Cerebral FDG-PET scanning abnormalities in optimally treated HIV patients

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Cerebral FDG-PET scanning abnormalities in optimally treated HIV patients. / Andersen, Ase B; Law, Ian; Krabbe, Karen S; Bruunsgaard, Helle; Ostrowski, Sisse R; Ullum, Henrik; Højgaard, Liselotte; Lebech, Annemette; Gerstoft, Jan; Kjaer, Andreas.

In: Journal of Neuroinflammation, Vol. 7, 14.02.2010, p. 13.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Andersen, AB, Law, I, Krabbe, KS, Bruunsgaard, H, Ostrowski, SR, Ullum, H, Højgaard, L, Lebech, A, Gerstoft, J & Kjaer, A 2010, 'Cerebral FDG-PET scanning abnormalities in optimally treated HIV patients', Journal of Neuroinflammation, vol. 7, pp. 13. https://doi.org/10.1186/1742-2094-7-13

APA

Andersen, A. B., Law, I., Krabbe, K. S., Bruunsgaard, H., Ostrowski, S. R., Ullum, H., Højgaard, L., Lebech, A., Gerstoft, J., & Kjaer, A. (2010). Cerebral FDG-PET scanning abnormalities in optimally treated HIV patients. Journal of Neuroinflammation, 7, 13. https://doi.org/10.1186/1742-2094-7-13

Vancouver

Andersen AB, Law I, Krabbe KS, Bruunsgaard H, Ostrowski SR, Ullum H et al. Cerebral FDG-PET scanning abnormalities in optimally treated HIV patients. Journal of Neuroinflammation. 2010 Feb 14;7:13. https://doi.org/10.1186/1742-2094-7-13

Author

Andersen, Ase B ; Law, Ian ; Krabbe, Karen S ; Bruunsgaard, Helle ; Ostrowski, Sisse R ; Ullum, Henrik ; Højgaard, Liselotte ; Lebech, Annemette ; Gerstoft, Jan ; Kjaer, Andreas. / Cerebral FDG-PET scanning abnormalities in optimally treated HIV patients. In: Journal of Neuroinflammation. 2010 ; Vol. 7. pp. 13.

Bibtex

@article{e7694376e1e24f7cae9e3ae7bbd4bba4,
title = "Cerebral FDG-PET scanning abnormalities in optimally treated HIV patients",
abstract = "BACKGROUND: The long-term neurological consequences of HIV infection and treatment are not yet completely understood. In this study we examined the prevalence of cerebral metabolic abnormalities among a cohort of neurologically intact HIV patients with fully suppressed HIV viral loads. Concomitant analyses of circulating brain derived neurotrophic factor (BDNF) were performed to correlate these abnormalities with potential signs of neuro-regenerating/protective activity, and concomitant analyses of circulating tumour necrosis factor (TNF) alpha, interleukin (IL) 6, and soluble urokinase plasminogen activator receptor (suPAR) were performed to correlate these abnormalities with potential signs of neurodegenerative processes.METHODS: The study population consisted of HIV-positive patients known to be infected for more than 5 years and on antiretroviral (ARV) treatment for a minimum of three years with no history of virological failure, a CD4 count above 200 x 106 cells/l and no other co-morbidities. The distribution of the regional cerebral metabolic rate of glucose metabolism was measured using fluorine-18-flourodeoxyglucose positron emission tomography (FDG-PET) scanning. The PET scans were evaluated for individual pathology using Neurostat software and for group pathology using statistical parametric mapping (SPM). Circulating levels of BDNF, TNF alpha, IL-6 and suPAR were measured by ELISA techniques.RESULTS: More than half (55%) of the patients exhibited varying severities of mesial frontal reduction in the relative metabolic rate of glucose. Compared to healthy subjects, the patients with abnormal FDG-PET scanning results had a shorter history of known HIV infection, fewer years on antiretroviral therapy and higher levels of circulating TNF alpha and IL-6 (p = 0.08).CONCLUSION: A large proportion of optimally treated HIV patients exhibit cerebral FDG-PET scanning abnormalities and elevated TNF alpha and IL-6 levels, which may indicate imminent neuronal damage. The neuroprotective effect of early ARV treatment should be considered in future prospective follow-up studies.",
keywords = "Adult, Aged, Brain Mapping, Cerebral Cortex, Cytokines, Female, Fluorodeoxyglucose F18, HIV Infections, Humans, Male, Middle Aged, Positron-Emission Tomography, Journal Article, Research Support, Non-U.S. Gov't",
author = "Andersen, {Ase B} and Ian Law and Krabbe, {Karen S} and Helle Bruunsgaard and Ostrowski, {Sisse R} and Henrik Ullum and Liselotte H{\o}jgaard and Annemette Lebech and Jan Gerstoft and Andreas Kjaer",
year = "2010",
month = feb,
day = "14",
doi = "10.1186/1742-2094-7-13",
language = "English",
volume = "7",
pages = "13",
journal = "Journal of Neuroinflammation",
issn = "1742-2094",
publisher = "BioMed Central",

