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Sökning: WFRF:(Harrison F.)

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631.
  • Glasser, N. F., et al. (författare)
  • Global sea-level contribution from the Patagonian Icefields since the Little Ice Age maximum
  • 2011
  • Ingår i: Nature Geoscience. - 1752-0894 .- 1752-0908. ; 4:5, s. 303-307
  • Tidskriftsartikel (refereegranskat)abstract
    • The melting of mountain glaciers and ice caps is expected to contribute significantly to sea-level rise in the twenty-first century(1-)3, although the magnitude of this contribution is not fully constrained. Glaciers in the Patagonian Icefields of South America are thought to have contributed about 10% of the total sea-level rise attributable to mountain glaciers in the past 50 years(3). However, it is unclear whether recent rates of glacier recession in Patagonia are unusual relative to the past few centuries. Here we reconstruct the recession of these glaciers using remote sensing and field determinations of trimline and terminal moraine location. We estimate that the North Patagonian Icefield has lost 103 +/- 20.7 km(3) of ice since its late Holocene peak extent in AD 1870 and that the South Patagonian Icefield has lost 503 +/- 101.1 km(3) since its peak in AD 1650. This equates to a sea-level contribution of 0.0018 +/- 0.0004 mm yr(-1) since 1870 from the north and 0.0034 +/- 0.0007 mm yr(-1) since 1650 from the south. The centennial rates of sea-level contribution we derive are one order of magnitude lower than estimates of melting over the past 50 years(3), even when we account for possible thinning above the trimline. We conclude that the melt rate and sea-level contribution of the Patagonian Icefields increased markedly in the twentieth century.
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632.
  • Glasser, Neil F., et al. (författare)
  • Younger Dryas and early Holocene age glacier advances in Patagonia
  • 2012
  • Ingår i: Quaternary Science Reviews. - : Elsevier BV. - 0277-3791 .- 1873-457X. ; 58, s. 7-17
  • Tidskriftsartikel (refereegranskat)abstract
    • Reliable dating of Southern Hemisphere glacier fluctuations since the Last Glacial Maximum (LGM) is crucial to resolving debates about millennial-scale climate change. Here we present Be-10 dates for lateral, valley-mouth and cross-valley moraines formed between the contemporary South American North Patagonian Icefield (NPI) and its LGM position in four separate valleys around 47 degrees S. This is an area near the core of the precipitation-bearing southern westerly winds, where it is known that rapid shifts in climate occurred during Lateglacial times. The dates indicate that outlet glaciers advanced, or at least stabilised, to form large moraines east of an expanded NPI at 11.0 +/- 0.5/11.2 +/- 0.6, 11.5 +/- 0.6, 11.7 +/- 0.6 and 12.8 +/- 0.7 ka (Putnam southern-hemisphere production rates and Dunai scaling scheme, assumed boulder erosion rate of 2 mm/ka). Four of these ages are statistically indistinguishable and probably represent a single, regional ice advance. The dates indicate that glaciers in Patagonia were larger during these times than at any point since the LGM and provide evidence in Patagonia for glacier advances around the time of the European Younger Dryas (12.9-11.7 ka) and into the very early Holocene. Although palaeoclimatic records from this area are often contradictory, these glacier advances were probably associated with a period of cooling or regionally increased precipitation related to the changes in the position of the southern westerly winds.
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633.
  • Gonzalez-Ortiz, Fernando, et al. (författare)
  • Preanalytical stability of plasma/serum brain-derived tau
  • 2023
  • Ingår i: Alzheimers & Dementia. - 1552-5260. ; 19:10, s. 4764-4770
  • Tidskriftsartikel (refereegranskat)abstract
    • INTRODUCTIONWe investigated the effects of matrix type and reagent batch changes on diagnostic performances and longitudinal trajectories of brain-derived tau (BD-tau). METHODSWe evaluated (i) Cohort 1: paired EDTA plasma and serum from Alzheimer biomarker-positive older adults versus controls (n = 26); and (ii) Cohort 2: n = 79 acute ischemic stroke patients with 265 longitudinal samples across four time points. RESULTSIn Cohort 1, plasma and serum BD-tau were strongly correlated (rho = 0.96, p < 0.0001) with similar diagnostic performances (AUCs >99%) and correlations with CSF total-tau (rho = 0.93-0.94, p < 0.0001). However, absolute concentrations were similar to 40% higher in plasma versus serum. In Cohort 2, first and repeated BD-tau measurements showed a near-perfect correlation (rho = 0.96, p < 0.0001), with no significant between-batch concentration differences. In longitudinal analyses, substituting similar to 10% of the first-run concentrations for the remeasured values showed overlapping estimated trajectories without significant differences at any time point. DISCUSSIONBD-tau has equivalent diagnostic accuracies, but non-interchangeable absolute concentrations, in plasma versus serum. Furthermore, the analytical robustness is unaffected by batch-to-batch reagent variations. HighlightsBrain-derived tau (BD-tau) is a novel blood-based biomarker that quantifies tau protein of CNS origin.Effects of preanalytical handling procedures on the quality and reproducibility of BD-tau measures are unknown.In two cohorts of n = 105 participants, we compared BD-tau concentrations and diagnostic performances in paired plasma and serum samples, and evaluated impacts of batch-to-batch reagent variations.Paired plasma and serum showed equivalent diagnostic performances to separate amyloid-positive AD from amyloid-negative controls, indicating both can be used independently.Repeated measurements and longitudinal trajectories of plasma BD-tau were unaffected by batch-to-batch reagent variation.
