A ferroptosis-based panel of prognostic biomarkers for
Amyotrophic Lateral Sclerosis

J 2019

A ferroptosis-based panel of prognostic biomarkers for Amyotrophic Lateral Sclerosis

DEVOS, D., C. MOREAU, M. KYHENG, G. GARCON, A. S. O. ROLLAND et. al.

Základní údaje

Originální název

A ferroptosis-based panel of prognostic biomarkers for Amyotrophic Lateral Sclerosis

Autoři

Vydání

Nature Scientific Reports, London, NATURE RESEARCH, 2019, 2045-2322

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30210 Clinical neurology

Stát vydavatele

Velká Británie a Severní Irsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

URL

Impakt faktor

Impact factor: 3.998

Kód RIV

RIV/00216224:14110/19:00121482

Organizační jednotka

Lékařská fakulta

DOI

http://dx.doi.org/10.1038/s41598-019-39739-5

UT WoS

000459799800067

Klíčová slova anglicky

Amyotrophic Lateral Sclerosis; prognostic biomarkers

Štítky

Excelence Science, INT, RIV, rivok, user

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 28. 4. 2021 09:29, Mgr. Tereza Miškechová

Anotace

V originále

Accurate patient stratification into prognostic categories and targeting Amyotrophic Lateral Sclerosis (ALS)-associated pathways may pave the way for promising trials. We evaluated blood-based prognostic indicators using an array of pathological markers. Plasma samples were collected as part of a large, phase III clinical trial (Mitotarget/TRO19622) at months 1, 6, 12 and 18. The ALSFRS-r score was used as a proxy of disease progression to assess the predictive value of candidate biological indicators. First, established clinical predictors were evaluated in all 512 patients. Subsequently, pathologic markers, such as proxies of neuronal integrity (Neurofilament light chain and phosphorylated heavy chain), DNA oxidation (8-oxo-2'-desoxyguanosine), lipid peroxidation (4-hydroxy-2-nonenal, isoprostane), inflammation (interleukin-6) and iron status (ferritin, hepcidin, transferrin) were assessed in a subset of 109 patients that represented the whole cohort. Markers of neuronal integrity, DNA and lipid oxidation, as well as iron status at baseline are accurate predictors of disability at 18-month follow-up. The composite scores of these markers in association with established clinical predictors enable the accurate forecasting of functional decline. The identified four biomarkers are all closely associated with 'ferroptosis', a recently discovered form of programmed cell death with promising therapeutic targets. The predictive potential of these pathophysiology-based indicators may offer superior patient stratification for future trials, individualised patient care and resource allocation.

Návaznosti

90090, velká výzkumná infrastruktura

Název: CZECRIN II

Citovat

DEVOS, D., C. MOREAU, M. KYHENG, G. GARCON, A. S. O. ROLLAND, H. BLASCO, P. GELE, T. T. LENGLET, C. VEYRAT-DUREBEX, P. CORCIA, M. DUTHEIL, P. BEDE, A. JEROMIN, P. OECKL, M. OTTO, V. MENINGER, V. DANEL-BRUNAUD, J. C. DEVEDJIAN, J. A. DUCE a P. F. PRADAT. A ferroptosis-based panel of prognostic biomarkers for Amyotrophic Lateral Sclerosis. Nature Scientific Reports. London: NATURE RESEARCH, 2019, roč. 9, FEB 2019, s. 1-6. ISSN 2045-2322. Dostupné z: https://dx.doi.org/10.1038/s41598-019-39739-5.

