chronic pain |
Disease ID | 696 |
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Disease | chronic pain |
Manually Symptom | UMLS | Name(Total Manually Symptoms:50) C2364108 | stigma C2364074 | drug abuse C2364072 | depression C2364051 | fatigue C2364045 | activity intolerance C1963237 | insomnia C1963138 | hypertension C1963087 | constipation C1963064 | anxiety C1842981 | neuroticism C1839611 | n syndrome C1660219 | analgesia C1568272 | tendinopathy C1546654 | granuloma C1269683 | major depressive disorder C1269683 | major depression C1135120 | breakthrough pain C0947622 | gallstones C0853946 | exacerbation of pain C0851578 | sleep problem C0851578 | sleep disturbances C0851578 | sleep disorders C0751188 | postdural puncture headache C0700361 | distress C0700201 | sleep disturbance C0679466 | cognitive deficits C0575031 | cervical facet joint pain C0549622 | sexual dysfunction C0522224 | palsy C0520680 | central sleep apnea C0278139 | moderate pain C0269106 | endosalpingiosis C0262471 | ent problem C0262405 | brain dysfunction C0240735 | personality changes C0233470 | constricted affect C0086439 | reduced activity C0086132 | emotional depression C0086132 | depressive symptoms C0038436 | posttraumatic stress disorder C0038436 | post-traumatic stress disorder C0038220 | status epilepticus C0037650 | somatoform disorders C0031212 | personality disorders C0029095 | opioid abuse C0020604 | hypochondriasis C0004936 | mental disorders C0003469 | anxiety disorders C0002962 | angina pectoris C0002020 | alexithymia |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:30) C0011570 | depression | 54 C0003467 | anxiety | 29 C0231303 | distress | 19 C0002766 | analgesia | 11 C0917801 | insomnia | 11 C0015672 | fatigue | 7 C0086132 | depressive symptoms | 6 C0037317 | sleep disturbance | 6 C1839611 | n syndrome | 4 C0041696 | major depressive disorder | 4 C0009806 | constipation | 4 C0033953 | sexual dysfunction | 3 C0041696 | major depression | 2 C0031212 | personality disorders | 2 C0002020 | alexithymia | 2 C0003469 | anxiety disorders | 2 C0700201 | sleep problem | 2 C0851578 | sleep disorders | 2 C1135120 | breakthrough pain | 1 C0037317 | sleep disturbances | 1 C0853946 | exacerbation of pain | 1 C0020538 | hypertension | 1 C0037650 | somatoform disorders | 1 C0013146 | drug abuse | 1 C0004936 | mental disorders | 1 C0038436 | post-traumatic stress disorder | 1 C0679466 | cognitive deficits | 1 C0029095 | opioid abuse | 1 C0520680 | central sleep apnea | 1 C0522224 | palsy | 1 |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
All Snps(Total Genotypes:9) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs1045642 | 23803057 | 4988 | OPRM1 | umls:C0150055 | BeFree | Polymorphisms of OPRM1 A118G and ABCB1 C3435T have been suggested to contribute to inter-individual variability regarding pain sensitivity, opioid usage, tolerance and dependence and incidence of adverse effects in patients with chronic pain. | 0.001357209 | 2015 | ABCB1 | 7 | 87509329 | A | T,G |
rs1045642 | 23803057 | 5243 | ABCB1 | umls:C0150055 | BeFree | Polymorphisms of OPRM1 A118G and ABCB1 C3435T have been suggested to contribute to inter-individual variability regarding pain sensitivity, opioid usage, tolerance and dependence and incidence of adverse effects in patients with chronic pain. | 0.000542884 | 2015 | ABCB1 | 7 | 87509329 | A | T,G |
rs1799971 | 23803057 | 4988 | OPRM1 | umls:C0150055 | BeFree | Polymorphisms of OPRM1 A118G and ABCB1 C3435T have been suggested to contribute to inter-individual variability regarding pain sensitivity, opioid usage, tolerance and dependence and incidence of adverse effects in patients with chronic pain. | 0.001357209 | 2015 | OPRM1 | 6 | 154039662 | A | G |
rs1799971 | 17000822 | 4988 | OPRM1 | umls:C0150055 | BeFree | A genetic association study of the functional A118G polymorphism of the human mu-opioid receptor gene in patients with acute and chronic pain. | 0.001357209 | 2006 | OPRM1 | 6 | 154039662 | A | G |
rs1799971 | 23803057 | 5243 | ABCB1 | umls:C0150055 | BeFree | Polymorphisms of OPRM1 A118G and ABCB1 C3435T have been suggested to contribute to inter-individual variability regarding pain sensitivity, opioid usage, tolerance and dependence and incidence of adverse effects in patients with chronic pain. | 0.000542884 | 2015 | OPRM1 | 6 | 154039662 | A | G |
rs386602118 | 21049025 | 1312 | COMT | umls:C0150055 | BeFree | However, genetic effects (COMT Val(158)Met and BDNF Val(66)Met) on experimental pain were moderated by the presence of chronic pain. | 0.002171535 | 2010 | NA | NA | NA | NA | NA |
