Increases in CSF dopamine in HIV patients are due to the dopamine transporter 10/10-repeat allele which is more frequent in HIV-infected individuals

Dysfunction of dopaminergic neurotransmission has been implicated in HIV infection. We showed previously increased dopamine (DA) levels in CSF of therapy-naïve HIV patients and an inverse correlation between CSF DA and CD4 counts in the periphery, suggesting adverse effects of high levels of DA on H...

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Veröffentlicht in:Journal of Neural Transmission 2013-10, Vol.120 (10), p.1411-1419
Hauptverfasser: Horn, Anne, Scheller, Carsten, du Plessis, Stefan, Arendt, Gabriele, Nolting, Thorsten, Joska, John, Sopper, Sieghart, Maschke, Matthias, Obermann, Mark, Husstedt, Ingo W., Hain, Johannes, Maponga, Tongai, Riederer, Peter, Koutsilieri, Eleni
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container_issue 10
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container_title Journal of Neural Transmission
container_volume 120
creator Horn, Anne
Scheller, Carsten
du Plessis, Stefan
Arendt, Gabriele
Nolting, Thorsten
Joska, John
Sopper, Sieghart
Maschke, Matthias
Obermann, Mark
Husstedt, Ingo W.
Hain, Johannes
Maponga, Tongai
Riederer, Peter
Koutsilieri, Eleni
description Dysfunction of dopaminergic neurotransmission has been implicated in HIV infection. We showed previously increased dopamine (DA) levels in CSF of therapy-naïve HIV patients and an inverse correlation between CSF DA and CD4 counts in the periphery, suggesting adverse effects of high levels of DA on HIV infection. In the current study including a total of 167 HIV-positive and negative donors from Germany and South Africa (SA), we investigated the mechanistic background for the increase of CSF DA in HIV individuals. Interestingly, we found that the DAT 10/10-repeat allele is present more frequently within HIV individuals than in uninfected subjects. Logistic regression analysis adjusted for gender and ethnicity showed an odds ratio for HIV infection in DAT 10/10 allele carriers of 3.93 (95 % CI 1.72–8.96; p  = 0.001, Fishers exact test). 42.6 % HIV-infected patients harbored the DAT 10/10 allele compared to only 10.5 % uninfected DAT 10/10 carriers in SA (odds ratio 6.31), whereas 68.1 versus 40.9 %, respectively, in Germany (odds ratio 3.08). Subjects homozygous for the 10-repeat allele had higher amounts of CSF DA and reduced DAT mRNA expression but similar disease severity compared with those carrying other DAT genotypes. These intriguing and novel findings show the mutual interaction between DA and HIV, suggesting caution in the interpretation of CNS DA alterations in HIV infection solely as a secondary phenomenon to the virus and open the door for larger studies investigating consequences of the DAT functional polymorphism on HIV epidemiology and progression of disease.
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We showed previously increased dopamine (DA) levels in CSF of therapy-naïve HIV patients and an inverse correlation between CSF DA and CD4 counts in the periphery, suggesting adverse effects of high levels of DA on HIV infection. In the current study including a total of 167 HIV-positive and negative donors from Germany and South Africa (SA), we investigated the mechanistic background for the increase of CSF DA in HIV individuals. Interestingly, we found that the DAT 10/10-repeat allele is present more frequently within HIV individuals than in uninfected subjects. Logistic regression analysis adjusted for gender and ethnicity showed an odds ratio for HIV infection in DAT 10/10 allele carriers of 3.93 (95 % CI 1.72–8.96; p  = 0.001, Fishers exact test). 42.6 % HIV-infected patients harbored the DAT 10/10 allele compared to only 10.5 % uninfected DAT 10/10 carriers in SA (odds ratio 6.31), whereas 68.1 versus 40.9 %, respectively, in Germany (odds ratio 3.08). Subjects homozygous for the 10-repeat allele had higher amounts of CSF DA and reduced DAT mRNA expression but similar disease severity compared with those carrying other DAT genotypes. 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Subjects homozygous for the 10-repeat allele had higher amounts of CSF DA and reduced DAT mRNA expression but similar disease severity compared with those carrying other DAT genotypes. These intriguing and novel findings show the mutual interaction between DA and HIV, suggesting caution in the interpretation of CNS DA alterations in HIV infection solely as a secondary phenomenon to the virus and open the door for larger studies investigating consequences of the DAT functional polymorphism on HIV epidemiology and progression of disease.</abstract><cop>Vienna</cop><pub>Springer Vienna</pub><pmid>24057505</pmid><doi>10.1007/s00702-013-1086-x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
AIDS Dementia Complex - cerebrospinal fluid
AIDS Dementia Complex - genetics
Alleles
CD4 antigen
Dopamine - cerebrospinal fluid
Dopamine Plasma Membrane Transport Proteins - genetics
Female
Genotype
HIV Infections - cerebrospinal fluid
HIV Infections - genetics
Human immunodeficiency virus
Humans
Male
Medicine
Medicine & Public Health
Middle Aged
Neurology
Neurosciences
Odds Ratio
Polymorphism, Genetic
Psychiatry
Reverse Transcriptase Polymerase Chain Reaction
Translational Neurosciences - Original
Translational Neurosciences - Original Article
Young Adult
title Increases in CSF dopamine in HIV patients are due to the dopamine transporter 10/10-repeat allele which is more frequent in HIV-infected individuals
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