Evidence map›Paper›PMID 37798410›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2024

A 12-month prospective real-life study of opicapone efficacy and tolerability in Emirati and non-White subjects with Parkinson's disease based in United Arab Emirates.

Vinod Metta, Huzaifa Ibrahim, Neha Muralidharan, Kislyn Rodriguez, Therese Masagnay, Judith Mohan, Arlet Lacsina, Abdullah Ahmed, Hani T S Benamer, Guy Chung-Faye and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of neural transmission (Vienna, Austria : 1996), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 19% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Observational
  5. Article
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

17 authors at 8 institutions in 6 countries.

Vinod MettaKing's College London, Department of Neurosciences, Institute of Psychiatry, Psychology and Neuroscience and Parkinson's Foundation Centre of Excellence, King's College Hospital, London, UK. vinod.metta@nhs.net.ORCID 0000-0002-8970-8595
Huzaifa IbrahimParkinson's Association United Arab Emirates, Dubai, United Arab Emirates.
Neha MuralidharanParkinson's Foundation Centre of Excellence, King's College Hospital, Dubai, United Arab Emirates.
Kislyn RodriguezParkinson's Foundation Centre of Excellence, King's College Hospital, Dubai, United Arab Emirates.
Therese MasagnayParkinson's Foundation Centre of Excellence, King's College Hospital, Dubai, United Arab Emirates.
Judith MohanParkinson's Foundation Centre of Excellence, King's College Hospital, Dubai, United Arab Emirates.
Arlet LacsinaParkinson's Foundation Centre of Excellence, King's College Hospital, Dubai, United Arab Emirates.
Abdullah AhmedParkinson's Foundation Centre of Excellence, King's College Hospital, Dubai, United Arab Emirates.
Hani T S BenamerCollege of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Guy Chung-FayeKing's College London, Department of Neurosciences, Institute of Psychiatry, Psychology and Neuroscience and Parkinson's Foundation Centre of Excellence, King's College Hospital, London, UK.
Rukmini MrudulaNizams Institute of Medical Sciences, Hyderabad, Telangana, India.
Cristian Falup-PecurariuDepartment of Neurology, Transilvania University of Brasov, Brasov, Romania.
Carmen Rodriguez-BlazquezInstitute of Salud Carlos 111, Madrid, Spain.
Rupam BorgohainNizams Institute of Medical Sciences, Hyderabad, Telangana, India.
Vinay GoyalInstitute of Movement Disorders and Parkinson's Centre, Medanta Hospitals, Delhi, India.
Kalyan BhattacharyaR G Kar Medical College and Hospital, Kolkata, India.
K Ray ChaudhuriKing's College London, Department of Neurosciences, Institute of Psychiatry, Psychology and Neuroscience and Parkinson's Foundation Centre of Excellence, King's College Hospital, London, UK.
Parkinson's Foundation · USKing's College London · GBNizam's Institute of Medical Sciences · INEmirates Foundation · AEInstituto de Salud Carlos III · ESMohammed Bin Rashid University of Medicine and Health Sciences · AER. G. Kar Medical College and Hospital · INTransylvania University of Brașov · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is the second most common neurodegenerative disorder, and the condition is complicated by the emergence of wearing off/motor fluctuations with levodopa treatment after a variable period. COMT inhibitors when used as adjunct therapy to levodopa tend to smoothen out these wearing off fluctuations by enhancing delivery of levodopa and increasing its bioavailability to the brain. The study was conducted to investigate the motor and nonmotor effect, safety and tolerability of the third generation once-daily COMT inhibitor (opicapone), as add-on, adjuvant therapy to levodopa and at 6 and 12 months follow-up in a real-life cohort of consecutive Emirati and non-White PD patients. A real-life observational analysis using tolerability parameters as used previously by Rizos et al. and Shulman et al. based on clinical database of cases rat Kings College Hospital Dubai Parkinson care database. This was a prospective, single-arm follow-up clinical evaluation study that evaluated the effectiveness of opicapone 50 mg once-daily regime in 50 patients diagnosed with idiopathic neurodegenerative disorder. All patients were assessed with scales used in clinical pathway and include motor Unified Parkinson's Disease Rating Scale (UPDRS), nonmotor symptom scale (NMSS), quality of life (PDQ8) Parkinson's fatigue scale (PFS16) and King's Parkinson's Pain Scale (KIPS). Out of 50 patients treated with opicapone (72% male, mean age 66.9 years (SD 9.9, range 41-82 years) and mean duration of disease 5.7 years (SD 2.5 range (2-11), there was significant statistical improvements shown in motor function-UPDRS part 3: baseline 40.64 ± 2.7, at 6 months 32.12 ± 3.14 and after 12 months 33.72 ± 3.76. Nonmotor burden NMSS: 107.00 ± 21.86, at 6 months 100.78 ± 17.28 and 12 months 96.88 ± 16.11. Reduction in dyskinesias (UPDRS part 4): baseline 8.78 ± 1.07, at 6 months 7.4 ± 0.81 and 12 months 6.82 ± 0.75. Opicapone provides beneficial motor and nonmotor effects in Emirati and other non-White Parkinson's patients, resident in UAE, proving its efficacy across different racial groups as COMT activity may vary between races.

Indexed as

Parkinson DiseaseAdultAgedAged, 80 and overAnimalsAntiparkinson AgentsCatechol O-Methyltransferase InhibitorsFemaleHumansLevodopaMaleMiddle AgedOxadiazolesProspective StudiesQuality of LifeRatsAntiparkinson AgentsCatechol O-Methyltransferase InhibitorsLevodopaopicaponeOxadiazolesCatechol-O-methyltransferaseEntacaponeNonmotor symptomsOpicapone

Identifiers

PMID37798410
PMCPMC10769978
OpenAlexW4387362042

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.