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Higher CSF Ferritin Heavy-Chain (Fth1) and Transferrin Predict Better Neurocognitive Performance in People with HIV
HIV-associated neurocognitive disorder (HAND) remains prevalent despite antiretroviral therapy and involves white matter damage in the brain. Although iron is essential for myelination and myelin maintenance/repair, its role in HAND is largely unexplored. We tested the hypotheses that cerebrospinal...
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Published in: | Molecular neurobiology 2021-10, Vol.58 (10), p.4842-4855 |
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creator | Kaur, Harpreet Bush, William S. Letendre, Scott L. Ellis, Ronald J. Heaton, Robert K. Patton, Stephanie M. Connor, James R. Samuels, David C. Franklin, Donald R. Hulgan, Todd Kallianpur, Asha R. |
description | HIV-associated neurocognitive disorder (HAND) remains prevalent despite antiretroviral therapy and involves white matter damage in the brain. Although iron is essential for myelination and myelin maintenance/repair, its role in HAND is largely unexplored. We tested the hypotheses that cerebrospinal fluid (CSF) heavy-chain ferritin (Fth1) and transferrin, proteins integral to iron delivery and myelination, are associated with neurocognitive performance in people with HIV (PWH). Fth1, transferrin, and the pro-inflammatory cytokines TNF-α and IL-6 were quantified in CSF at baseline (entry) in 403 PWH from a prospective observational study who underwent serial, comprehensive neurocognitive assessments. Associations of Fth1 and transferrin with Global Deficit Score (GDS)-defined neurocognitive performance at baseline and 30–42 months of follow-up were evaluated by multivariable regression. While not associated with neurocognitive performance at baseline, higher baseline CSF Fth1 predicted significantly better neurocognitive performance over 30 months in all PWH (
p <
0.05), in PWH aged < 50 at 30, 36, and 42 months (all
p
< 0.05), and in virally suppressed PWH at all three visit time-points (all
p
< 0.01). Higher CSF transferrin was associated with superior neurocognitive performance at all visits, primarily in viremic individuals (all
p
< 0.05). All associations persisted after adjustment for neuro-inflammation. In summary, higher CSF Fth1 is neuroprotective over prolonged follow-up in all and virally suppressed PWH, while higher CSF transferrin may be most neuroprotective during viremia. We speculate that higher CSF levels of these critical iron-delivery proteins support improved myelination and consequently, neurocognitive performance in PWH, providing a rationale for investigating their role in interventions to prevent and/or treat HAND. |
doi_str_mv | 10.1007/s12035-021-02433-7 |
format | article |
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p <
0.05), in PWH aged < 50 at 30, 36, and 42 months (all
p
< 0.05), and in virally suppressed PWH at all three visit time-points (all
p
< 0.01). Higher CSF transferrin was associated with superior neurocognitive performance at all visits, primarily in viremic individuals (all
p
< 0.05). All associations persisted after adjustment for neuro-inflammation. In summary, higher CSF Fth1 is neuroprotective over prolonged follow-up in all and virally suppressed PWH, while higher CSF transferrin may be most neuroprotective during viremia. We speculate that higher CSF levels of these critical iron-delivery proteins support improved myelination and consequently, neurocognitive performance in PWH, providing a rationale for investigating their role in interventions to prevent and/or treat HAND.</description><identifier>ISSN: 0893-7648</identifier><identifier>EISSN: 1559-1182</identifier><identifier>DOI: 10.1007/s12035-021-02433-7</identifier><identifier>PMID: 34195939</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adult ; AIDS Dementia Complex - cerebrospinal fluid ; AIDS Dementia Complex - diagnosis ; AIDS Dementia Complex - psychology ; Alzheimer's disease ; Antiretroviral drugs ; Antiretroviral therapy ; Bioavailability ; Biomarkers - cerebrospinal fluid ; Biomedical and Life Sciences ; Biomedicine ; Brain injury ; Brain research ; Cell Biology ; Cerebrospinal fluid ; Charters ; Cognition ; Comorbidity ; Drug therapy ; Female ; Ferritin ; Ferritins - cerebrospinal fluid ; HIV ; HIV Infections - cerebrospinal fluid ; HIV Infections - diagnosis ; HIV Infections - psychology ; Homeostasis ; Human immunodeficiency virus ; Humans ; Hypotheses ; Infections ; Inflammation ; Interleukin 6 ; Iron ; Longitudinal Studies ; Male ; Medicine ; Mental Status and Dementia Tests ; Metabolism ; Middle Aged ; Myelination ; Neurobiology ; Neurology ; Neuroprotection ; Neurosciences ; Oxidoreductases - cerebrospinal fluid ; Predictive Value of Tests ; Prospective Studies ; Proteins ; Psychiatry ; Substantia alba ; Transferrin - cerebrospinal fluid ; Transferrins ; Tumor necrosis factor-α ; Viremia</subject><ispartof>Molecular neurobiology, 2021-10, Vol.58 (10), p.4842-4855</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021</rights><rights>2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-a3966ec2da8e1d2f7f3a8d9fc82ce0551e16fdf395f0a164cf7119b45988a1df3</citedby><cites>FETCH-LOGICAL-c474t-a3966ec2da8e1d2f7f3a8d9fc82ce0551e16fdf395f0a164cf7119b45988a1df3</cites><orcidid>0000-0002-6483-523X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34195939$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaur, Harpreet</creatorcontrib><creatorcontrib>Bush, William S.