Articles with "oprm1 rs1799971" as a keyword



Association of OPRM1 rs1799971, HTR1B rs6296 and COMT rs4680 polymorphisms with clinical phenotype among women with fibromyalgia

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Published in 2024 at "Scientific Reports"

DOI: 10.1038/s41598-024-62240-7

Abstract: To investigate the association between three selected pain polymorphisms and clinical, functional, sensory-related, psychophysical, psychological or cognitive variables in a sample of women with fibromyalgia (FMS). One hundred twenty-three (n = 123) women with FMS completed demographic… read more here.

Keywords: htr1b rs6296; comt rs4680; oprm1 rs1799971;

OPRM1 rs1799971 - COMT rs4680 - FAAH rs324420 genes interact with placebo procedures to induce hypoalgesia.

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Published in 2019 at "Pain"

DOI: 10.1097/j.pain.0000000000001578

Abstract: Genetics studies on the placebo hypoalgesic effect highlight a promising link between single nucleotide polymorphisms (SNPs) in the dopamine, opioid, and endocannabinoid genes and placebo hypoalgesia. However, epistasis and replication studies are missing. In this… read more here.

Keywords: comt; rs324420 genes; oprm1 rs1799971; faah rs324420 ... See more keywords

Association of Genetic Variants, Such as the μ-Opioid Receptor 1 (OPRM1) rs1799971 and Catechol-O-Methyltransferase (COMT) rs4680, with Phenotypic Expression of Fibromyalgia

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Published in 2025 at "Biomedicines"

DOI: 10.3390/biomedicines13051183

Abstract: Background/Objectives: Genetic variants, such as the µ-opioid receptor 1 (OPRM1) rs1799971 and the catechol-O-methyltransferase (COMT) rs4680, have been considered among the potential causes in the development of some chronic pain conditions. In this regard, there… read more here.

Keywords: comt rs4680; comt; genetic variants; oprm1 rs1799971 ... See more keywords