}

RIS

TY - JOUR

T1 - Cerebral FDG-PET scanning abnormalities in optimally treated HIV patients

AU - Andersen, Ase B

AU - Law, Ian

AU - Krabbe, Karen S

AU - Bruunsgaard, Helle

AU - Ostrowski, Sisse R

AU - Ullum, Henrik

AU - Højgaard, Liselotte

AU - Lebech, Annemette

AU - Gerstoft, Jan

AU - Kjaer, Andreas

PY - 2010/2/14

Y1 - 2010/2/14

N2 - BACKGROUND: The long-term neurological consequences of HIV infection and treatment are not yet completely understood. In this study we examined the prevalence of cerebral metabolic abnormalities among a cohort of neurologically intact HIV patients with fully suppressed HIV viral loads. Concomitant analyses of circulating brain derived neurotrophic factor (BDNF) were performed to correlate these abnormalities with potential signs of neuro-regenerating/protective activity, and concomitant analyses of circulating tumour necrosis factor (TNF) alpha, interleukin (IL) 6, and soluble urokinase plasminogen activator receptor (suPAR) were performed to correlate these abnormalities with potential signs of neurodegenerative processes.METHODS: The study population consisted of HIV-positive patients known to be infected for more than 5 years and on antiretroviral (ARV) treatment for a minimum of three years with no history of virological failure, a CD4 count above 200 x 106 cells/l and no other co-morbidities. The distribution of the regional cerebral metabolic rate of glucose metabolism was measured using fluorine-18-flourodeoxyglucose positron emission tomography (FDG-PET) scanning. The PET scans were evaluated for individual pathology using Neurostat software and for group pathology using statistical parametric mapping (SPM). Circulating levels of BDNF, TNF alpha, IL-6 and suPAR were measured by ELISA techniques.RESULTS: More than half (55%) of the patients exhibited varying severities of mesial frontal reduction in the relative metabolic rate of glucose. Compared to healthy subjects, the patients with abnormal FDG-PET scanning results had a shorter history of known HIV infection, fewer years on antiretroviral therapy and higher levels of circulating TNF alpha and IL-6 (p = 0.08).CONCLUSION: A large proportion of optimally treated HIV patients exhibit cerebral FDG-PET scanning abnormalities and elevated TNF alpha and IL-6 levels, which may indicate imminent neuronal damage. The neuroprotective effect of early ARV treatment should be considered in future prospective follow-up studies.

AB - BACKGROUND: The long-term neurological consequences of HIV infection and treatment are not yet completely understood. In this study we examined the prevalence of cerebral metabolic abnormalities among a cohort of neurologically intact HIV patients with fully suppressed HIV viral loads. Concomitant analyses of circulating brain derived neurotrophic factor (BDNF) were performed to correlate these abnormalities with potential signs of neuro-regenerating/protective activity, and concomitant analyses of circulating tumour necrosis factor (TNF) alpha, interleukin (IL) 6, and soluble urokinase plasminogen activator receptor (suPAR) were performed to correlate these abnormalities with potential signs of neurodegenerative processes.METHODS: The study population consisted of HIV-positive patients known to be infected for more than 5 years and on antiretroviral (ARV) treatment for a minimum of three years with no history of virological failure, a CD4 count above 200 x 106 cells/l and no other co-morbidities. The distribution of the regional cerebral metabolic rate of glucose metabolism was measured using fluorine-18-flourodeoxyglucose positron emission tomography (FDG-PET) scanning. The PET scans were evaluated for individual pathology using Neurostat software and for group pathology using statistical parametric mapping (SPM). Circulating levels of BDNF, TNF alpha, IL-6 and suPAR were measured by ELISA techniques.RESULTS: More than half (55%) of the patients exhibited varying severities of mesial frontal reduction in the relative metabolic rate of glucose. Compared to healthy subjects, the patients with abnormal FDG-PET scanning results had a shorter history of known HIV infection, fewer years on antiretroviral therapy and higher levels of circulating TNF alpha and IL-6 (p = 0.08).CONCLUSION: A large proportion of optimally treated HIV patients exhibit cerebral FDG-PET scanning abnormalities and elevated TNF alpha and IL-6 levels, which may indicate imminent neuronal damage. The neuroprotective effect of early ARV treatment should be considered in future prospective follow-up studies.

KW - Adult

KW - Aged

KW - Brain Mapping

KW - Cerebral Cortex

KW - Cytokines

KW - Female

KW - Fluorodeoxyglucose F18

KW - HIV Infections

KW - Humans

KW - Male

KW - Middle Aged

KW - Positron-Emission Tomography

KW - Journal Article

KW - Research Support, Non-U.S. Gov't

U2 - 10.1186/1742-2094-7-13

DO - 10.1186/1742-2094-7-13

M3 - Journal article

C2 - 20152054

VL - 7

SP - 13

JO - Journal of Neuroinflammation

JF - Journal of Neuroinflammation

SN - 1742-2094

ER -

ID: 180570840