# Efficacy of MAO-B and COMT inhibitors on quality of life in patients with Parkinson’s disease: a Bayesian network meta-analysis

**Authors:** Sung Ryul Shim, Yu Jin Jung, Kyum-Yil Kwon, Taeho Greg Rhee, Seon-Min Lee

PMC · DOI: 10.3389/fneur.2026.1753555 · Frontiers in Neurology · 2026-02-04

## TL;DR

This study compares how MAO-B and COMT inhibitors affect the quality of life in Parkinson’s disease patients, finding that rasagiline and safinamide offer the most benefits.

## Contribution

The study provides the first Bayesian network meta-analysis comparing MAO-B and COMT inhibitors' effects on quality of life in Parkinson’s disease.

## Key findings

- Extended-release rasagiline with pramipexole showed the most significant improvement in global quality of life.
- Safinamide 100 mg significantly improved emotional well-being in Parkinson’s patients.
- Rasagiline-based treatments ranked highest for quality of life benefits across multiple domains.

## Abstract

Quality of life (QoL) is a critical outcome in the management of Parkinson’s disease (PD), and is often affected more by non-motor symptoms (NMS) than motor features. While monoamine oxidase-B (MAO-B) and catechol-O-methyltransferase (COMT) inhibitors are commonly used with levodopa, their comparative impacts on QoL remains unclear. This study aimed to compare the effects of MAO-B and COMT inhibitors on global and domain-specific QoL in patients with PD using a Bayesian network meta-analysis (NMA).

A comprehensive literature search was conducted using PubMed/Medline, Cochrane Library and Embase databases from the inception through April 30, 2025. Randomized controlled trials evaluating QoL using PDQ-39 or PDQ-8 in patients treated with MAO-B inhibitors (rasagiline, selegiline, safinamide) or COMT inhibitors (entacapone, opicapone, tolcapone) were included. A Bayesian NMA was performed using the “gemtc” package in R. Treatment effects were expressed as standardized mean differences (SMDs) with 95% credible intervals (CrIs). Treatment ranking was estimated using surface under the cumulative ranking curve (SUCRA) values.

Sixteen RCTs comprised of 3,802 patients were included. The combination of extended-release rasagiline and pramipexole (P2B001) showed the most significant improvement in global QoL (SMD = −4.16; 95% CrI: −7.24 to −1.05), followed by rasagiline monotherapy (SMD = −2.38; 95% CrI: −4.32 to −0.42). Safinamide 100 mg significantly improved emotional well-being (SMD = −2.56; 95% CrI: −5.13 to −0.04). SUCRA rankings confirmed the superior probability of benefits for rasagiline-based interventions across multiple QoL dimensions.

This network meta-analysis provides evidence that MAO-B inhibitors, particularly rasagiline and safinamide, may offer broader QoL benefits in patients with PD, especially in NMS such as emotional well-being. These findings support a more symptom-oriented and individualized treatment approach should be provided to patients with PD. Further well-designed head-to-head studies using standardized QoL measures and extended follow-up are needed to confirm these findings and guide clinical practice.

Registered in PROSPERO (CRD420251013028): https://www.crd.york.ac.uk/PROSPERO/view/CRD420251013028

## Linked entities

- **Chemicals:** rasagiline (PubChem CID 122316), selegiline (PubChem CID 5195), safinamide (PubChem CID 131682), entacapone (PubChem CID 5281081), opicapone (PubChem CID 135565903), tolcapone (PubChem CID 4659569), pramipexole (PubChem CID 4885)
- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Genes:** COMT (catechol-O-methyltransferase) [NCBI Gene 1312] {aka HEL-S-98n}, MAOB (monoamine oxidase B) [NCBI Gene 4129]
- **Diseases:** mood and sleep disturbances (MESH:D019964), fatigue (MESH:D005221), neuropsychiatric symptoms (MESH:D001523), neurodegenerative disorder (MESH:D019636), pain (MESH:D010146), sleep disturbances (MESH:D012893), PD (MESH:D010300), rigidity (MESH:D009127), cognitive impairment (MESH:D003072), NMS (MESH:D020879), motor and non-motor symptoms (MESH:D000068079), dyskinesia (MESH:D004409), depression (MESH:D003866), glutamate excitotoxicity (MESH:C537425), impaired QoL (MESH:D003643), bradykinesia (MESH:D018476), tremor (MESH:D014202)
- **Chemicals:** amphetamine (MESH:D000661), glutamate (MESH:D018698), dopamine (MESH:D004298), Safinamide (MESH:C092797), selegiline (MESH:D012642), Rasagiline (MESH:C031967), entacapone (MESH:C071192), pramipexole (MESH:D000077487), P2B001 (-), opicapone (MESH:C549349), Levodopa (MESH:D007980), tolcapone (MESH:D000077867)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12913192/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913192/full.md

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Source: https://tomesphere.com/paper/PMC12913192