rs4680 | 22722321 | 1312 | COMT | umls:C0150055 | BeFree | The meta-analyses showed that fibromyalgia or chronic widespread pain is the only type of chronic pain that could be associated with the COMT single nucleotide polymorphism rs4680 (Val158Met). | 0.002171535 | 2012 | COMT;MIR4761 | 22 | 19963748 | G | A |
rs4680 | 21049025 | 1312 | COMT | umls:C0150055 | BeFree | However, genetic effects (COMT Val(158)Met and BDNF Val(66)Met) on experimental pain were moderated by the presence of chronic pain. | 0.002171535 | 2010 | COMT;MIR4761 | 22 | 19963748 | G | A |
rs4680 | 23773341 | 1312 | COMT | umls:C0150055 | BeFree | This study highlights the importance of COMT rs4680 in influencing the clinical response to drugs used for chronic pain, including opioid analgesics and triptans. | 0.002171535 | 2013 | COMT;MIR4761 | 22 | 19963748 | G | A |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Chemical(Total Drugs:1) | |||||||||
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CUI | ChemicalName | ChemicalID | CasRN | DiseaseName | DiseaseID | DirectEvidence | PubMedIDs | ||
C0150055 | pregabalin | D000069583 | - | chronic pain | MESH:D059350 | therapeutic | 19664204 |
FDA approved drug and dosage information(Total Drugs:3) | ||||||||
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DiseaseID | Drug_name | active_ingredients | strength | Dosage Form/Route | Marketing Status | TE code | RLD | RS |
MESH:D059350 | lyrica | pregabalin | 25MG | CAPSULE;ORAL | Prescription | None | Yes | No |
MESH:D059350 | lyrica | pregabalin | 25MG | CAPSULE; ORAL | Prescription | None | No | No |
MESH:D059350 | lyrica | pregabalin | 25MG | CAPSULE; ORAL | Prescription | None | No | No |
FDA labeling changes(Total Drugs:3) | |||||||||||||
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DiseaseID | Pediatric_Labeling_Date | Trade_Name | Generic_Name_or_Proper_Name | Indications Studied | Label Changes Summary | Product Labeling | BPCA(B) | PREA(P) | BPCA(B) and PREA(P) | Pediatric Rule (R) | Sponsor | Pediatric Exclusivity Granted Date | NNPS |
MESH:D059350 | 12/22/2016 | lyrica | pregabalin | Fibromyalgia | Safety and efficacy in pediatric patients have not been established. A 15-week, placebo-controlled trial was conducted with 107 pediatric patients with fibromyalgia, ages 12 through 17 years . The primary efficacy endpoint of change from baseline to Week 15 in mean pain intensity showed numerically greater improvement for the pregabalin-treated patients compared to placebo-treated patients, but did not reach statistical significance. The most frequently observed adverse reactions in the clinical trial included dizziness, nausea, headache, weight increased, and fatigue. The overall safety profile in adolescents was similar to that observed in adults with fibromyalgia. Postmarketing study. | Labeling | - | P | - | - | PF Prism CV | - | FALSE |
MESH:D059350 | 12/22/2016 | lyrica | pregabalin | Fibromyalgia | Safety and efficacy in pediatric patients have not been established. A 15-week, placebo-controlled trial was conducted with 107 pediatric patients with fibromyalgia, ages 12 through 17 years . The primary efficacy endpoint of change from baseline to Week 15 in mean pain intensity showed numerically greater improvement for the pregabalin-treated patients compared to placebo-treated patients, but did not reach statistical significance. The most frequently observed adverse reactions in the clinical trial included dizziness, nausea, headache, weight increased, and fatigue. The overall safety profile in adolescents was similar to that observed in adults with fibromyalgia. Postmarketing study. | Labeling | - | P | - | - | PF Prism CV | - | FALSE |
MESH:D059350 | 12/22/2016 | lyrica | pregabalin | Fibromyalgia | Safety and efficacy in pediatric patients have not been established. A 15-week, placebo-controlled trial was conducted with 107 pediatric patients with fibromyalgia, ages 12 through 17 years . The primary efficacy endpoint of change from baseline to Week 15 in mean pain intensity showed numerically greater improvement for the pregabalin-treated patients compared to placebo-treated patients, but did not reach statistical significance. The most frequently observed adverse reactions in the clinical trial included dizziness, nausea, headache, weight increased, and fatigue. The overall safety profile in adolescents was similar to that observed in adults with fibromyalgia. Postmarketing study. | Labeling | - | P | - | - | PF Prism CV | - | FALSE |