Evidence map›Paper›PMID 30706164›Full record

Trial reportParasitology research2019

Effects of MAO-A and CYP450 on primaquine metabolism in healthy volunteers.

Norliza Mat Ariffin, Farida Islahudin, Endang Kumolosasi, Mohd Makmor-Bakry

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Parasitology research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. The Impact ofJournal of personalized medicine · 2024
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Pharmacogenomics · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Frontiers in pharmacology · 2021
    Article
  16. Review
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

4 authors at 1 institution in 1 country.

Norliza Mat AriffinFaculty of Pharmacy, Jalan Raja Muda Abdul Aziz, Abdul Aziz, 50300, Kuala Lumpur, Malaysia.
Farida IslahudinFaculty of Pharmacy, Jalan Raja Muda Abdul Aziz, Abdul Aziz, 50300, Kuala Lumpur, Malaysia. faridaislahudin@yahoo.com.
Endang KumolosasiFaculty of Pharmacy, Jalan Raja Muda Abdul Aziz, Abdul Aziz, 50300, Kuala Lumpur, Malaysia.
Mohd Makmor-BakryFaculty of Pharmacy, Jalan Raja Muda Abdul Aziz, Abdul Aziz, 50300, Kuala Lumpur, Malaysia.
King Abdul Aziz University Hospital · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eliminating the Plasmodium vivax malaria parasite infection remains challenging. One of the main problems is its capacity to form hypnozoites that potentially lead to recurrent infections. At present, primaquine is the only drug used for the management of hypnozoites. However, the effects of primaquine may differ from one individual to another. The aim of this work is to determine new measures to reduce P. vivax recurrence, through primaquine metabolism and host genetics. A genetic study of MAO-A, CYP2D6, CYP1A2 and CYP2C19 and their roles in primaquine metabolism was undertaken of healthy volunteers (n = 53). The elimination rate constant (K

Indexed as

AdultAllelesAntimalarialsCytochrome P-450 Enzyme SystemFemaleGene Expression Regulation, EnzymologicHaplotypesHealthy VolunteersHumansMaleMonoamine OxidasePolymorphism, GeneticPrimaquineRecurrenceAntimalarialsCytochrome P-450 Enzyme SystemMonoamine Oxidasemonoamine oxidase A, humanPrimaquineMalariaPlasmodium vivaxPolymorphismPrimaquine

Identifiers

PMID30706164
OpenAlexW2912579440

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.