Evidence map›Paper›PMID 34407160›Full record

ArticleRevista do Instituto de Medicina Tropical de Sao Paulo2021

Surveillance of molecular markers of antimalarial drug resistance in Plasmodium falciparum and Plasmodium vivax in Federally Administered Tribal Area (FATA), Pakistan.

Muhammad Faisal Nadeem, Aamer Ali Khattak, Nadia Zeeshan, Hamza Zahid, Usman Ayub Awan, Adnan Yaqoob, Naeem Mahmood Ashraf, Sana Gul, Sadia Alam, Waqas Ahmed

Abstract read
In one paragraph

Article in Revista do Instituto de Medicina Tropical de Sao Paulo, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Genetic Diversity ofTropical medicine and infectious disease · 2023
    Article
  3. PvMSP-3α and PvMSP-3β genotyping reveals higher genetic diversity in Plasmodium vivax parasites from migrant workers than residents at the China-Myanmar border.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2022
    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

10 authors.

Muhammad Faisal NadeemUniversity of Gujrat, Department of Biochemistry & Biotechnology, Gujrat, Punjab, Pakistan.
Aamer Ali KhattakThe University of Haripur, Department of Medical Laboratory Technology, Haripur, Khyber Pakhtunkhwa, Pakistan.ORCID http://orcid.org/0000-0002-9400-2984
Nadia ZeeshanUniversity of Gujrat, Department of Biochemistry & Biotechnology, Gujrat, Punjab, Pakistan.
Hamza ZahidSandeman Provincial Hospital, Department of Surgery, Quetta, Balochistan, Pakistan.
Usman Ayub AwanThe University of Haripur, Department of Medical Laboratory Technology, Haripur, Khyber Pakhtunkhwa, Pakistan.ORCID http://orcid.org/0000-0003-1183-2788
Adnan YaqoobUniversity of Gujrat, Department of Biochemistry & Biotechnology, Gujrat, Punjab, Pakistan.
Naeem Mahmood AshrafUniversity of Gujrat, Department of Biochemistry & Biotechnology, Gujrat, Punjab, Pakistan.
Sana GulNational University of Medical Sciences, Department of Biological Sciences, Rawalpindi, Pujab, Pakistan.
Sadia AlamThe University of Haripur, Department of Microbiology, Haripur, Khyber Pakhtunkhwa, Pakistan.
Waqas AhmedThe University of Haripur, Department of Microbiology, Haripur, Khyber Pakhtunkhwa, Pakistan.ORCID http://orcid.org/0000-0001-7744-3916

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This molecular epidemiological study was designed to determine the antimalarial drug resistance pattern, and the genetic diversity of malaria isolates collected from a war-altered Federally Administered Tribal Area (FATA), in Pakistan. Clinical isolates were collected from Bajaur, Mohmand, Khyber, Orakzai and Kurram agencies of FATA region between May 2017 and May 2018, and they underwent DNA extraction and amplification. The investigation of gene polymorphisms in drug resistance genes (dhfr, dhps, crt, and mdr1) of Plasmodium falciparum and Plasmodium vivax was carried out by pyrosequencing and Sanger sequencing, respectively. Out of 679 PCR-confirmed malaria samples, 523 (77%) were P. vivax, 121 (18%) P. falciparum, and 35 (5%) had mixed-species infections. All P. falciparum isolates had pfdhfr double mutants (C59R+S108N), while pfdhfr/pfdhps triple mutants (C59R+S108N+A437G) were detected in 11.5% of the samples. About 97.4% of P. falciparum isolates contained pfcrt K76T mutation, while pfmdr1 N86Y and Y184F mutations were present in 18.2% and 10.2% of the samples. P. vivax pvdhfr S58R mutation was present in 24.9% of isolates and the S117N mutation in 36.2%, while no mutation in the pvdhps gene was found. Pvmdr1 F1076L mutation was found in nearly all samples, as it was observed in 98.9% of isolates. No significant anti-folate and chloroquine resistance was observed in P. vivax; however, mutations associated with antifolate-resistance were found, and the chloroquine-resistant gene has been observed in 100% of P. falciparum isolates. Chloroquine and sulphadoxine-pyrimethamine resistance were found to be high in P. falciparum and low in P. vivax. Chloroquine could still be used for P. vivax infection but need to be tested in vivo, whereas a replacement of the artemisinin combination therapy for P. falciparum appears to be justified.

Indexed as

AntimalarialsMalaria, FalciparumDrug ResistanceHumansMutationPakistanPlasmodium falciparumPlasmodium vivaxProtozoan ProteinsAntimalarialsProtozoan Proteins

Identifiers

PMID34407160
PMCPMC8323834

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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.