</creatorcontrib><creatorcontrib>Letendre, Scott L.</creatorcontrib><creatorcontrib>Ellis, Ronald J.</creatorcontrib><creatorcontrib>Heaton, Robert K.</creatorcontrib><creatorcontrib>Patton, Stephanie M.</creatorcontrib><creatorcontrib>Connor, James R.</creatorcontrib><creatorcontrib>Samuels, David C.</creatorcontrib><creatorcontrib>Franklin, Donald R.</creatorcontrib><creatorcontrib>Hulgan, Todd</creatorcontrib><creatorcontrib>Kallianpur, Asha R.</creatorcontrib><title>Higher CSF Ferritin Heavy-Chain (Fth1) and Transferrin Predict Better Neurocognitive Performance in People with HIV</title><title>Molecular neurobiology</title><addtitle>Mol Neurobiol</addtitle><addtitle>Mol Neurobiol</addtitle><description>HIV-associated neurocognitive disorder (HAND) remains prevalent despite antiretroviral therapy and involves white matter damage in the brain. Although iron is essential for myelination and myelin maintenance/repair, its role in HAND is largely unexplored. We tested the hypotheses that cerebrospinal fluid (CSF) heavy-chain ferritin (Fth1) and transferrin, proteins integral to iron delivery and myelination, are associated with neurocognitive performance in people with HIV (PWH). Fth1, transferrin, and the pro-inflammatory cytokines TNF-α and IL-6 were quantified in CSF at baseline (entry) in 403 PWH from a prospective observational study who underwent serial, comprehensive neurocognitive assessments. Associations of Fth1 and transferrin with Global Deficit Score (GDS)-defined neurocognitive performance at baseline and 30–42 months of follow-up were evaluated by multivariable regression. While not associated with neurocognitive performance at baseline, higher baseline CSF Fth1 predicted significantly better neurocognitive performance over 30 months in all PWH (
p <
0.05), in PWH aged < 50 at 30, 36, and 42 months (all
p
< 0.05), and in virally suppressed PWH at all three visit time-points (all
p
< 0.01). Higher CSF transferrin was associated with superior neurocognitive performance at all visits, primarily in viremic individuals (all
p
< 0.05). All associations persisted after adjustment for neuro-inflammation. In summary, higher CSF Fth1 is neuroprotective over prolonged follow-up in all and virally suppressed PWH, while higher CSF transferrin may be most neuroprotective during viremia. We speculate that higher CSF levels of these critical iron-delivery proteins support improved myelination and consequently, neurocognitive performance in PWH, providing a rationale for investigating their role in interventions to prevent and/or treat HAND.</description><subject>Adult</subject><subject>AIDS Dementia Complex - cerebrospinal fluid</subject><subject>AIDS Dementia Complex - diagnosis</subject><subject>AIDS Dementia Complex - psychology</subject><subject>Alzheimer's disease</subject><subject>Antiretroviral drugs</subject><subject>Antiretroviral therapy</subject><subject>Bioavailability</subject><subject>Biomarkers - cerebrospinal fluid</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain injury</subject><subject>Brain research</subject><subject>Cell Biology</subject><subject>Cerebrospinal fluid</subject><subject>Charters</subject><subject>Cognition</subject><subject>Comorbidity</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Ferritin</subject><subject>Ferritins - cerebrospinal fluid</subject><subject>HIV</subject><subject>HIV Infections - cerebrospinal fluid</subject><subject>HIV Infections - diagnosis</subject><subject>HIV Infections - psychology</subject><subject>Homeostasis</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Infections</subject><subject>Inflammation</subject><subject>Interleukin 6</subject><subject>Iron</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medicine</subject><subject>Mental Status and Dementia Tests</subject><subject>Metabolism</subject><subject>Middle Aged</subject><subject>Myelination</subject><subject>Neurobiology</subject><subject>Neurology</subject><subject>Neuroprotection</subject><subject>Neurosciences</subject><subject>Oxidoreductases - cerebrospinal fluid</subject><subject>Predictive Value of Tests</subject><subject>Prospective Studies</subject><subject>Proteins</subject><subject>Psychiatry</subject><subject>Substantia alba</subject><subject>Transferrin - 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cerebrospinal fluid</topic><topic>AIDS Dementia Complex - diagnosis</topic><topic>AIDS Dementia Complex - psychology</topic><topic>Alzheimer's disease</topic><topic>Antiretroviral drugs</topic><topic>Antiretroviral therapy</topic><topic>Bioavailability</topic><topic>Biomarkers - cerebrospinal