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634.
  • Gunnell, D, et al. (författare)
  • Associations between premorbid intellectual performance, early-life exposures and early-onset schizophrenia. Cohort study
  • 2002
  • Ingår i: The British journal of psychiatry : the journal of mental science. - : Royal College of Psychiatrists. - 0007-1250. ; 181, s. 298-305
  • Tidskriftsartikel (refereegranskat)abstract
    • Impaired intellectual performance is associated with an increased risk of schizophrenia.AimsTo investigate whether this association is due to the influence of prenatal and early childhood exposures on both intellectual development and the risk of schizophrenia.MethodCohort of 197 613 Swedish male conscripts with linked birth, census and hospital admission data together with five measures of verbal and non-verbal intellectual performance recorded at conscription. Results 109 643 subjects had complete data; over a mean 5-year follow-up, 60 developed schizophrenia and 92 developed other non-affective psychoses. Poor scores for each of the five tests were associated with 3-to 14-fold increased risk of psychosis, particularly schizophrenia. Controlling for birth-related exposures, including birth weight, and parental education did not attenuate these associations.Results109 643 subjects had complete data; over amean 5-year follow-up,60 developed schizophrenia and 92 developed other non-affective psychoses. Poor scores for each of the five testswere associatedwith 3-to 14-foldincreasedrisk of psychosis, particularly schizophrenia. Controlling for birth-related exposures, including birthweight, and parental education didnot attenuate these associations.ConclusionsPoor intellectual performance at 18 years of age is associated with early-onset psychotic disorder. Associations do not appear to be confounded by prenatal adversity or childhood circumstances, as indexed by parental education.
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635.
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636.
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637.
  • Halliday, Alison, et al. (författare)
  • 10-year stroke prevention after successful carotid endarterectomy for asymptomatic stenosis (ACST-1) : A multicentre randomised trial
  • 2010
  • Ingår i: The Lancet. - 0140-6736 .- 1474-547X. ; 376:9746, s. 1074-1084
  • Tidskriftsartikel (refereegranskat)abstract
    • Background If carotid artery narrowing remains asymptomatic (ie, has caused no recent stroke or other neurological symptoms), successful carotid endarterectomy (CEA) reduces stroke incidence for some years. We assessed the long-term effects of successful CEA. Methods Between 1993 and 2003, 3120 asymptomatic patients from 126 centres in 30 countries were allocated equally, by blinded minimised randomisation, to immediate CEA (median delay 1 month, IQR 0·3-2·5) or to indefinite deferral of any carotid procedure, and were followed up until death or for a median among survivors of 9 years (IQR 6-11). The primary outcomes were perioperative mortality and morbidity (death or stroke within 30 days) and non-perioperative stroke. Kaplan-Meier percentages and logrank p values are from intention-to-treat analyses. This study is registered, number ISRCTN26156392. Findings 1560 patients were allocated immediate CEA versus 1560 allocated deferral of any carotid procedure. The proportions operated on while still asymptomatic were 89·7 versus 4·8 at 1 year (and 92·1 vs 16·5 at 5 years). Perioperative risk of stroke or death within 30 days was 3·0 (95 CI 2·4-3·9; 26 non-disabling strokes plus 34 disabling or fatal perioperative events in 1979 CEAs). Excluding perioperative events and non-stroke mortality, stroke risks (immediate vs deferred CEA) were 4·1 versus 10·0 at 5 years (gain 5·9, 95 CI 4·0-7·8) and 10·8 versus 16·9 at 10 years (gain 6·1, 2·7-9·4); ratio of stroke incidence rates 0·54, 95 CI 0·43-0·68, p<0·0001. 62 versus 104 had a disabling or fatal stroke, and 37 versus 84 others had a non-disabling stroke. Combining perioperative events and strokes, net risks were 6·9 versus 10·9 at 5 years (gain 4·1, 2·0-6·2) and 13·4 versus 17·9 at 10 years (gain 4·6, 1·2-7·9). Medication was similar in both groups; throughout the study, most were on antithrombotic and antihypertensive therapy. Net benefits were significant both for those on lipid-lowering therapy and for those not, and both for men and for women up to 75 years of age at entry (although not for older patients). Interpretation Successful CEA for asymptomatic patients younger than 75 years of age reduces 10-year stroke risks. Half this reduction is in disabling or fatal strokes. Net benefit in future patients will depend on their risks from unoperated carotid lesions (which will be reduced by medication), on future surgical risks (which might differ from those in trials), and on whether life expectancy exceeds 10 years. Funding UK Medical Research Council, BUPA Foundation, Stroke Association.
