Minimally invasive biomarker confirms glial activation present in Alzheimer's disease: a preliminary study
Napapon Sailasuta, Kent Harris, Thao Tran, Brian RossClinical MR Unit, Huntington Medical Research Institutes, Pasadena, CA, USAAbstract: We applied 13C magnetic resonance spectroscopy (MRS), a nonradioactive, noninvasive brain imaging technique, to quantify the oxidation of [1-13C] acetate in a con...
Guardado en:
Autores principales: | , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Dove Medical Press
2011
|
Materias: | |
Acceso en línea: | https://doaj.org/article/5ba6dcdf4ac942c3afd7e47b352ab4ae |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:5ba6dcdf4ac942c3afd7e47b352ab4ae |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:5ba6dcdf4ac942c3afd7e47b352ab4ae2021-12-02T03:27:57ZMinimally invasive biomarker confirms glial activation present in Alzheimer's disease: a preliminary study1176-63281178-2021https://doaj.org/article/5ba6dcdf4ac942c3afd7e47b352ab4ae2011-08-01T00:00:00Zhttp://www.dovepress.com/minimally-invasive-biomarker-confirms-glial-activation-present-in-alzh-a8143https://doaj.org/toc/1176-6328https://doaj.org/toc/1178-2021Napapon Sailasuta, Kent Harris, Thao Tran, Brian RossClinical MR Unit, Huntington Medical Research Institutes, Pasadena, CA, USAAbstract: We applied 13C magnetic resonance spectroscopy (MRS), a nonradioactive, noninvasive brain imaging technique, to quantify the oxidation of [1-13C] acetate in a conventional clinical magnetic resonance imaging (MRI) scanner in five consecutive elderly subjects at various clinical stages of Alzheimer's disease (AD) progression. [1-13C] acetate entered the brain and was metabolized to [5-13C] glutamate and glutamine, as well as [1-13C] glutamate and glutamine, and the final glial oxidation product, 13C bicarbonate, at a linear rate. Calculation of the initial slope was similar in a single subject, examined twice, 1 month apart (test-re-test 8%). Mean rate of cerebral bicarbonate production in this elderly group was 0.040 ± 0.01 (n = 5). Assuming that the rate of conversion of acetate to bicarbonate is a reflection of glial metabolic rate and that glial metabolic rate is a surrogate marker for 'neuroinflammation', our preliminary results suggest that [1-13C] MRS may provide biomarkers for diseases, believed to involve microglia and other cells of the astrocyte series. Among these is AD, for which novel drugs which ameliorate the damaging effects of neuroinflammation before symptoms of dementia appear, are in advanced development. The value of 13C MRS as an early, noninvasive biomarker may lie in the conduct of cost-effective clinical trials.Keywords: Alzheimer's disease, noninvasive biomarker, glial activationTran THarris KSailasuta NRoss BDove Medical PressarticleNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571Neurology. Diseases of the nervous systemRC346-429ENNeuropsychiatric Disease and Treatment, Vol 2011, Iss Issue 1, Pp 495-499 (2011) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Neurosciences. Biological psychiatry. Neuropsychiatry RC321-571 Neurology. Diseases of the nervous system RC346-429 |
spellingShingle |
Neurosciences. Biological psychiatry. Neuropsychiatry RC321-571 Neurology. Diseases of the nervous system RC346-429 Tran T Harris K Sailasuta N Ross B Minimally invasive biomarker confirms glial activation present in Alzheimer's disease: a preliminary study |
description |
Napapon Sailasuta, Kent Harris, Thao Tran, Brian RossClinical MR Unit, Huntington Medical Research Institutes, Pasadena, CA, USAAbstract: We applied 13C magnetic resonance spectroscopy (MRS), a nonradioactive, noninvasive brain imaging technique, to quantify the oxidation of [1-13C] acetate in a conventional clinical magnetic resonance imaging (MRI) scanner in five consecutive elderly subjects at various clinical stages of Alzheimer's disease (AD) progression. [1-13C] acetate entered the brain and was metabolized to [5-13C] glutamate and glutamine, as well as [1-13C] glutamate and glutamine, and the final glial oxidation product, 13C bicarbonate, at a linear rate. Calculation of the initial slope was similar in a single subject, examined twice, 1 month apart (test-re-test 8%). Mean rate of cerebral bicarbonate production in this elderly group was 0.040 ± 0.01 (n = 5). Assuming that the rate of conversion of acetate to bicarbonate is a reflection of glial metabolic rate and that glial metabolic rate is a surrogate marker for 'neuroinflammation', our preliminary results suggest that [1-13C] MRS may provide biomarkers for diseases, believed to involve microglia and other cells of the astrocyte series. Among these is AD, for which novel drugs which ameliorate the damaging effects of neuroinflammation before symptoms of dementia appear, are in advanced development. The value of 13C MRS as an early, noninvasive biomarker may lie in the conduct of cost-effective clinical trials.Keywords: Alzheimer's disease, noninvasive biomarker, glial activation |
format |
article |
author |
Tran T Harris K Sailasuta N Ross B |
author_facet |
Tran T Harris K Sailasuta N Ross B |
author_sort |
Tran T |
title |
Minimally invasive biomarker confirms glial activation present in Alzheimer's disease: a preliminary study |
title_short |
Minimally invasive biomarker confirms glial activation present in Alzheimer's disease: a preliminary study |
title_full |
Minimally invasive biomarker confirms glial activation present in Alzheimer's disease: a preliminary study |
title_fullStr |
Minimally invasive biomarker confirms glial activation present in Alzheimer's disease: a preliminary study |
title_full_unstemmed |
Minimally invasive biomarker confirms glial activation present in Alzheimer's disease: a preliminary study |
title_sort |
minimally invasive biomarker confirms glial activation present in alzheimer's disease: a preliminary study |
publisher |
Dove Medical Press |
publishDate |
2011 |
url |
https://doaj.org/article/5ba6dcdf4ac942c3afd7e47b352ab4ae |
work_keys_str_mv |
AT trant minimallyinvasivebiomarkerconfirmsglialactivationpresentinalzheimeramp39sdiseaseapreliminarystudy AT harrisk minimallyinvasivebiomarkerconfirmsglialactivationpresentinalzheimeramp39sdiseaseapreliminarystudy AT sailasutan minimallyinvasivebiomarkerconfirmsglialactivationpresentinalzheimeramp39sdiseaseapreliminarystudy AT rossb minimallyinvasivebiomarkerconfirmsglialactivationpresentinalzheimeramp39sdiseaseapreliminarystudy |
_version_ |
1718401730438234112 |