fluid</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain injury</topic><topic>Brain research</topic><topic>Cell Biology</topic><topic>Cerebrospinal fluid</topic><topic>Charters</topic><topic>Cognition</topic><topic>Comorbidity</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Ferritin</topic><topic>Ferritins - cerebrospinal fluid</topic><topic>HIV</topic><topic>HIV Infections - cerebrospinal fluid</topic><topic>HIV Infections - diagnosis</topic><topic>HIV Infections - psychology</topic><topic>Homeostasis</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Infections</topic><topic>Inflammation</topic><topic>Interleukin 6</topic><topic>Iron</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Medicine</topic><topic>Mental Status and Dementia Tests</topic><topic>Metabolism</topic><topic>Middle Aged</topic><topic>Myelination</topic><topic>Neurobiology</topic><topic>Neurology</topic><topic>Neuroprotection</topic><topic>Neurosciences</topic><topic>Oxidoreductases - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular neurobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaur, Harpreet</au><au>Bush, William S.</au><au>Letendre, Scott L.</au><au>Ellis, Ronald J.</au><au>Heaton, Robert K.</au><au>Patton, Stephanie M.</au><au>Connor, James R.</au><au>Samuels, David C.</au><au>Franklin, Donald R.</au><au>Hulgan, Todd</au><au>Kallianpur, Asha R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Higher CSF Ferritin Heavy-Chain (Fth1) and Transferrin Predict Better Neurocognitive Performance in People with HIV</atitle><jtitle>Molecular neurobiology</jtitle><stitle>Mol Neurobiol</stitle><addtitle>Mol Neurobiol</addtitle><date>2021-10-01</date><risdate>2021</risdate><volume>58</volume><issue>10</issue><spage>4842</spage><epage>4855</epage><pages>4842-4855</pages><issn>0893-7648</issn><eissn>1559-1182</eissn><abstract>HIV-associated neurocognitive disorder (HAND) remains prevalent despite antiretroviral therapy and involves white matter damage in the brain. Although iron is essential for myelination and myelin maintenance/repair, its role in HAND is largely unexplored. We tested the hypotheses that cerebrospinal fluid (CSF) heavy-chain ferritin (Fth1) and transferrin, proteins integral to iron delivery and myelination, are associated with neurocognitive performance in people with HIV (PWH). Fth1, transferrin, and the pro-inflammatory cytokines TNF-α and IL-6 were quantified in CSF at baseline (entry) in 403 PWH from a prospective observational study who underwent serial, comprehensive neurocognitive assessments. Associations of Fth1 and transferrin with Global Deficit Score (GDS)-defined neurocognitive performance at baseline and 30–42 months of follow-up were evaluated by multivariable regression. While not associated with neurocognitive performance at baseline, higher baseline CSF Fth1 predicted significantly better neurocognitive performance over 30 months in all PWH (
p <
0.05), in PWH aged < 50 at 30, 36, and 42 months (all
p
< 0.05), and in virally suppressed PWH at all three visit time-points (all
p
< 0.01). Higher CSF transferrin was associated with superior neurocognitive performance at all visits, primarily in viremic individuals (all
p
< 0.05). All associations persisted after adjustment for neuro-inflammation. In summary, higher CSF Fth1 is neuroprotective over prolonged follow-up in all and virally suppressed PWH, while higher CSF transferrin may be most neuroprotective during viremia. We speculate that higher CSF levels of these critical iron-delivery proteins support improved myelination and consequently, neurocognitive performance in PWH, providing a rationale for investigating their role in interventions to prevent and/or treat HAND.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>34195939</pmid><doi>10.1007/s12035-021-02433-7</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-6483-523X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult AIDS Dementia Complex - cerebrospinal fluid AIDS Dementia Complex - diagnosis AIDS Dementia Complex - psychology Alzheimer's disease Antiretroviral drugs Antiretroviral therapy Bioavailability Biomarkers - cerebrospinal fluid Biomedical and Life Sciences Biomedicine Brain injury Brain research Cell Biology Cerebrospinal fluid Charters Cognition Comorbidity Drug therapy Female Ferritin Ferritins - cerebrospinal fluid HIV HIV Infections - cerebrospinal fluid HIV Infections - diagnosis HIV Infections - psychology Homeostasis Human immunodeficiency virus Humans Hypotheses Infections Inflammation Interleukin 6 Iron Longitudinal Studies Male Medicine Mental Status and Dementia Tests Metabolism Middle Aged Myelination Neurobiology Neurology Neuroprotection Neurosciences Oxidoreductases - cerebrospinal fluid Predictive Value of Tests Prospective Studies Proteins Psychiatry Substantia alba Transferrin - cerebrospinal fluid Transferrins Tumor necrosis factor-α Viremia |
title | Higher CSF Ferritin Heavy-Chain (Fth1) and Transferrin Predict Better Neurocognitive Performance in People with HIV |
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