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638.
  • Harrison, C. J., et al. (författare)
  • An international study of intrachromosomal amplification of chromosome 21 (iAMP21) : cytogenetic characterization and outcome
  • 2014
  • Ingår i: Leukemia. - : Springer Science and Business Media LLC. - 0887-6924 .- 1476-5551. ; 28:5, s. 1015-1021
  • Tidskriftsartikel (refereegranskat)abstract
    • Intrachromosomal amplification of chromosome 21 (iAMP21) defines a distinct cytogenetic subgroup of childhood B-cell precursor acute lymphoblastic leukaemia (BCP-ALL). To date, fluorescence in situ hybridisation (FISH), with probes specific for the RUNX1 gene, provides the only reliable detection method (five or more RUNX1 signals per cell). Patients with iAMP21 are older (median age 9 years) with a low white cell count. Previously, we demonstrated a high relapse risk when these patients were treated as standard risk. Recent studies have shown improved outcome on intensive therapy. In view of these treatment implications, accurate identification is essential. Here we have studied the cytogenetics and outcome of 530 iAMP21 patients that highlighted the association of specific secondary chromosomal and genetic changes with iAMP21 to assist in diagnosis, including the gain of chromosome X, loss or deletion of chromosome 7, ETV6 and RB1 deletions. These iAMP21 patients when treated as high risk showed the same improved outcome as those in trial-based studies regardless of the backbone chemotherapy regimen given. This study reinforces the importance of intensified treatment to reduce the risk of relapse in iAMP21 patients. This now well-defined patient subgroup should be recognised by World Health Organisation (WHO) as a distinct entity of BCP-ALL.
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639.
  • Harrison, G, et al. (författare)
  • Association between psychotic disorder and urban place of birth is not mediated by obstetric complications or childhood socio-economic position: a cohort study
  • 2003
  • Ingår i: Psychological medicine. - : Cambridge University Press (CUP). - 0033-2917 .- 1469-8978. ; 33:4, s. 723-731
  • Tidskriftsartikel (refereegranskat)abstract
    • Background. Although urban place of birth has been identified as a risk factor for schizophrenia, the extent to which this association is mediated by socially patterned risk factors such as obstetric complications and childhood socio-economic position is unclear. The diagnostic specificity of the association within the clinical psychotic syndromes is also unclear.Method. A population cohort of 696025 males and females, born in Sweden between 1973 and 1980 and with linked birth and socio-economic data was followed up from age 16 for up to 9·8 years. Hospitalized cases of schizophrenia and other non-affective psychosis were identified from the Swedish Inpatient Discharge Register. We examined associations of these disorders with a three-level measure of urbanicity of birthplace before and after controlling for measures of foetal nutrition, obstetric complications and level of maternal education.Results. Urban compared to rural birthplace was associated both with increased risk of adult onset schizophrenia (hazard ratio 1·34, CI 0·91–1·96) and other non-affective psychoses (hazard ratio 1·63, CI 1·18–2·26). None of these associations was greatly affected by adjustment for obstetric complications or maternal educational level. In the group of other non-affective psychoses urban–rural differences in disease risk were strongest among those born in the winter months.Conclusion. Urbanization of birthplace is associated with increased risk of non-affective psychosis but this is not confined to narrowly defined cases. The magnitude of the association in Sweden is lower than that reported in other studies. Causal factors underlying this association appear to operate independently of risks associated with obstetric complications and parental educational status.
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640.
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