@article{1763937,
   author = {Devos, D. and Moreau, C. and Kyheng, M. and Garcon, G. and Rolland, A. S. O. and Blasco, H. and Gele, P. and Lenglet, T. T. and VeyratandDurebex, C. and Corcia, P. and Dutheil, M. and Bede, P. and Jeromin, A. and Oeckl, P. and Otto, M. and Meninger, V. and DanelandBrunaud, V. and Devedjian, J. C. and Duce, J. A. and Pradat, P. F.},
   article_location = {London},
   article_number = {FEB 2019},
   doi = {http://dx.doi.org/10.1038/s41598-019-39739-5},
   keywords = {Amyotrophic Lateral Sclerosis; prognostic biomarkers},
   language = {eng},
   issn = {2045-2322},
   journal = {Nature Scientific Reports},
   title = {A ferroptosis-based panel of prognostic biomarkers for Amyotrophic Lateral Sclerosis},
   url = {https://www.nature.com/articles/s41598-019-39739-5.pdf},
   volume = {9},
   year = {2019}
}

TY  - JOUR
ID  - 1763937
AU  - Devos, D. - Moreau, C. - Kyheng, M. - Garcon, G. - Rolland, A. S. O. - Blasco, H. - Gele, P. - Lenglet, T. T. - Veyrat-Durebex, C. - Corcia, P. - Dutheil, M. - Bede, P. - Jeromin, A. - Oeckl, P. - Otto, M. - Meninger, V. - Danel-Brunaud, V. - Devedjian, J. C. - Duce, J. A. - Pradat, P. F.
PY  - 2019
TI  - A ferroptosis-based panel of prognostic biomarkers for Amyotrophic Lateral Sclerosis
JF  - Nature Scientific Reports
VL  - 9
IS  - FEB 2019
SP  - 1-6
EP  - 1-6
PB  - NATURE RESEARCH
SN  - 20452322
KW  - Amyotrophic Lateral Sclerosis
KW  - prognostic biomarkers
UR  - https://www.nature.com/articles/s41598-019-39739-5.pdf
N2  - Accurate patient stratification into prognostic categories and targeting Amyotrophic Lateral Sclerosis (ALS)-associated pathways may pave the way for promising trials. We evaluated blood-based prognostic indicators using an array of pathological markers. Plasma samples were collected as part of a large, phase III clinical trial (Mitotarget/TRO19622) at months 1, 6, 12 and 18. The ALSFRS-r score was used as a proxy of disease progression to assess the predictive value of candidate biological indicators. First, established clinical predictors were evaluated in all 512 patients. Subsequently, pathologic markers, such as proxies of neuronal integrity (Neurofilament light chain and phosphorylated heavy chain), DNA oxidation (8-oxo-2'-desoxyguanosine), lipid peroxidation (4-hydroxy-2-nonenal, isoprostane), inflammation (interleukin-6) and iron status (ferritin, hepcidin, transferrin) were assessed in a subset of 109 patients that represented the whole cohort. Markers of neuronal integrity, DNA and lipid oxidation, as well as iron status at baseline are accurate predictors of disability at 18-month follow-up. The composite scores of these markers in association with established clinical predictors enable the accurate forecasting of functional decline. The identified four biomarkers are all closely associated with 'ferroptosis', a recently discovered form of programmed cell death with promising therapeutic targets. The predictive potential of these pathophysiology-based indicators may offer superior patient stratification for future trials, individualised patient care and resource allocation.
ER  -

DEVOS, D., C. MOREAU, M. KYHENG, G. GARCON, A. S. O. ROLLAND, H. BLASCO, P. GELE, T. T. LENGLET, C. VEYRAT-DUREBEX, P. CORCIA, M. DUTHEIL, P. BEDE, A. JEROMIN, P. OECKL, M. OTTO, V. MENINGER, V. DANEL-BRUNAUD, J. C. DEVEDJIAN, J. A. DUCE a P. F. PRADAT. A ferroptosis-based panel of prognostic biomarkers for Amyotrophic Lateral Sclerosis. \textit{Nature Scientific Reports}. London: NATURE RESEARCH, 2019, roč.~9, FEB 2019, s.~1-6. ISSN~2045-2322. Dostupné z: https://dx.doi.org/10.1038/s41598-019-39739-5.

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