Vasopressin SNP pain factors and stress in sickle cell disease

Autor: Marie L. Suarez, Robert E. Molokie, Zaijie Jim Wang, Yingwei Yao, Keesha L. Powell-Roach, Miriam O. Ezenwa, Diana J. Wilkie, Ying He, Ellie H. Jhun
Jazyk: angličtina
Rok vydání: 2019
Předmět:
Male
Critical Care and Emergency Medicine
Peptide Hormones
Social Sciences
Disease
Biochemistry
0302 clinical medicine
Acute care
Genotype
Outpatients
Medicine and Health Sciences
Medicine
Psychology
Ethnicities
Stress measures
Amino Acids
African American people
Multidisciplinary
Organic Compounds
Chronic pain
Hematology
Population groupings
Middle Aged
3. Good health
Chemistry
Genetic Diseases
030220 oncology & carcinogenesis
Physical Sciences
Female
Basic Amino Acids
Vasopressin
Research Article
Adult
medicine.medical_specialty
Patients
Vasopressins
Science
Psychological Stress
Pain
Single-nucleotide polymorphism
Anemia
Sickle Cell

Arginine
Polymorphism
Single Nucleotide

Molecular Genetics
03 medical and health sciences
Young Adult
Autosomal Recessive Diseases
Internal medicine
Mental Health and Psychiatry
Genetics
SNP
Humans
Genetic Predisposition to Disease
Molecular Biology
Aged
Clinical Genetics
Sickle Cell Disease
business.industry
Organic Chemistry
Chemical Compounds
Biology and Life Sciences
Proteins
medicine.disease
Hormones
Genotype frequency
Health Care
Hemoglobinopathies
People and places
business
030217 neurology & neurosurgery
Stress
Psychological
Zdroj: PLoS ONE
PLoS ONE, Vol 14, Iss 11, p e0224886 (2019)
ISSN: 1932-6203
Popis: PurposeFrequencies of single nucleotide polymorphisms (SNPs) from pain related candidate genes are available for individuals with sickle cell disease (SCD). One of those genes, the arginine vasopressin receptor 1A gene (AVPR1A) and one of its SNPs, rs10877969, has been associated with pain and disability in other pain populations. In patients with SCD, clinical factors such as pain and stress have been associated with increased health care utilization, but it is not known if the presence of the AVPR1A SNP plays a role in this observation. The study purpose was to explore the relationships between rs10877969 and self-reported pain, stress, and acute care utilization events among individuals with SCD.MethodsIn a cross-sectional investigation of outpatients with SCD, participants completed PAINReportIt®, a computerized pain measure, to describe their pain experience and contributed blood or saliva samples for genetic analysis. We extracted emergency department and acute care utilization from medical records.ResultsThe SNP genotype frequencies (%) for this sample were CC 30 (28%), CT 44 (41%), TT 33 (31%). Acute care utilization and stress as an aggravator of pain were significantly associated with the rs10877969 genotype (p = .02 and p = .002, respectively). The CT genotype had the highest mean utilization and CC genotype was associated with not citing stress as a pain aggravator. Chronic pain was not associated with rs10877969 (p = .41).ConclusionThis study shows that rs10877969 is related to indicators of stress and acute pain. Further research is recommended with other measures of stress and acute pain.
Databáze: OpenAIRE
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