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1.
BMJ Case Rep ; 17(4)2024 Apr 04.
Article in English | MEDLINE | ID: mdl-38575333

ABSTRACT

SummaryHereditary haemorrhagic telangiectasia (HHT) has an estimated prevalence of 1 in 5000-8000 individuals globally with pulmonary arteriovenous malformations (PAVMs) affecting approximately 15%-50% of HHT patients. Ischaemic stroke is a known complication of PAVMs that affects ≤30% of patients with PAVMs. Studies have shown that patients with PAVMs have ischaemic stroke a decade earlier than routine stroke. The predominant mechanism of ischaemic stroke in HHT patients is paradoxical embolism due to PAVMs, but most HHT-related PAVMs are asymptomatic. Additionally, HHT is often underdiagnosed in patients and poses a challenge to physicians due to its rarity. We present a case of a patient with ischaemic stroke who was subsequently diagnosed with HHT and found to have a PAVM on further evaluation. This case highlights the importance of using an individualised patient-centred stroke evaluation and screening for PAVMs in patients who had a stroke with possible or suspected HHT and definite HHT.


Subject(s)
Arteriovenous Fistula , Arteriovenous Malformations , Brain Ischemia , Ischemic Stroke , Pulmonary Artery , Pulmonary Veins , Stroke , Telangiectasia, Hereditary Hemorrhagic , Humans , Arteriovenous Malformations/complications , Arteriovenous Malformations/diagnosis , Brain Ischemia/complications , Hemorrhage/complications , Ischemic Stroke/complications , Pulmonary Artery/diagnostic imaging , Pulmonary Artery/abnormalities , Pulmonary Veins/abnormalities , Stroke/etiology , Stroke/complications , Telangiectasia, Hereditary Hemorrhagic/complications , Telangiectasia, Hereditary Hemorrhagic/diagnosis , Telangiectasia, Hereditary Hemorrhagic/therapy , Female , Middle Aged
2.
medRxiv ; 2024 Feb 13.
Article in English | MEDLINE | ID: mdl-36865135

ABSTRACT

The Zanzibar archipelago of Tanzania has become a low-transmission area for Plasmodium falciparum. Despite being considered an area of pre-elimination for years, achieving elimination has been difficult, likely due to a combination of imported infections from mainland Tanzania, and continued local transmission. To shed light on these sources of transmission, we applied highly multiplexed genotyping utilizing molecular inversion probes to characterize the genetic relatedness of 282 P. falciparum isolates collected across Zanzibar and in Bagamoyo District on the coastal mainland from 2016-2018. Overall, parasite populations on the coastal mainland and Zanzibar archipelago remain highly related. However, parasite isolates from Zanzibar exhibit population microstructure due to rapid decay of parasite relatedness over very short distances. This, along with highly related pairs within shehias, suggests ongoing low level local transmission. We also identified highly related parasites across shehias that reflect human mobility on the main island of Unguja and identified a cluster of highly related parasites, suggestive of an outbreak, in the Micheweni district on Pemba island. Parasites in asymptomatic infections demonstrated higher complexity of infection than those in symptomatic infections, but have similar core genomes. Our data support importation as a main source of genetic diversity and contribution to the parasite population on Zanzibar, but they also show local outbreak clusters where targeted interventions are essential to block local transmission. These results highlight the need for preventive measures against imported malaria and enhanced control measures in areas that remain receptive for malaria reemergence due to susceptible hosts and competent vectors.

3.
PLoS Negl Trop Dis ; 16(7): e0010648, 2022 07.
Article in English | MEDLINE | ID: mdl-35867730

ABSTRACT

Genotyping Plasmodium vivax relapses can provide insights into hypnozoite biology. We performed targeted amplicon sequencing of 127 relapses occurring in Indonesian soldiers returning to malaria-free Java after yearlong deployment in malarious Eastern Indonesia. Hepatic carriage of multiple hypnozoite clones was evident in three-quarters of soldiers with two successive relapses, yet the majority of relapse episodes only displayed one clonal population. The number of clones detected in relapse episodes decreased over time and through successive relapses, especially in individuals who received hypnozoiticidal therapy. Interrogating the multiplicity of infection in this P. vivax relapse cohort reveals evidence of independent activation and slow depletion of hypnozoites over many months by multiple possible mechanisms, including parasite senescence and host immunity.


Subject(s)
Antimalarials , Malaria, Vivax , Malaria , Parasites , Animals , Antimalarials/therapeutic use , Humans , Malaria/parasitology , Malaria, Vivax/parasitology , Plasmodium vivax/genetics , Recurrence
4.
Am J Trop Med Hyg ; 104(4): 1371-1374, 2021 02 08.
Article in English | MEDLINE | ID: mdl-33556035

ABSTRACT

Ultrasensitive PCR used in low-transmission malaria-endemic settings has revealed a much higher burden of asymptomatic infections than that detected by rapid diagnostic tests (RDTs) or standard PCR, but there is limited evidence as to whether this is the case in higher transmission settings. Using dried blood spots (DBS) collected among 319 schoolchildren in Bagamoyo, Tanzania, we found good correlation (Pearson's R = 0.995) between Plasmodium falciparum parasite densities detected by a DNA-based 18s rRNA real-time PCR (qPCR) and an RNA-based ultrasensitive reverse transcriptase (RT)-PCR (usPCR) for the same target. Whereas prevalence by usPCR was higher than that found by qPCR (37% versus 32%), the proportion of additionally detected low-density infections (median parasite density < 0.050 parasites/µL) represented an incremental increase. It remains unclear to what extent these low-density infections may contribute to the infectious reservoir in different malaria transmission settings.


Subject(s)
DNA, Protozoan/genetics , Dried Blood Spot Testing/methods , Malaria, Falciparum/diagnosis , Plasmodium falciparum/genetics , Polymerase Chain Reaction/methods , Polymerase Chain Reaction/standards , Asymptomatic Infections , Child , Cross-Sectional Studies , Dried Blood Spot Testing/standards , Female , Humans , Malaria, Falciparum/epidemiology , Male , Prevalence , RNA, Ribosomal, 18S , Tanzania/epidemiology
5.
Article in English | MEDLINE | ID: mdl-33361308

ABSTRACT

Atovaquone-proguanil remains effective against multidrug-resistant Plasmodium falciparum in Southeast Asia, but resistance is mediated by a single point mutation in cytochrome b (cytb) that can arise during treatment. Among 14 atovaquone-proguanil treatment failures in a clinical trial in Cambodia, only one recrudescence harbored the cytb mutation Y268C. Deep sequencing did not detect the mutation at baseline or in the first 3 days of treatment, suggesting that it arose de novo Further sequencing across cytb similarly found no low-frequency cytb mutations that were up-selected from baseline to recrudescence. Copy number amplification in dihydroorotate dehydrogenase (DHODH) and cytb as markers of atovaquone tolerance was also absent. Cytb mutation played a minor role in atovaquone-proguanil treatment failures in an active comparator clinical trial.


Subject(s)
Antimalarials , Malaria, Falciparum , Naphthoquinones , Antimalarials/therapeutic use , Atovaquone/therapeutic use , Cambodia , Cytochromes b/genetics , Drug Combinations , Humans , Malaria, Falciparum/drug therapy , Naphthoquinones/therapeutic use , Plasmodium falciparum/genetics , Proguanil/therapeutic use
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