Cargando…

Association of genetic variation in COMT gene with pain related to sickle cell disease in patients from the walk-PHaSST study

BACKGROUND: Vaso-occlusive pain episodes (VOEs) are the hallmark of sickle cell disease (SCD), and our current understanding of disease biology, treatment, and psychological covariates does not adequately explain the variability of pain in SCD. Functional variants in catechol-O-methyltransferase (CO...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhang, Yingze, Belfer, Inna, Nouraie, Mehdi, Zeng, Qilu, Goel, Ruchika, Chu, Yanxia, Krasiy, Inna, Krishnamurti, Lakshmanan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Dove Medical Press 2018
Materias:	Original Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856032/ https://www.ncbi.nlm.nih.gov/pubmed/29559808 http://dx.doi.org/10.2147/JPR.S149958

Ejemplares similares

Pain catastrophizing is associated with poorer health-related quality of life in pediatric patients with sickle cell disease
por: Bakshi, Nitya, et al.
Publicado: (2018)

Quantitative sensory testing is feasible and is well-tolerated in patients with sickle cell disease following a vaso-occlusive episode
por: Bakshi, Nitya, et al.
Publicado: (2018)

Hematopoietic Cell Transplantation for Sickle Cell Disease
por: Krishnamurti, Lakshmanan
Publicado: (2021)

Acute Chest Syndrome in Children with Sickle Cell Disease
por: Jain, Shilpa, et al.
Publicado: (2017)

Assessing Patient Preferences for Treatment Options for Pediatric Sickle Cell Disease: A Critical Review of Quantitative and Qualitative Studies
por: Katoch, Deeksha, et al.
Publicado: (2021)

Nature and Nurture of Human Pain
por: Belfer, Inna
Publicado: (2013)

Sex-Specific Genetic Control of Diabetic Neuropathic Pain Suggests Subsequent Development of Men-only and Women—Only Analgesic Strategies
por: Belfer, Inna
Publicado: (2015)

Presence of pain on three or more days of the week is associated with worse patient reported outcomes in adults with sickle cell disease
por: Bakshi, Nitya, et al.
Publicado: (2018)

Thrombo-Inflammation in COVID-19 and Sickle Cell Disease: Two Faces of the Same Coin
por: Chiang, Kate Chander, et al.
Publicado: (2023)

Intraindividual pain variability and phenotypes of pain in sickle cell disease: a secondary analysis from the Pain in Sickle Cell Epidemiology Study
por: Bakshi, Nitya, et al.
Publicado: (2022)

Management of Chronic Pain in Adults Living With Sickle Cell Disease in the Era of the Opioid Epidemic: A Qualitative Study
por: Sinha, Cynthia B., et al.
Publicado: (2019)

Hydroxyurea therapy for children with sickle cell disease: describing how caregivers make this decision
por: Creary, Susan, et al.
Publicado: (2015)

From trust to skepticism: An in-depth analysis across age groups of adults with sickle cell disease on their perspectives regarding hydroxyurea
por: Sinha, Cynthia B., et al.
Publicado: (2018)

Primary caregiver decision-making in hematopoietic cell transplantation and gene therapy for sickle cell disease
por: Sinha, Cynthia B., et al.
Publicado: (2020)

Prevalence and predictors of chronic pain intensity and disability among adults with sickle cell disease
por: Matthie, Nadine, et al.
Publicado: (2020)

Proponent or collaborative: Physician perspectives and approaches to disease modifying therapies in sickle cell disease
por: Bakshi, Nitya, et al.
Publicado: (2017)

Metabolic correlates to critical speed in murine models of sickle cell disease
por: Cendali, Francesca I., et al.
Publicado: (2023)

Comte
por: Marvin, Francis Sydney, 1863-1943
Publicado: (1941)

Improving PHA production in a SBR of coupling PHA-storing microorganism enrichment and PHA accumulation by feed-on-demand control
por: Zeng, Shanwen, et al.
Publicado: (2018)

Structural Insights on PHA Binding Protein PhaP from Aeromonas hydrophila
por: Zhao, Hongyu, et al.
Publicado: (2016)

PHA Production and PHA Synthases of the Halophilic Bacterium Halomonas sp. SF2003
por: Thomas, Tatiana, et al.
Publicado: (2020)

A Decision Support Tool for Allogeneic Hematopoietic Stem Cell Transplantation for Children With Sickle Cell Disease: Acceptability and Usability Study
por: Veludhandi, Anirudh, et al.
Publicado: (2021)

Radiological protection in SST aircraft
por: Fuller, E W, et al.
Publicado: (1971)

Association of COMT and COMT-DRD2 interaction with creative potential
por: Zhang, Shun, et al.
Publicado: (2014)

Serum albumin is independently associated with higher mortality in adult sickle cell patients: Results of three independent cohorts
por: Nouraie, Mehdi, et al.
Publicado: (2020)

Role of PhaC Type I and Type II Enzymes during PHA Biosynthesis
por: Mezzolla, Valeria, et al.
Publicado: (2018)

Voltage-gated Na(+) currents in human dorsal root ganglion neurons
por: Zhang, Xiulin, et al.
Publicado: (2017)

Patient and family experience with chronic transfusion therapy for sickle cell disease: A qualitative study
por: Hawkins, Lauren M., et al.
Publicado: (2020)

Advances in Polyhydroxyalkanoate (PHA) Production
por: Koller, Martin
Publicado: (2017)

Polyhydroxyalkanoates (PHA) genes Database
por: Alamgeer, Mohammad
Publicado: (2019)

Influence of growth stage on activities of polyhydroxyalkanoate (PHA) polymerase and PHA depolymerase in Pseudomonas putida U
por: Ren, Qun, et al.
Publicado: (2010)

Assessment of Patient and Caregiver Attitudes and Approaches to Decision-Making Regarding Bone Marrow Transplant for Sickle Cell Disease: A Qualitative Study
por: Bakshi, Nitya, et al.
Publicado: (2020)

Sociologie de Comte
por: Arnaud, Pierre
Publicado: (1969)

Sociología de Comte
por: Arnaud, Pierre
Publicado: (1971)

Pannenserie l sst Kosten explodieren
Publicado: (2009)

The PHA Depolymerase Engineering Database: A systematic analysis tool for the diverse family of polyhydroxyalkanoate (PHA) depolymerases
por: Knoll, Michael, et al.
Publicado: (2009)

The NPR1 ortholog PhaNPR1 is required for the induction of PhaPR1 in Phalaenopsis aphrodite
por: Chen, Jen-Chih, et al.
Publicado: (2013)

Sex and frequency of pain episodes are associated with acute pain trajectories in adolescents with sickle cell disease
por: Astles, Rachel, et al.
Publicado: (2023)

Metabolic signatures of cardiorenal dysfunction in plasma from sickle cell patients as a function of therapeutic transfusion and hydroxyurea treatment
por: D’Alessandro, Angelo, et al.
Publicado: (2023)

Risk Factors for Death in 632 Patients with Sickle Cell Disease in the United States and United Kingdom
por: Gladwin, Mark T., et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_klusq9dbvf36km7h88ee5cth84