Publications by authors named "Deepti Gurdasani"

Background: Limited data exists regarding long Covid burden following Omicron infection in highly vaccinated populations.

Objective: To (1) characterise long Covid prevalence and predictors and (2) identify key symptom clusters and their correlates among long Covid patients, during an Omicron-predominant period in a highly vaccinated population.

Design: Anonymous, online, cross-sectional survey.

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Epidemic surveillance using traditional approaches is dependent on case ascertainment and is delayed. Open-source intelligence (OSINT)-based syndromic surveillance can overcome limitations of delayed surveillance and poor case ascertainment, providing early warnings to guide outbreak response. It can identify outbreaks of unknown cause for which no other global surveillance exists.

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Background: The cause of acute paediatric hepatitis of unknown aetiology (2022) has not been established despite extensive investigation.

Objective: To summarise the evidence for and against a causal role for human adenovirus (HAdv), adeno-associated virus 2 (AAV-2) and SARS-CoV-2 in outbreaks of paediatric hepatitis in 2022.

Methods: We appraised and summarised relevant evidence for each of the Bradford Hill criteria for causality using quantitative (statistical modelling) and qualitative (narrative coherence) approaches.

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Article Synopsis
  • Researchers studied how genetic variation affects vaccine responses in infants from African countries, finding specific HLA associations with antibody responses to vaccines like pertussis and hepatitis B.
  • They used genetic data from over 1,700 individuals to identify patterns in HLA types that could explain up to 10% of the response variability in infants to these vaccines.
  • The study highlighted differences in immune responses based on ancestry, indicating that understanding HLA-DRB1 expression could help refine vaccine design for better effectiveness in diverse populations.
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Mapping the functional human genome and impact of genetic variants is often limited to European-descendent population samples. To aid in overcoming this limitation, we measured gene expression using RNA sequencing in lymphoblastoid cell lines (LCLs) from 599 individuals from six African populations to identify novel transcripts including those not represented in the hg38 reference genome. We used whole genomes from the 1000 Genomes Project and 164 Maasai individuals to identify 8,881 expression and 6,949 splicing quantitative trait loci (eQTLs/sQTLs), and 2,611 structural variants associated with gene expression (SV-eQTLs).

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HIV-1 remains a global health crisis, highlighting the need to identify new targets for therapies. Here, given the disproportionate HIV-1 burden and marked human genome diversity in Africa, we assessed the genetic determinants of control of set-point viral load in 3,879 people of African ancestries living with HIV-1 participating in the international collaboration for the genomics of HIV. We identify a previously undescribed association signal on chromosome 1 where the peak variant associates with an approximately 0.

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Objective: To describe hospital admissions associated with SARS-CoV-2 infection in children and adolescents.

Design: Cohort study of 3.2 million first ascertained SARS-CoV-2 infections using electronic health care record data.

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Vast quantities of open-source data from news reports, social media and other sources can be harnessed using artificial intelligence and machine learning, and utilised to generate valid early warning signals of emerging epidemics. Early warning signals from open-source data are not a replacement for traditional, validated disease surveillance, but provide a trigger for earlier investigation and diagnostics. This may yield earlier pathogen characterisation and genomic data, which can enable earlier vaccine development or deployment of vaccines.

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The use of artificial intelligence (AI) to generate automated early warnings in epidemic surveillance by harnessing vast open-source data with minimal human intervention has the potential to be both revolutionary and highly sustainable. AI can overcome the challenges faced by weak health systems by detecting epidemic signals much earlier than traditional surveillance. AI-based digital surveillance is an adjunct to-not a replacement of-traditional surveillance and can trigger early investigation, diagnostics and responses at the regional level.

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Importance: COVID-19 was the underlying cause of death for more than 940 000 individuals in the US, including at least 1289 children and young people (CYP) aged 0 to 19 years, with at least 821 CYP deaths occurring in the 1-year period from August 1, 2021, to July 31, 2022. Because deaths among US CYP are rare, the mortality burden of COVID-19 in CYP is best understood in the context of all other causes of CYP death.

Objective: To determine whether COVID-19 is a leading (top 10) cause of death in CYP in the US.

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There has been substantial research on adult COVID-19 and how to treat it. But how do severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections afflict children? The COVID-19 pandemic has yielded many surprises, not least that children generally develop less severe disease than older adults, which is unusual for a respiratory disease. However, some children can develop serious complications from COVID-19, such as multisystem inflammatory syndrome in children (MIS-C) and Long Covid, even after mild or asymptomatic COVID-19.

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Background: Long Covid is a public health concern that needs defining, quantifying, and describing. We aimed to explore the initial and ongoing symptoms of Long Covid following SARS-CoV-2 infection and describe its impact on daily life.

Methods: We collected self-reported data through an online survey using convenience non-probability sampling.

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Article Synopsis
  • The study investigates how genetic variations influence blood-related traits in two isolated populations from the Mediterranean, focusing on individuals from Crete and the Pomak villages in Greece.
  • Researchers performed a genome-wide association scan, identifying five rare non-coding genetic variants significantly impacting blood cell counts and distribution.
  • A notable portion of the populations carries harmful mutations in the Haemoglobin Subunit Beta (HBB) gene, with distinct mutations prevalent in each group, highlighting the genetic diversity and its effects on various health-related traits.
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Objective: To offer a quantitative risk-benefit analysis of two doses of SARS-CoV-2 vaccination among adolescents in England.

Setting: England.

Design: Following the risk-benefit analysis methodology carried out by the US Centers for Disease Control, we calculated historical rates of hospital admission, Intensive Care Unit admission and death for ascertained SARS-CoV-2 cases in children aged 12-17 in England.

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Article Synopsis
  • SARS-CoV-2 has led to over 231 million infections and 4.7 million deaths globally as of late September 2021.
  • Some countries have implemented strict Zero COVID policies to keep infection rates near zero, while others in Europe and North America have opted for varying mitigation strategies to protect health systems.
  • The text discusses the long-term risks associated with COVID-19, including potential for viral mutations, persistent infections, reinfections, immune issues, and complications like Long COVID.
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Objectives: To assess the potential impacts of successive lockdown-easing measures in England, at a point in the COVID-19 pandemic when community transmission levels were relatively high.

Design: We developed a Bayesian model to infer incident cases and reproduction number () in England, from incident death data. We then used this to forecast excess cases and deaths in multiple plausible scenarios in which increases at one or more time points.

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Pharmacogenomics is increasingly moving into mainstream clinical practice. Careful consideration must be paid to inclusion of diverse populations in research, translation and implementation, in the historical and social context of population stratification, to ensure that this leads to improvements in healthcare for all rather than increased health disparities. This review takes a broad and critical approach to the current role of diversity in pharmacogenomics and addresses potential pitfalls in order to raise awareness for prescribers.

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