4.3 Article

Plasma near-infrared spectroscopy for diagnosis of idiopathic Parkinson's disease: the SPIN-PD study

Journal

BIOMARKERS IN MEDICINE
Volume 9, Issue 2, Pages 89-97

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/BMM.14.103

Keywords

biomarker; diagnosis; near-infrared spectroscopy; oxidative stress; Parkinson's disease; plasma

Funding

  1. Michael J Fox Foundation
  2. NIH
  3. Biogen Idec
  4. Auspex Pharmaceuticals
  5. Department of Defense
  6. Prana Biotechnology, Ltd
  7. Sanofi
  8. Brain Canada
  9. Canadian Institutes of Health Research
  10. Edmond J Safra Philanthropic Foundation
  11. National Parkinson Foundation
  12. Parkinson Society Canada
  13. Tourette Syndrome Association
  14. W Garfield Weston Foundation

Ask authors/readers for more resources

Aim: There are no established chemical biomarkers of idiopathic Parkinson's disease (PD). The results of a prior metabolomics-based biomarker study suggested that near-infrared spectroscopy of blood plasma samples may distinguish idiopathic PD from neurologically normal controls. Methods: Near-infrared spectroscopy was used to detect and quantify substrate modifications in blood plasma samples derived from 71 PD subjects enrolled in the PostCEPT observational study and 68 normal control subjects. Results: Near-infrared spectra values were significantly higher in the PD group compared with the control group when adjusted for age and gender (PD: adjusted mean 0.49 [95% CI: 0.45-0.53]; control: adjusted mean 0.40 [95% CI: 0.36-0.44]; p = 0.004, multiple regression). Conclusion: Near-infrared spectra of blood plasma in early-stage idiopathic PD differ from those of non-neurological control subjects. However, the degree of overlap between the groups limits the use of this technique in its present form as a PD biomarker for routine clinical practice.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Letter Clinical Neurology

Combining Skin α-Synuclein Real-Time Quaking-Induced Conversion and Circulating Neurofilament Light Chain to Distinguish Multiple System Atrophy and Parkinson's Disease

Ivan Martinez-Valbuena, Naomi P. Visanji, Diana A. Olszewska, Mario Sousa, Puja Bhakta, Anna Vasilevskaya, Chloe Anastassiadis, Maria Carmela Tartaglia, Gabor G. Kovacs, Anthony E. Lang

MOVEMENT DISORDERS (2022)

Article Clinical Neurology

Longitudinal evaluations of somatosensory-motor inhibition in Dopa-responsive dystonia

Anne Weissbach, Annika Steinmeier, Martje Pauly, Duha M. Al-Shorafat, Gerard Saranza, Anthony Lang, Norbert Brueggemann, Vera Tadic, Christine Klein, Alexander Muenchau, Tobias Baeumer, Matt J. N. Brown

Summary: This study examined sensorimotor inhibition in GCH1 mutation carriers and found that their short-latency afferent inhibition (SAI) and dual-site transcranial magnetic stimulation (ds-TMS) levels were not significantly different from the control group. However, SAI decreased over time in mutation carriers off dopamine replacement therapy (DRT). These results suggest changes in plasticity in the sensorimotor networks.

PARKINSONISM & RELATED DISORDERS (2022)

Article Clinical Neurology

Oculogyric Crisis Phenotype of Levodopa-Induced Ocular Dyskinesia

Diana A. Olszewska, Rajesh Shetty, Thenral S. Geetha, Vedam L. Ramprasad, Anthony E. Lang, Prashanth Lingappa Kukkle

MOVEMENT DISORDERS CLINICAL PRACTICE (2022)

Letter Clinical Neurology

CBD diagnostic criteria: exclusions as important as inclusions

Irene Litvan, Anthony E. Lang, Melissa Armstrong

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2023)

Letter Clinical Neurology

Dystonia with myoclonus and vertical supranuclear gaze palsy associated with a rare GNB1 variant

Nikolai Gil D. Reyes, Daniel G. Di Luca, Vanda McNiven, Anthony E. Lang

Summary: GNB1 encephalopathy is a rare neuro-developmental syndrome caused by pathogenic variants in the GNB1 gene. It is characterized by global developmental delay and co-occurrence of movement disorders, with dystonia being the most common. Other rare phenomenologies include myoclonus, tics, chorea, ataxia, and oculomotor abnormalities. This case report presents a unique phenotype of GNB1 encephalopathy caused by a de novo mutation in exon 11, with symptoms of dystonia, myoclonus, and vertical supranuclear gaze palsy.

