ReviewCureus2025
Interaction of Smoking and Genetic Polymorphisms in the Dopaminergic Pathway in Relation to Parkinson's Disease: A Scoping Review.
Review in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The inverse association of Parkinson's disease (PD) and smoking has been well established, but it is rarely investigated in the context of the different genetic backgrounds of the patients. This scoping review aims to comprehensively review the literature on the interactions of different essential genes involved in the dopaminergic pathway with smoking and how they modulate the risk of PD with smoking. A search using the keywords and abbreviations of smoking, genetic polymorphism, and parkinsonism was conducted in Web of Science, PubMed, Cochrane, and Scopus databases. References were retrieved and screened by two authors independently. Eleven human studies were included with 5131 cases and 7542 control adult populations with a male predominance (>60%) and multiethnic groups, mainly European origin populations. Most gene polymorphisms showed no modulation of the smoking-PD risk. Nevertheless, the risk was shown to change with MAO-B rs1799836 gene polymorphism in three studies where the G allele was associated with smoking protection against PD in 16.5% and 13.14% of cases and controls, respectively. While the COMT rs4680 polymorphism was suggested to interact with smoking in one study with 238 (37.9%) cases and 369 (31.5%) controls (p-value = 0.061), the effect of smoking on PD risk varied significantly with different SV2C (rs30196 and rs10214163) genotypes. Our study revealed the complexity of genetic polymorphism in the smoking-PD relationship. This explores the possibility of further research with larger sample sizes, accounting for different ethnic groups, to establish definitive links that can aid in treatment and prevention strategies.
Indexed as
Identifiers
What OpenQuestion holds
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.