loss in the dorsal root ganglia and reduced epidermal nerve fibre density[1]:

  1. Neurotoxic effect of HIV: Indirect neurotoxicity as a result of viral proteins and an inflammatory response to HIV[1]
  2. Neurotoxic effects of ART: Some ART drugs (NRTIs) associated with an increased incidence of peripheral neuropathy. These include Didanosine, Zalcitabine, Stavudine.[6]Mitochondrial dysfunction is the likely mechanism responsible for this.[7] ART related neuropathy typically develops 5-6 months after initiating ART.[5]

Despite these two distinct pathological processes, the signs and symptoms of each process are not clinically distinguishable.[1]

Clinical Presentation[edit | edit source]

Clinical presentation varies depending on the type of neuropathy (discussed below), but may include:

  • Numbness
  • Burning pain
  • Altered sensation, including numbness and/or hypersensitivity
  • Loss of balance as a result of impaired proprioception
  • Diminished or absent lower limb reflexes
  • Muscle weakness and muscle wasting (if motor nerves are affected)

Patients may present with functional limitations and chronic painful symptoms. When poorly managed, this can contribute to anxiety, depression and loss of independence.

Diagnostic Procedures[edit | edit source]

Diagnosis is based on medical history and clinical examination. A confirmed diagnosis of HIV infection is required, as well as a history regarding NRTI exposure. Signs and symptoms indicative of neuropathy need to be present, with specific patterns and findings guiding the differential diagnosis. If upper motor neuron signs are present (eg. increased tendon reflexes) other conditions need to be considered.

Additional tests (mostly to rule out other conditions) may include:

For Distal Sensory Polyneuropathy (DSPN), a clinical diagnostic tool called HIV-associated Neuropathy Tool (CHANT) has been validated for use in Africa, and include the following assessment areas:[8]

  • Bilateral feet pain
  • Bilateral feet numbness
  • Bilateral ankle reflex - Diminished
  • Bilateral big toe vibration detection - Diminished
    • The following minimum combinations are required to diagnose a patient with PNS: Bilateral feet pain/ reduced great toe vibrations AND Bilateral feet numbness/ reduced ankle reflex

Differential Diagnosis[edit | edit source]

Also see Neurological Complications of HIV and Neuropathies

B-Vitamins and HIV[edit | edit source]

B-vitamin deficiencies are prevalent in PLWH and are associated with poor health outcomes. HIV itself causes vitamin-B deficiencies through various mechanisms mostly related to poor absorption.[9]Since vitamin-B6 and B12 have important immune support functions (eg. synthesis of CD4 cells), sufficient amounts of these vitamins could play a protective role in HIV progression.[9] Insufficient vitamin B levels could increase the risk of HIV-related neuropathy as Vitamin B12 is also involved in myelin production.

Isoniazid, a drug used in the treatment of Tuberculosis (TB), can also cause a vitamin B6 deficiency. Since TB is prevalent among PLWH in Africa, this is another mechanisms that could affect vitamin B levels.

Outcome Measures[edit | edit source]

Types of Neuropathy[edit | edit source]

Neuropathy can occur at all stages of HIV, and various types of neuropathies have been documented. The neuropathies present in PLWH include[5]:

  1. Distal sensory polyneuropathy (DSPN)
  2. Inflammatory neuropathies
  3. Radiculopathies
  4. Mononeuropathies

1. Distal Sensory Polyneuropathy (DSPN)[edit | edit source]

Image indicating the distribution of sensory neuropathy in HIV

DSPN is the most common type of neuropathy in PLWH.[5]It affects the distal extremities (more commonly the feet, symmetrically) and is caused by axonal damage secondary to dorsal root inflammation. Some patients with DSPN (about 25%) do not experiences any sensory symptoms (asymptomatic DSPN), but for most PLWH it is associated with neuropathic pain .[5][3]

Signs and symptoms include[5][1]:

  • Distal symmetric sensory symptoms: burning, stabbing pain and numbness in the soles of the feet/palms of the hands - this ascends symmetrically (stocking-glove distribution)
  • Allodynia and Hyperalgesia: sensitivity is most pronounced one the soles and palms
  • Reduced or absent ankle reflexes
  • Impaired pin prick and vibration sensation
  • Impaired proprioception of the affected region
  • Weakness and atrophy are rare as only sensory nerves are involved

Risk factors for developing DSPN[5][1]:

