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Proenkephalin Decreases in Cerebrospinal Fluid with Symptom Progression of Huntington's Disease

Niemelä, Valter (author)
Uppsala universitet,Landtblom: Neurovetenskap
Landtblom, Anne-Marie (author)
Uppsala universitet,Landtblom: Neurovetenskap
Nyholm, Dag (author)
Uppsala universitet,Landtblom: Neurovetenskap
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Kneider, Maria (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi,Institute of Neuroscience and Physiology,Institute of Neuroscience and Physiology; Clinical Neuroscience, The Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
Constantinescu, Radu, 1966 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi,Institute of Neuroscience and Physiology,Institute of Neuroscience and Physiology; Clinical Neuroscience, The Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
Paucar, M. (author)
Karolinska Institutet,Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
Svenningsson, P. (author)
Karolinska Institutet,Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
Abujrais, Sandy (author)
Uppsala universitet,Klinisk kemi
Burman, Joachim, 1974- (author)
Uppsala universitet,Landtblom: Neurovetenskap
Shevchenko, Ganna (author)
Uppsala universitet,Analytisk kemi
Bergquist, Jonas (author)
Uppsala universitet,Analytisk kemi
Sundblom, Jimmy, 1981- (author)
Uppsala universitet,Enblad: Neurokirurgi
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 (creator_code:org_t)
2020-11-28
2021
English.
In: Movement Disorders. - : Wiley. - 0885-3185 .- 1531-8257. ; 36:2, s. 481-491
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Objective Identifying molecular changes that contribute to the onset and progression of Huntington's disease (HD) is of importance for the development and evaluation of potential therapies. Methods We conducted an unbiased mass-spectrometry proteomic analysis on the cerebrospinal fluid of 12 manifest HD patients (ManHD), 13 pre-manifest (preHD), and 38 controls. A biologically plausible and significant possible biomarker was validated in samples from a separate cohort of patients and controls consisting of 23 ManHD patients and 23 controls. Results In ManHD compared to preHD, 10 proteins were downregulated and 43 upregulated. Decreased levels of proenkephalin (PENK) and transthyretin were closely linked to HD symptom severity, whereas levels of 15 upregulated proteins were associated with symptom severity. The decreased PENK levels were replicated in the separate cohort where absolute quantitation was performed. Conclusions We hypothesize that declining PENK levels reflect the degeneration of medium spiny neurons (MSNs) that produce PENK and that assays for PENK may serve as a surrogate marker for the state of MSNs in HD. (c) 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Keyword

s disease
biomarkers
proenkephalin
proteomics
protein
activation
plasma
onset
reveals
peptide
neurons
system
Neurosciences & Neurology
Huntington's disease

Publication and Content Type

ref (subject category)
art (subject category)

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