Evidence map›Paper›PMID 31745220›Full record

ArticleThe pharmacogenomics journal2020

Gender based differences, pharmacogenetics and adverse events in chronic pain management.

Beatriz Planelles, César Margarit, María-Del-Mar Inda, Pura Ballester, Javier Muriel, Jordi Barrachina, Raquel Ajo, María-Dolores Esteban, Ana M Peiró

Abstract read
PubMed Publisher
In one paragraph

Article in The pharmacogenomics journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Observational
  18. Article
  19. Article
  20. Article
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

9 authors at 2 institutions in 1 country.

Beatriz PlanellesPain Unit, Department of Health, Alicante General Hospital, Alicante, Spain.
César MargaritPain Unit, Department of Health, Alicante General Hospital, Alicante, Spain.
María-Del-Mar IndaNeuropharmacology apply to Pain and Functional Diversity (NED). ISABIAL-FISABIO Foundation, General University Hospital of Alicante, Alicante, Spain.
Pura BallesterNeuropharmacology apply to Pain and Functional Diversity (NED). ISABIAL-FISABIO Foundation, General University Hospital of Alicante, Alicante, Spain.
Javier MurielNeuropharmacology apply to Pain and Functional Diversity (NED). ISABIAL-FISABIO Foundation, General University Hospital of Alicante, Alicante, Spain.
Jordi BarrachinaOccupational Observatory, Miguel Hernandez University, Elche, Spain.
Raquel AjoNeuropharmacology apply to Pain and Functional Diversity (NED). ISABIAL-FISABIO Foundation, General University Hospital of Alicante, Alicante, Spain.
María-Dolores EstebanCenter of Operations Research, Miguel Hernandez University, Elche, Spain.
Ana M PeiróPain Unit, Department of Health, Alicante General Hospital, Alicante, Spain. peiro_ana@gva.es.ORCID http://orcid.org/0000-0002-2385-3749
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana · ESUniversitat de Miguel Hernández d'Elx · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Safety data in chronic non-cancer pain (CNCP) with long-term opioid therapy has been poorly studied and can be differently influenced by gender. Furthermore, pharmacogenetics (PGx) could possibly be used to tailor pain medication based on the individual's genetic background. The aim was to assess whether PGx applied to a pharmacovigilance system could help to improve a patient's security profile. A pharmacovigilance data recording system was conducted over 24 months, including genotyping of OPRM1 variants (opioid receptor, A118G) and COMT (enzyme that degrades catecholamines such as norepinephrine, G1947A). Pain intensity (visual analogue scale, VAS), morphine equivalent daily dose (MEDD), adverse events (AEs) and suspected adverse drug reactions (ADRs) were recorded and analysed by gender. The Ethics Committee approved the study and data were analysed with R 3.6.0 software. A total of 748 patients were recruited in the study (67% female, VAS 62 ± 29 mm, MEDD 119 ± 114 mg/day) reporting a median of 6 (3.5-9) AEs/patient. Women presented more nausea, headaches, insomnia, loss of appetite, weight change, depression and dizziness than men. Analysis by genotype demonstrated that PGx influenced the prevalence of vomiting and depression in men, dizziness in women and sexual dysfunction in both. Physicians notified 150 ADRs mostly in females (79%) related to nervous system disorders. PGx applied to a pharmacovigilance recording system provides important information to achieve a better knowledge about AEs in CNCP pharmacological therapy. OPRM1 and COMT polymorphisms were associated with AEs in CNCP patients that differed according to gender.

Indexed as

Sex CharacteristicsAgedAged, 80 and overAnalgesics, OpioidChronic PainDrug-Related Side Effects and Adverse ReactionsFemaleHumansMaleMiddle AgedPain ManagementPain MeasurementPharmacogeneticsPolymorphism, Single NucleotideSpainAnalgesics, Opioid

Identifiers

PMID31745220
OpenAlexW2990975953

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.