HUMAN STUDY
PainReportIt
Polymorphism
haploblock
healthcare
linkage disequilibrium
Journal
Experimental biology and medicine (Maywood, N.J.)
ISSN: 1535-3699
Titre abrégé: Exp Biol Med (Maywood)
Pays: England
ID NLM: 100973463
Informations de publication
Date de publication:
09 2022
09 2022
Historique:
pubmed:
15
3
2022
medline:
12
10
2022
entrez:
14
3
2022
Statut:
ppublish
Résumé
A previous exploratory analysis of a COMT gene single-nucleotide polymorphism (SNP) and a DRD3 SNP by our group suggested possible contributions to pain-related acute care utilization in people with sickle cell disease (SCD). Our aim was to extend the analysis to gene-spanning haplotypes of COMT SNPs and DRD3 SNPs to investigate possible associations with pain intensity and pain-related acute care utilization in an SCD cohort. Genotyping was conducted, and clinical data were collected, including self-reported pain intensity using PAINReportIt
Identifiants
pubmed: 35285297
doi: 10.1177/15353702221080716
pmc: PMC9554168
doi:
Substances chimiques
Catechol O-Methyltransferase
EC 2.1.1.6
COMT protein, human
EC 2.1.1.6
DRD3 protein, human
0
Receptors, Dopamine D3
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
1601-1608Subventions
Organisme : NHLBI NIH HHS
ID : R13 HL106871
Pays : United States
Organisme : NIA NIH HHS
ID : T32 AG049673
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL078536
Pays : United States
Organisme : NHLBI NIH HHS
ID : K01 HL153210
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA233444
Pays : United States
Organisme : NHLBI NIH HHS
ID : R35 HL140031
Pays : United States
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