  • Advanced immunosuppression
  • Lower CD4 count and high viral load
  • A history of prior TB or alcohol abuse
  • ART regime that includes Dideoxynucleoside revers transcriptase inhibitors (NRTIs), especially Stavudine
  • Height and ethnicity may play a role[1]
  • Diabetes may exacerbate the risk of neuropathy in PLWH[1]
  • Psychosocial factors: depression seems to be associated with greater pain intensity[3]

2. Inflammatory Neuropathies[edit | edit source]

Although uncommon, two forms of autoimmune inflammatory demyelinating polyneuropathy (IDP) can occur in PLWH[1]:

  1. Acute IDP (Guillan-Barré syndrome) - Rapidly progressive symptoms, with symmetrical limb weakness and areflexia. Can occur with intact immunity or at seroconversion.[5]
  2. Chronic IDP - Slower progression, often with a relapsing-remitting pattern; symmetrical limb weakness with areflexia and sensory symptoms. Usually associated with moderately advanced HIV disease.[5]

Both forms are characterised by ascending muscle weakness and areflexia with paraesthesia[1]

3. Radiculopathy[edit | edit source]

Radiculopathy in less common and when present usually affects the lumbosacral nerve roots, mostly caused by Tuberculosis, Cytomegalovirus (CMV) or lymphoma.[1][5]This results in flaccid paraplegia with areflexia and urinary incontinence without upper limb involvement.[5]

4. Mononeuropathy[edit | edit source]

PLWH are at increased risk of mononeuropathies. The most common mononeuropathies are[5]:

  • Facial nerve palsy (Bell's palsy): Usually occurs during the early, asymptomatic stages of HIV (at seroconversion). It may present as part of an acute inflammatory demyelinating neuropathy, but this is less common.
  • Herpes zoster reactivation: One of the earliest signs of HIV, and affects the thoracic and trigeminal nerve. Complications include myelitis and post herpetic neuralgia.
  • Median neuropathy: Leading to carpal tunnel syndrome

Medical Management[edit | edit source]

  • HIV infection control - Early diagnosis and treatment with ART
  • Drug regime alteration if associated with ART - Avoiding NRTIs; discontinuing Stavudine if symptomatic DSPN develops[1]
  • Pain control
    • Neuropathic medication (amitriptyline, gabapentin, pregabalin)[5]- Although these medications have proven effectiveness in other neuropathic conditions, they seem to be less effective in HIV-related neuropathy, with studies showing no superiority to placebo in PLWH.[1][7]
    • Topical capsaicin patches have shown promise in reducing neuropathic pain in PLWH.[1]
    • Complete resolution of pain is not common, but reduction is possible.[1]
    • See the page on Neuropathic Pain and Pain in PLWH
  • Education - On possible other causes of neuropathy (alcohol, diabetes and vitamin B deficiency)[5]
  • Optimisation of contributing factors - Medical management of diabetes, alcohol abuse and vitamin deficiencies (especially vitamin B supplementation)[1][9]
  • Treatment of other infections/disorders - in the case of Herpes reactivation, treatment with acyclovir is indicated.[5]Autoimmune inflammatory neuropathies require immunomodulation (acute type) or steroid treatment (chronic type)[5].

Role of Physiotherapy[edit | edit source]

  • Fall prevention: Even mild forms of neuropathy can result in altered gait and balance which increases the risk of falls.[10]Gait and balance training may reduce fall risk and assistive devices can be prescribed to ensure improved, safer mobilisation. See Falls and Exercise
  • Pain management: Neuropathies are often accompanied by neuropathic pain. A recent systematic review recommended exercise (resistance and aerobic) as a potentially effective treatment to reduce neuropathic pain in PLWH[11]. HIV-associated neuropathic pain does however appear to be more refractory to treatment than other neuropathic pain conditions[7]. See Neuropathic Pain
  • Resistance and Aerobic Exercises: A recent systematic review concluded that there is sufficient evidence that progressive resistance training and aerobic exercise improves balance, gait, and quality of life in PLWH on ART. [3]See Exercise for PLWH.
    • Most of the studies focused on DSPN
    • Studies were conducted in a wide range of settings, including African settings (Rwanda and Zimbabwe).[10][12][13]
    • Strengthening exercises should focus on lower limb muscle groups (quadriceps, tibialis anterior, hamstrings and gastrocnemius).[12]
    • Aerobic exercise should be of moderate intensity and can include brisk walking and cycling.
    • The optimal duration of exercise programs appear to be 12 weeks, 2-3 times per week.[3]
    • Although exercise has many proven benefits on symptoms and function, it does not seem to alter neuropathy signs in the short term (absent reflexes and vibration sense)[13] - this seems to suggest that exercise works by affecting pain modulation and compensatory strategies, rather than altering pathology. It is still however unsure whether long term results may indicate different findings.
  • Neural mobility exercises: Sliding and tensioning techniques may enhance nerve gliding and improve neural mobility. This could translate into reduced pain and improved function by allowing more range of movement[13].
  • Psychosocial factors: Assessing and exploring psychosocial factors that contribute to pain and/or non-adherence to medication/interventions
  • Foot care: Education on proper footwear, foot hygiene and fall prevention. Since sensation in the feet are altered, daily foot evaluation for skin damage is important.

