Cerebrospinal Fluid Levels of Chromogranin A in Parkinson's Disease and Multiple System Atrophy
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
Institutional Support 2020 - conceptual development of a research organization (FNOl, 0098892.)
Ministerstvo Zdravotnictví Ceské Republiky
European Regional Development Fund - Project ENOCH (No. Z.02.1.01/0.0/0.0/16_019/0000868)
Ministerstvo Školství, Mládeže a Tělovýchovy
PubMed
33499181
PubMed Central
PMC7912438
DOI
10.3390/brainsci11020141
PII: brainsci11020141
Knihovny.cz E-zdroje
- Klíčová slova
- Parkinson’s disease, cerebrospinal fluid, chromogranin A, multiple system atrophy,
- Publikační typ
- časopisecké články MeSH
BACKGROUND: Chromogranin A (CgA) and other peptides from the chromogranin-secretogranin family have been recently studied as potential biomarkers of various neurodegenerative diseases, including Parkinson's disease (PD). METHODS: We measured CgA in the cerebrospinal fluid (CSF) of 119 PD patients, 18 multiple system atrophy (MSA) patients, and 31 age-matched controls. We also correlated the values with disease duration and levodopa dose equivalent. RESULTS: In the PD patients, CSF CgA tended to be lower than the control group (median 124.5 vs. 185.2 µg/L; p = 0.057); however, the results did not reach statistical significance. CSF CgA levels in MSA were significantly lower compared to the control group (median 104.4 vs. 185.2; p = 0.014). There was no significant difference in CSF CgA between PD and MSA patients (p = 0.372). There was no association between CSF CgA and disease duration or levodopa dose equivalent in PD or in MSA. CONCLUSIONS: We observed a tendency toward lower CSF CgA levels in both PD and MSA compared to the control group; however, the difference reached statistical significance only in MSA. Based on these results, CgA may have potential as a biomarker in PD and MSA, but further studies on larger numbers of patients are needed to draw conclusions.
Department of Neurology University Hospital Olomouc 1 P Pavlova 6 77900 Olomouc Czech Republic
Institute of Biomedical Sciences Faculty of Medicine Ostrava University 70103 Ostrava Czech Republic
Institute of Laboratory Diagnostics University Hospital Ostrava 70103 Ostrava Czech Republic
Neurology Outpatient Clinic St Moritz 77900 Olomouc Czech Republic
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Taupenot L., Harper K.L., O’Connor D.T. The chromogranin-secretogranin family. N. Engl. J. Med. 2003;348:1134–1149. doi: 10.1056/NEJMra021405. PubMed DOI
Nobels F.R.E., Kwekkeboom D.J., Bouillon R., Lamberts S.W.J. Chromogranin A: Its clinical value as marker of neuroendocrine tumours. Eur. J. Clin. Investig. 1998;28:431–440. doi: 10.1046/j.1365-2362.1998.00305.x. PubMed DOI
Sahu B.S., Sonawane P.J., Mahapatra N.R. Chromogranin A: A novel susceptibility gene for essential hypertension. Cell. Mol. Life Sci. 2010;67:861–874. doi: 10.1007/s00018-009-0208-y. PubMed DOI PMC
Pedrero-Prieto C.M., Garcia-Carpintero S., Frontinan-Rubio J., Llanos-Gonzalez E., Garcia C.A., Alcain F.J., Lindberg I., Duran-Prado M., Peinado J.R., Rabanal-Ruiz Y. A comprehensive systematic review of CSF proteins and peptides that define Alzheimer’s disease. Clin. Proteom. 2020;17:1–24. doi: 10.1186/s12014-020-09276-9. PubMed DOI PMC
Kaiserova M., Grambalova Z., Otruba P., Stejskal D., Vranova H.P., Mares J., Mensikova K., Kanovsky P. Cerebrospinal fluid levels of chromogranin A and phosphorylated neurofilament heavy chain are elevated in amyotrophic lateral sclerosis. Acta Neurol Scand. 2017;136:360–364. doi: 10.1111/ane.12735. PubMed DOI
Gmitterova K., Varges D., Schmitz M., Zafar S., Maass F., Lingor P., Zerr I. Chromogranin A Analysis in the Differential Diagnosis Across Lewy Body Disorders. J. Alzheimers Dis. 2020;73:1355–1361. doi: 10.3233/JAD-191153. PubMed DOI
Kaiserova M., Vranova H.P., Galuszka J., Stejskal D., Mensikova K., Zapletalova J., Mares J., Kanovsky P. Orthostatic hypotension is associated with decreased cerebrospinal fluid levels of chromogranin A in early stage of Parkinson disease. Clin. Auton. Res. 2015;25:339–342. doi: 10.1007/s10286-015-0302-1. PubMed DOI
Kaiserova M., Vranova H.P., Stejskal D., Mensikova K., Kanovsky P. Cerebrospinal fluid levels of chromogranin A in the treatment-naïve early stage Parkinson’s disease: A pilot study. J. Neural Transm. 2013;120:1559–1563. doi: 10.1007/s00702-013-1020-2. PubMed DOI
Xu D.J., Wei L.Y., Li H.F., Zhang W.Q. Serum levels of chromogranins and secretogranins correlate with the progress and severity of Parkinson’s disease. Kaohsiung J. Med. Sci. 2019;35:146–150. doi: 10.1002/kjm2.12026. PubMed DOI PMC
Oconnor D.T., Cervenka J.H., Stone R.A., Parmer R.J., Francobourland R.E., Madrazo I., Langlais P.J. Chromogranin-a Immunoreactivity in Human Cerebrospinal-Fluid-Properties, Relationship to Noradrenergic Neuronal-Activity, and Variation in Neurologic Disease. Neuroscience. 1993;56:999–1007. doi: 10.1016/0306-4522(93)90146-7. PubMed DOI
Rotunno M.S., Lane M., Zhang W.F., Wolf P., Oliva P., Viel C., Wills A.M., Alcalay R.N., Scherzer C.R., Shihabuddin L.S., et al. Cerebrospinal fluid proteomics implicates the granin family in Parkinson’s disease. Sci. Rep. 2020;10:2479. doi: 10.1038/s41598-020-59414-4. PubMed DOI PMC
Gibb W.R., Lees A.J. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson’s disease. J. Neurol. Neurosurg. Psychiatry. 1988;51:745–752. doi: 10.1136/jnnp.51.6.745. PubMed DOI PMC
Gilman S., Wenning G., Low P., Brooks D., Mathias C., Trojanowski J., Wood N.W., Colosimo C., Durr A., Fowler C., et al. Second consensus statement on the diagnosis of multiple system atrophy. Neurology. 2008;70:A229. doi: 10.1212/01.wnl.0000324625.00404.15. PubMed DOI PMC
Modlin I.M., Gustafsson B.I., Steven F Moss S.M., Pavel M., Tsolakis A.V., Kidd M. Chromogranin A—Biological function and clinical utility in neuro endocrine tumor disease. Ann. Surg. Oncol. 2010;17:2427–2443. doi: 10.1245/s10434-010-1006-3. PubMed DOI
Benarroch E.E. Brainstem in multiple system atrophy: Clinicopathological correlations. Cell Mol. Neurobiol. 2003;23:519–526. doi: 10.1023/A:1025067912199. PubMed DOI PMC