PARKINSONISM & RELATED DISORDERS (2023)

Letter Clinical Neurology

Isolated Dystonia as an Initial Presentation of GDAP2-Related Disorder

Daniel G. Di Luca, Dilinuer Wubuli, Vanda McNiven, Anthony E. Lang

MOVEMENT DISORDERS CLINICAL PRACTICE (2023)

Article Clinical Neurology

Distinguishing functional from primary tics: a study of expert video assessments

Antigony Rigas, Tina Mainka, Tamara Pringsheim, Alexander Muenchau, Irene Malaty, Yulia Worbe, Andrea E. Cavanna, Andrew John Lees, Anthony E. Lang, Davide Martino, Christos Ganos

Summary: This study revealed that the diagnostic distinction between primary and functional tics is often difficult, even for expert clinicians, in the absence of clinical information.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2023)

Article Clinical Neurology

The Lessebo Effect in Disease Modification Trials in Parkinson's Disease

Tiago A. Mestre, Michael P. McDermott, Raquel Lobo, Joaquim J. Ferreira, Anthony E. E. Lang

Summary: This study evaluated the "lessebo effect" in disease modification trials in Parkinson's disease and found that it did not exist in these trials. However, the use of placebo instead of an active comparator was a limitation. Prospective measurement of expectation of benefit could help assess the various impacts of placebo use.

MOVEMENT DISORDERS (2023)

Letter Clinical Neurology

Targeting alpha-Synuclein: A Further Viewpoint

Anthony E. Lang

MOVEMENT DISORDERS (2023)

Article Clinical Neurology

Classification and staging of Parkinson's disease using video-based eye tracking

Donald C. Brien, Heidi C. Riek, Rachel Yep, Jeff Huang, Brian Coe, Corson Areshenkoff, David Grimes, Mandar Jog, Anthony Lang, Connie Marras, Mario Masellis, Paula McLaughlin, Alicia Peltsch, Angela Roberts, Brian Tan, Derek Beaton, Wendy Lou, Richard Swartz, Douglas P. Munoz

Summary: A simple and non-invasive test was developed using video-based eye tracking and machine learning, which showed high sensitivity in detecting the stages of Parkinson's Disease and cognitive impairment. The classifier reached a sensitivity of 83% and a specificity of 78%.

PARKINSONISM & RELATED DISORDERS (2023)

Editorial Material Clinical Neurology

Adult-Onset Tourettism in SLC20A2-Associated Primary Familial Brain Calcification

Nikolai Gil D. Reyes, Anthony E. Lang

MOVEMENT DISORDERS CLINICAL PRACTICE (2023)

Letter Clinical Neurology

Familial Hypermanganesemia in Iran

Seyedeh Narges Tabatabaee, Sajjad Effat Nejad, Ali Nikkhah, Narges Hashemi, Afagh Alavi, Anthony E. E. Lang, Mohammad Rohani, Maziar Emamikhah

MOVEMENT DISORDERS CLINICAL PRACTICE (2023)

Article Clinical Neurology

Deep Brain Stimulation of the Globus Pallidus Internus and Externus in Multiple System Atrophy

Daniel G. Di Luca, Carolina Ramirez-Gomez, Jurgen Germann, Brendan Santyr, Alexandre Boutet, Luka Milosevic, Anthony E. Lang, Suneil K. Kalia, Andres M. Lozano, Alfonso Fasano

Summary: This study aimed to evaluate the safety and efficacy of deep brain stimulation on the globus pallidus pars interna and externa in MSA-P patients. The surgery did not result in major complications, but did not provide significant clinical benefit as measured by MDS-UPDRS III.

MOVEMENT DISORDERS (2023)

Review Clinical Neurology

Amantadine-Induced Craniofacial Myoclonus: Distinctive Iatrogenic Dysarthria in Parkinson's Disease

Iris Lin, Laura Armengou-Garcia, Sanskriti Sasikumar, Greg Kuhlman, Susan H. Fox, Anthony E. Lang, Alberto J. Espay

Summary: Speech-induced craniofacial myoclonus with stuttering-like dysarthria and speech arrests is a disabling iatrogenic complication in Parkinson's disease that resolves upon amantadine discontinuation. Four of the patients with renal insufficiency were identified as a risk factor.

MOVEMENT DISORDERS CLINICAL PRACTICE (2023)

Article Clinical Neurology

Estimation of Ambulation and Survival in Neurodegeneration with Brain Iron Accumulation Disorders

Elahe Amini, Mohammad Rohani, Anthony E. Lang, Zahra Azad, Seyed Amir Hassan Habibi, Afagh Alavi, Gholamali Shahidi, Maziar Emamikhah, Ahmad Chitsaz

Summary: Among 122 genetically confirmed NBIA patients, KRS had the best survival and longest preservation of ambulation ability, while classical PKAN and MPAN patients showed similar progression patterns in loss of ambulation ability, with MPAN patients having a slower progression to death. Spasticity was identified as the most significant factor associated with death.

MOVEMENT DISORDERS CLINICAL PRACTICE (2023)

No Data Available