Evidence map›Paper›PMID 40629324›Full record

ReviewJournal of translational medicine2025

Recent advances in targeting LRRK2 for Parkinson's disease treatment.

Mahsa Karami, Pantea Majma Sanaye, Atousa Ghorbani, Roshanak Amirian, Pouya Goleij, Mehregan Babamohamadi, Zhila Izadi

Abstract readReview
In one paragraph

Review in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Bridging Genetics and Precision Medicine in Parkinson's Disease through GP2.medRxiv : the preprint server for health sciences · 2026
    Article
  6. Article
  7. Review
  8. LRRK2 as a Potential Disease-Modifying Target in Sporadic Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2026
    Review
  9. Review
  10. Review
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

7 authors.

Mahsa Karami *Student Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Pantea Majma Sanaye *Pharmaceutical Sciences Research Center, Health Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Atousa GhorbaniUSERN Office, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Roshanak AmirianStudent Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Pouya GoleijUSERN Office, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Mehregan BabamohamadiUSERN Office, Kermanshah University of Medical Sciences, Kermanshah, Iran. mehregan.babamohamadi99@gmail.com.
Zhila IzadiPharmaceutical Sciences Research Center, Health Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran. izadi.zhila@yahoo.com.ORCID 0000-0002-4546-5202

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is a neurodegenerative disease with severe movement problems. Current treatments mainly focus on symptom management by reducing dopaminergic pathways in the brain. Despite these therapies, ongoing disease progression undermines the effectiveness of prevalent approaches, necessitating exploring alternative methods anchored on genetic factors, notably the leucine-rich repeat kinase 2 (LRRK2) gene. Exploring LRRK2 gene pathogenesis has highlighted various mechanisms that may contribute to treating PD, including protein accumulation, altered cytoskeletal dynamics, neuro-inflammation, autophagy, and mitochondrial dysfunction. Based on the findings, there is an actual correlation between elevated levels of LRRK2 and the biomarkers and assays of PD. Furthermore, research results have suggested inhibiting LRRK2 as a therapeutic intervention targeting pathogenic mechanisms with varying degrees of efficacy. Our review wants to understand how LRRK2 works in the body and its relationship with the occurrence of PD by providing biochemical evidence, LRRK2 gene mutations and pathology, and the role of this gene in the immune system. We also discuss targeted therapies such as kinase inhibitors and Proteolysis targeting chimera and the application of using the LRRK2 protein to diagnose PD and develop bioassay designs. Finally, we mention the clinical trials conducted and the challenges and safety required.

Indexed as

Leucine-Rich Repeat Serine-Threonine Protein Kinase-2Molecular Targeted TherapyParkinson DiseaseAnimalsClinical Trials as TopicHumansMutationLeucine-Rich Repeat Serine-Threonine Protein Kinase-2LRRK2 protein, humanAutophagyLRRK2Mitochondrial dysfunctionNeurodegenerative diseasesNeuro-inflammationParkinson’s diseasePROTAC

Identifiers

PMID40629324
PMCPMC12235878

What OpenQuestion holds

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Registered trials

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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.