Publications by authors named "Geetika Narang"

Purpose: Primaquine (PQ) is recommended for radical cure of Plasmodium vivax (Pv) malaria, but its utilization is still limited due to high risk of severe haemolytic anaemia in patients with glucose-6-phosphate dehydrogenase deficiency (G6PD-d). The aim of the present study is to assess the different genotypic variants leading to G6PD-d in Delhi and Goa regions of India.

Methods: A total of 46 samples (34 retrospective Pv-mono-infected samples and 12 Pv-uninfected samples) were included in the study.

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Unlabelled: The high genetic diversity of () is a big obstacle to successful vaccine development programs. Here, the geographical and temporal dynamics of the genetic diversity of Indian isolates from patients living in Ranchi, Raipur, Mewat, and Rourkela were analyzed. Typing and frequency of merozoite surface protein 1 and 2 genes (), their genotypes, clonality, heterozygosity, multiplicity of infection, and neutral evolution metrics were computed.

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Unlabelled: This study analysed the genetic diversity of DBL1α domain of gene in severe and non-severe malaria patients from Delhi and Mewat in Northern India. After confirming infection, samples were cloned and the gene DBL1α domain was sequenced. Out of 377 cloned DBL sequences, 194 were from severe samples and 183 from non-severe samples.

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The bulk of malaria rapid diagnostic tests (RDTs) target histidine-rich protein 2 of Plasmodium falciparum, the deadliest malaria species. The WHO considers pfhrp2/3 deletions as one of the main threats to successful malaria control and/or elimination; as such, parasites that lack part or all of the pfhrp2 gene are missed by pfHRP2-targeting RDTs. Such deletions have been reported in several African and Asian countries, but little is known in Cameroon and India.

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Article Synopsis
  • The study focuses on the challenge of antimalarial drug resistance in malaria-causing parasites P. falciparum (Pf) and P. vivax (Pv), analyzing mutations in five key drug resistance genes from 342 field isolates collected between 1993 and 2014.
  • Significant mutations linked to drug resistance were found in both Pf and Pv, particularly for chloroquine (CQ) and sulfadoxine-pyrimethamine (SP), while no mutations related to artemisinin (ART) resistance were observed.
  • The research highlights the need for ongoing monitoring of drug resistance mutations to effectively control and eliminate malaria, emphasizing the genetic variations that affect treatment efficacy.
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Background: This review presents an overview of field findings on sequence variation of histidine-rich proteins 2/3 (HRP2/3) for which reference types (1-24) have been identified, and its critical impact on HRP2-based rapid diagnostic test (RDT) detection.

Research Design And Methods: This systematic review and meta-analysis was registered with PROSPERO, CRD42022316027, and conducted as per the PRISMA guidelines, and the methodological quality of studies was assessed.

Results: Of the 2184 records identified, 34 studies were included mostly from Africa (47.

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Background: Drug resistance is a serious impediment to efficient control and elimination of malaria in endemic areas.

Methods: This study aimed at analysing the genetic profile of molecular drug resistance in Plasmodium falciparum and Plasmodium vivax parasites from India over a ~ 30-year period (1993-2019). Blood samples of P.

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Globally, malaria is a public health concern, with severe malaria (SM) contributing a major share of the disease burden in malaria endemic countries. In this context, identification and validation of SM biomarkers are essential in clinical practice. Some biomarkers (C-reactive protein, angiopoietin 2, angiopoietin-2/1 ratio, platelet count, histidine-rich protein 2) have yielded interesting results in the prognosis of severe malaria, but for severe and malaria, similar evidence is missing.

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