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Sökning: WFRF:(Hunt )

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1.
  • Kanai, M, et al. (författare)
  • 2023
  • swepub:Mat__t
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  • 2021
  • swepub:Mat__t
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  • 2021
  • swepub:Mat__t
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  • Dunham, I, et al. (författare)
  • The DNA sequence of human chromosome 22
  • 1999
  • Ingår i: Nature. - : Springer Science and Business Media LLC. - 0028-0836 .- 1476-4687. ; 402:6761, s. 489-495
  • Tidskriftsartikel (refereegranskat)
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  • Gwynne, Steve, et al. (författare)
  • Methodology developed for field observations of large events during the pandemic
  • 2024
  • Ingår i: Safety Science. - 0925-7535. ; 176
  • Tidskriftsartikel (refereegranskat)abstract
    • The Events Research Programme (ERP) was a multi-disciplinary study undertaken during the COVID-19 pandemic to investigate SARS-CoV-2 transmission risks and mitigations around the reopening of mass events in the UK in 2021 – including a behavioural study, exploring how non-pharmaceutical interventions (NPIs), such as social distancing, pre-event virus testing, and the use of face coverings might enable people to attend events safely. This behavioural study is discussed here. A total of 21 pilot events were involved in the study between April and July 2021. The venues used for the pilots varied in size, layout, occupancy level, and crowd management approaches. Data was extracted from manual qualitative observations and venue CCTV cameras which recorded routinely at venues. In addition, 890 cameras were installed during the events to capture attendee movement outside the venues, during arrival, in event areas, circulation spaces, bars and restaurants, and on exiting. A mixed method approach was adopted to ensure locations and activities of interest were captured, quantitative data gathered, and that this data could be placed in context. This enabled a behavioural study, quantifying crowd performance behaviours for comparison between and within events. This paper describes the background to this work, the method adopted and provides a brief overview of the data collected, relating primarily to (i) crowd densities, (ii) social distancing (captured here as contact distancing), and (iii) the use of face coverings.
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10.
  • Haycock, Philip C., et al. (författare)
  • Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases A Mendelian Randomization Study
  • 2017
  • Ingår i: JAMA Oncology. - : American Medical Association. - 2374-2437 .- 2374-2445. ; 3:5, s. 636-651
  • Tidskriftsartikel (refereegranskat)abstract
    • IMPORTANCE: The causal direction and magnitude of the association between telomere length and incidence of cancer and non-neoplastic diseases is uncertain owing to the susceptibility of observational studies to confounding and reverse causation. OBJECTIVE: To conduct a Mendelian randomization study, using germline genetic variants as instrumental variables, to appraise the causal relevance of telomere length for risk of cancer and non-neoplastic diseases. DATA SOURCES: Genomewide association studies (GWAS) published up to January 15, 2015. STUDY SELECTION: GWAS of noncommunicable diseases that assayed germline genetic variation and did not select cohort or control participants on the basis of preexisting diseases. Of 163 GWAS of noncommunicable diseases identified, summary data from 103 were available. DATA EXTRACTION AND SYNTHESIS: Summary association statistics for single nucleotide polymorphisms (SNPs) that are strongly associated with telomere length in the general population. MAIN OUTCOMES AND MEASURES: Odds ratios (ORs) and 95% confidence intervals (CIs) for disease per standard deviation (SD) higher telomere length due to germline genetic variation. RESULTS: Summary data were available for 35 cancers and 48 non-neoplastic diseases, corresponding to 420 081 cases (median cases, 2526 per disease) and 1 093 105 controls (median, 6789 per disease). Increased telomere length due to germline genetic variation was generally associated with increased risk for site-specific cancers. The strongest associations (ORs [ 95% CIs] per 1-SD change in genetically increased telomere length) were observed for glioma, 5.27 (3.15-8.81); serous low-malignant-potential ovarian cancer, 4.35 (2.39-7.94); lung adenocarcinoma, 3.19 (2.40-4.22); neuroblastoma, 2.98 (1.92-4.62); bladder cancer, 2.19 (1.32-3.66); melanoma, 1.87 (1.55-2.26); testicular cancer, 1.76 (1.02-3.04); kidney cancer, 1.55 (1.08-2.23); and endometrial cancer, 1.31 (1.07-1.61). Associations were stronger for rarer cancers and at tissue sites with lower rates of stem cell division. There was generally little evidence of association between genetically increased telomere length and risk of psychiatric, autoimmune, inflammatory, diabetic, and other non-neoplastic diseases, except for coronary heart disease (OR, 0.78 [ 95% CI, 0.67-0.90]), abdominal aortic aneurysm (OR, 0.63 [ 95% CI, 0.49-0.81]), celiac disease (OR, 0.42 [ 95% CI, 0.28-0.61]) and interstitial lung disease (OR, 0.09 [ 95% CI, 0.05-0.15]). CONCLUSIONS AND RELEVANCE: It is likely that longer telomeres increase risk for several cancers but reduce risk for some non-neoplastic diseases, including cardiovascular diseases.
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