References[edit | edit source]

  1. 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 1.14 1.15 1.16 Schütz SG, Robinson-Papp J. HIV-related neuropathy: current perspectives. HIV/AIDS-Research and Palliative Care. 2013 Sep 11:243-51.
  2. Biraguma J, Rhoda A. Peripheral neuropathy and quality of life of adults living with HIV/AIDS in the Rulindo district of Rwanda. SAHARA-J: Journal of Social Aspects of HIV/AIDS. 2012;9(2):88-94.
  3. 3.0 3.1 3.2 3.3 3.4 Amaniti A, Sardeli C, Fyntanidou V, Papakonstantinou P, Dalakakis I, Mylonas A, Sapalidis K, Kosmidis C, Katsaounis A, Giannakidis D, Koulouris C. Pharmacologic and non-pharmacologic interventions for HIV-neuropathy pain. A systematic review and a meta-analysis. Medicina. 2019 Nov 28;55(12):762.
  4. Yakasai AM, Maharaj S, Danazumi MS. Strength exercise for balance and gait in HIV-associated distal symmetrical polyneuropathy: A randomised controlled trial. Southern African Journal of HIV Medicine. 2021;22(1).
  5. 5.00 5.01 5.02 5.03 5.04 5.05 5.06 5.07 5.08 5.09 5.10 5.11 5.12 5.13 5.14 5.15 5.16 5.17 Howlett WP. Neurological disorders in HIV in Africa: a review. African health sciences. 2019 Aug 20;19(2):1953-77.
  6. Hogan C, Wilkins E. Neurological complications in HIV. Clinical Medicine.2011 Dec;11(6):571.
  7. 7.0 7.1 7.2 Winias S, Radithia D, Savitri Ernawati D. Neuropathy complication of antiretroviral therapy in HIV/AIDS patients. Oral Diseases. 2020 Sep;26:149-52.
  8. Woldeamanuel YW, Kamerman PR, Veliotes DG, Phillips TJ, Asboe D, Boffito M, Rice AS. Development, validation, and field-testing of an instrument for clinical assessment of HIV-associated neuropathy and neuropathic pain in resource-restricted and large population study settings. PLoS One. 2016 Oct 20;11(10):e0164994.
  9. 9.0 9.1 9.2 Layden AJ, Finkelstein JL. B-vitamins and HIV/AIDS. Nutrition and HIV: Epidemiological Evidence to Public Health. 2018 May 15:27-87.
  10. 10.0 10.1 Yakasai AM, Maharaj S, Danazumi MS. Strength exercise for balance and gait in HIV-associated distal symmetrical polyneuropathy: A randomised controlled trial. Southern African Journal of HIV Medicine. 2021;22(1).
  11. Zhang YH, Hu HY, Xiong YC, Peng C, Hu L, Kong YZ, Wang YL, Guo JB, Bi S, Li TS, Ao LJ. Exercise for neuropathic pain: a systematic review and expert consensus. Frontiers in Medicine. 2021 Nov 24;8:756940.
  12. 12.0 12.1 Mkandla K, Myezwa H, Musenge E. The effects of progressive-resisted exercises on muscle strength and health-related quality of life in persons with HIV-related poly-neuropathy in Zimbabwe. AIDS care. 2016 May 3;28(5):639-43.
  13. 13.0 13.1 13.2 Stewart A, Tumusiime DK, Musenge E, Venter FW. The effects of a physiotherapist-led exercise intervention on peripheral neuropathy among people living with HIV on antiretroviral therapy in Kigali, Rwanda. South African Journal of Physiotherapy. 2019 Jan 1;75(1):1-9.