Evidence map›Paper›PMID 27309537›Full record

Trial reportPloS one2016

N-Acetyl Cysteine May Support Dopamine Neurons in Parkinson's Disease: Preliminary Clinical and Cell Line Data.

Daniel A Monti, George Zabrecky, Daniel Kremens, Tsao-Wei Liang, Nancy A Wintering, Jingli Cai, Xiatao Wei, Anthony J Bazzan, Li Zhong, Brendan Bowen and 3 more

3 registry-linked trialsOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 95 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 6 pooled it
6.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02445651 nacompletednot on this map

Physiological Effects of Nutritional Support in Patients With Parkinson's Disease

TypeinterventionalSponsorThomas Jefferson UniversityRan2014 to 2022Enrolled51ConditionsParkinson Disease, Idiopathic Parkinson DiseaseArmsIntravenous and Oral n-acetyl cysteine, Control group, Oral Supplements: Baicalin, Ganoderma, Omega 3 and Curcumin
NCT04459052 phase2active not recruitingnot on this mapstarted 2020, after this paper: background citation

Phase II: Physiological Effects of Nutritional Support in Patients With Parkinson's Disease

TypeinterventionalSponsorThomas Jefferson UniversityRan2020 to 2027Enrolled50ConditionsParkinson Disease, Idiopathic Parkinson DiseaseArmsN acetyl cysteine, [F-18] Fluorodopa Positron Emission Tomography
NCT04562597 phase1 / phase2completednot on this mapstarted 2021, after this paper: background citation

A Pilot Trial to Determine the Effective Dose of N-acetylcysteine for Opioid Reduction in Patients Undergoing Spine Surgery.

TypeinterventionalSponsorMedical University of South CarolinaRan2021 to 2022Enrolled50ConditionsSurgeryArmsDose Response Curve Placebo, Dose Response Curve N-acetylcysteine 50 mg/kg, Dose Response Curve N-acetylcysteine 100 mg/kg, Dose Response Curve N-acetylcysteine 150 mg/kg, Opioid Reduction with Optimal N-acetylcysteine Dose
3 · Its place in the literature

Who cites it

95 citing papers in PubMed, 6 syntheses or guidelines pooled it, 145 citations in OpenAlex.

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35 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Daniel A MontiMyrna Brind Center of Integrative Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
George ZabreckyMyrna Brind Center of Integrative Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Daniel KremensMovement Disorders Center, Department of Neurology, Thomas Jefferson University, Philadelphia, PA, United States of America.
Tsao-Wei LiangMovement Disorders Center, Department of Neurology, Thomas Jefferson University, Philadelphia, PA, United States of America.
Nancy A WinteringMyrna Brind Center of Integrative Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Jingli CaiDepartment of Neuroscience, Thomas Jefferson University, Philadelphia, PA, United States of America.
Xiatao WeiDepartment of Neuroscience, Thomas Jefferson University, Philadelphia, PA, United States of America.
Anthony J BazzanMyrna Brind Center of Integrative Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Li ZhongMyrna Brind Center of Integrative Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Brendan BowenMyrna Brind Center of Integrative Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Charles M IntenzoDivision of Nuclear Medicine, Department of Radiology, Thomas Jefferson University, Philadelphia, PA, United States of America.
Lorraine IacovittiDepartment of Neuroscience, Thomas Jefferson University, Philadelphia, PA, United States of America.
Andrew B NewbergMyrna Brind Center of Integrative Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Thomas Jefferson University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgoundThe purpose of this study was to assess the biological and clinical effects of n-acetyl-cysteine (NAC) in Parkinson's disease (PD).

methodsThe overarching goal of this pilot study was to generate additional data about potentially protective properties of NAC in PD, using an in vitro and in vivo approach. In preparation for the clinical study we performed a cell tissue culture study with human embryonic stem cell (hESC)-derived midbrain dopamine (mDA) neurons that were treated with rotenone as a model for PD. The primary outcome in the cell tissue cultures was the number of cells that survived the insult with the neurotoxin rotenone. In the clinical study, patients continued their standard of care and were randomized to receive either daily NAC or were a waitlist control. Patients were evaluated before and after 3 months of receiving the NAC with DaTscan to measure dopamine transporter (DAT) binding and the Unified Parkinson's Disease Rating Scale (UPDRS) to measure clinical symptoms.

resultsThe cell line study showed that NAC exposure resulted in significantly more mDA neurons surviving after exposure to rotenone compared to no NAC, consistent with the protective effects of NAC previously observed. The clinical study showed significantly increased DAT binding in the caudate and putamen (mean increase ranging from 4.4% to 7.8%; p<0.05 for all values) in the PD group treated with NAC, and no measurable changes in the control group. UPDRS scores were also significantly improved in the NAC group (mean improvement of 12.9%, p = 0.01).

conclusionsThe results of this preliminary study demonstrate for the first time a potential direct effect of NAC on the dopamine system in PD patients, and this observation may be associated with positive clinical effects. A large-scale clinical trial to test the therapeutic efficacy of NAC in this population and to better elucidate the mechanism of action is warranted.

trial registrationClinicalTrials.gov NCT02445651.

Indexed as

AcetylcysteineAgedAntioxidantsCaudate NucleusCell DifferentiationCell SurvivalDopamineDopamine Plasma Membrane Transport ProteinsDopaminergic NeuronsFemaleHuman Embryonic Stem CellsHumansMaleMesencephalonMiddle AgedNeuroprotective AgentsAcetylcysteineAntioxidantsDopamineDopamine Plasma Membrane Transport ProteinsNeuroprotective AgentsNeurotoxinsRotenone

Identifiers

PMID27309537
PMCPMC4911055
OpenAlexW2439394256

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.