Evidence map›Paper›PMID 16103897›Full record

ArticleThe pharmacogenomics journal2005

Clinical response to morphine in cancer patients and genetic variation in candidate genes.

J R Ross, D Rutter, K Welsh, S P Joel, K Goller, A U Wells, R Du Bois, J Riley

3 registry-linked trialsAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in The pharmacogenomics journal, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
9.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01731873 completednot on this mapstarted 2012, after this paper: background citation

Non-Interventional Pharmacogenetic Study of Patient / Proxy Controlled Analgesia in Children Undergoing Surgery

TypeobservationalSponsorChildren's Hospital Medical Center, CincinnatiRan2012 to 2019Enrolled182ConditionsPain
NCT01813695 completednot on this mapstarted 2013, after this paper: background citation

Preemptive Genotyping of Children and Adolescents at Risk for Surgery and Subsequent Pain Management

TypeobservationalSponsorChildren's Hospital Medical Center, CincinnatiRan2013 to 2022Enrolled576ConditionsPainArmsPreemptive genotyping in medical record, Genotyping not included in electronic medical record
NCT01839461 completednot on this mapstarted 2009, after this paper: background citation

Personalizing Perioperative Morphine Analgesia for Adolescents Undergoing Major Spine Surgeries

TypeobservationalSponsorChildren's Hospital Medical Center, CincinnatiRan2009 to 2019Enrolled137ConditionsPain
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 148 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

J R RossDepartment of Clinical Genomics, Imperial College, London, UK. joy.ross@rmhnthames.nhs.uk
D Rutter
K Welsh
S P Joel
K Goller
A U Wells
R Du Bois
J Riley
Royal Marsden Hospital · GBGenomics England · GBSt Bartholomew's Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Morphine is the analgesic of choice for moderate to severe cancer pain; however, 10-30% of patients do not tolerate morphine. This study evaluated genetic variation in the mu-opioid receptor, betaarrestin2, stat6 and uridine diphosphate-glucuronysltransferase 2B7 (UGT2B7) genes, in patients who responded to morphine vs those who were switched to alternative opioids. We prospectively recruited and genotyped 162 Caucasian patients (117 controls, 39 switchers). Switchers, were more likely to carry the common allele at 1182 G/A, 5864 G/A, 8622T/C and 11143 G/A in the betaarrestin2 gene (P = 0.021, 0.043, 0.013, 0.043, respectively). Switchers had increased carriage of the T allele (-1714 C/T) and a significant difference in the allelic frequency at 9065 C/T (chi(2) = 3.86, P = 0.049) in the stat6 gene. No differences were seen in genotype or allele frequencies of SNPs in the mu-opioid receptor gene or UGT2B7 gene. This study presents novel data suggesting that variation in genes involved in mu-opioid receptor signalling influence clinical response to morphine.

Indexed as

AllelesAnalgesics, OpioidArrestinsbeta-ArrestinsConfusionFemaleGene FrequencyGlucuronosyltransferaseHaplotypesHumansIntractable PainMaleMiddle AgedMorphineNauseaNeoplasmsAnalgesics, OpioidArrestinsbeta-ArrestinsGlucuronosyltransferaseMorphineReceptors, Opioid, muUGT2B7 protein, human

Identifiers

PMID16103897
OpenAlexW2066501217

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.