SwePub
Tyck till om SwePub Sök här!
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Pedersen M.) "

Sökning: WFRF:(Pedersen M.)

  • Resultat 1851-1860 av 1872
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1851.
  • Wästerlid, Tove, et al. (författare)
  • Impact of chemotherapy regimen and rituximab in adult Burkitt lymphoma : a retrospective population-based study from the Nordic Lymphoma Group
  • 2013
  • Ingår i: Annals of Oncology. - : Elsevier BV. - 0923-7534 .- 1569-8041. ; 24:7, s. 1879-1886
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Standard treatment of adult Burkitt lymphoma is not defined due to the lack of randomised trials. In this situation, population-based data may represent a useful contribution in order to identify an optimal treatment strategy. Patients and methods: The aims of this study were to investigate the outcome for adult HIV-negative BL with different chemotherapy regimens, and to assess possible improvement within the time frame of the study. The study population was identified through the Swedish and Danish lymphoma registries 2000-2009. Results: A total of 258 patients were identified. Since 2000, overall survival (OS) improved significantly only for younger patients (<65 years). Intensive regimens such as the Berlin-Frankfurt-Munster, hyper-fractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (hyper-CVAD) and cyclophosphamide, vincristine, doxorubicin, methotrexate, ifosfamide, etoposide, and cytarabine (CODOX-M/IVAC) were associated with a favourable 2-year OS of 82%, 83%, and 69%, respectively. The low-intensive CHOP/CHOEP regimens achieved a 2-year OS of 38.8%, confirming their inadequacy for the treatment of BL. In a multivariate analysis, rituximab was not significantly associated with improved OS. Conclusions: In this population-based retrospective series of adult BL, intensive chemotherapy regimens were associated with favourable outcome. The impact of the addition of rituximab remains uncertain and warrants further investigation.
  •  
1852.
  • Xie, Weijia, et al. (författare)
  • Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes
  • 2013
  • Ingår i: Diabetes. - : American Diabetes Association. - 0012-1797 .- 1939-327X. ; 62:6, s. 2141-2150
  • Tidskriftsartikel (refereegranskat)abstract
    • Circulating metabolites associated with insulin sensitivity may represent useful biomarkers, but their causal role in insulin sensitivity and diabetes is less certain. We previously identified novel metabolites correlated with insulin sensitivity measured by the hyperinsulinemic-euglycemic clamp. The top-ranking metabolites were in the glutathione and glycine biosynthesis pathways. We aimed to identify common genetic variants associated with metabolites in these pathways and test their role in insulin sensitivity and type 2 diabetes. With 1,004 nondiabetic individuals from the RISC study, we performed a genome-wide association study (GWAS) of 14 insulin sensitivity–related metabolites and one metabolite ratio. We replicated our results in the Botnia study (n = 342). We assessed the association of these variants with diabetes-related traits in GWAS meta-analyses (GENESIS [including RISC, EUGENE2, and Stanford], MAGIC, and DIAGRAM). We identified four associations with three metabolites—glycine (rs715 at CPS1), serine (rs478093 at PHGDH), and betaine (rs499368 at SLC6A12; rs17823642 at BHMT)—and one association signal with glycine-to-serine ratio (rs1107366 at ALDH1L1). There was no robust evidence for association between these variants and insulin resistance or diabetes. Genetic variants associated with genes in the glycine biosynthesis pathways do not provide consistent evidence for a role of glycine in diabetes-related traits.
  •  
1853.
  • Xu, W. L., et al. (författare)
  • Midlife overweight and obesity increase late-life dementia risk : a population-based twin study
  • 2011
  • Ingår i: Neurology. - 0028-3878 .- 1526-632X. ; 76:18, s. 1568-1574
  • Tidskriftsartikel (refereegranskat)abstract
    • Objective: The relation of overweight to dementia is controversial. We aimed to examine the association of midlife overweight and obesity with dementia, Alzheimer disease (AD), and vascular dementia (VaD) in late life, and to verify the hypothesis that genetic and early-life environmental factors contribute to the observed association.Methods: From the Swedish Twin Registry, 8,534 twin individuals aged ≥65 (mean age 74.4) were assessed to detect dementia cases (DSM-IV criteria). Height and weight at midlife (mean age 43.4) were available in the Registry. Data were analyzed as follows: 1) unmatched case-control analysis for all twins using generalized estimating equation (GEE) models and 2) cotwin matched case-control approach for dementia-discordant twin pairs by conditional logistic regression taking into account lifespan vascular disorders and diabetes.Results: Among all participants, dementia was diagnosed in 350 subjects, and 114 persons had questionable dementia. Overweight (body mass index [BMI] >25-30) and obesity (BMI >30) at midlife were present in 2,541 (29.8%) individuals. In fully adjusted GEE models, compared with normal BMI (20-25), overweight and obesity at midlife were related to dementia with odds ratios (ORs) (95% CIs) of 1.71 (1.30-2.25) and 3.88 (2.12-7.11), respectively. Conditional logistic regression analysis in 137 dementia-discordant twin pairs led to an attenuated midlife BMI-dementia association. The difference in ORs from the GEE and the matched case-control analysis was statistically significant (p = 0.019).Conclusions: Both overweight and obesity at midlife independently increase the risk of dementia, AD, and VaD. Genetic and early-life environmental factors may contribute to the midlife high adiposity-dementia association.
  •  
1854.
  • Xu, W., et al. (författare)
  • Mid- and late-life diabetes in relation to the risk of dementia: a population-based twin study.
  • 2009
  • Ingår i: Diabetes. - : American Diabetes Association. - 1939-327X .- 0012-1797. ; 58:1, s. 71-77
  • Tidskriftsartikel (refereegranskat)abstract
    • OBJECTIVE: We aimed to verify the association between diabetes and the risk of dementia, Alzheimer's disease, and vascular dementia in twins and to explore whether genetic and early-life environmental factors could contribute to this association. RESEARCH DESIGN AND METHODS: This study included 13,693 twin individuals aged > or =65 years. Dementia was diagnosed according to DSM-IV (Diagnostic Manual of Mental Disorders, 4th ed.) criteria. Information on diabetes was collected from the inpatient registry and self- or informant-reported history of diabetes. Data were analyzed following two strategies: 1) unmatched case-control analysis for all participants using generalized estimating equation (GEE) models and 2) cotwin matched case-control analysis for dementia-discordant twin pairs using conditional logistic regression. RESULTS: Of all participants, 467 were diagnosed with dementia, including 292 with Alzheimer's disease and 105 with vascular dementia, and an additional 170 were diagnosed with questionable dementia. Diabetes was present in 1,396 subjects. In GEE models, diabetes was associated with adjusted odds ratios (ORs) (95% CI) of 1.89 (1.51-2.38) for dementia, 1.69 (1.16-2.36) for Alzheimer's disease, and 2.17 (1.36-3.47) for vascular dementia. Compared with late-life diabetes (onset age > or =65 years), the risk effect of mid-life diabetes (onset age <65 years) on dementia was stronger. Conditional logistic analysis of 210 dementia-discordant twin pairs led to ORs of 2.41 (1.05-5.51) and 0.68 (0.30-1.53) for dementia related to mid- and late-life diabetes, respectively. CONCLUSIONS: Diabetes increases the risk of Alzheimer disease and vascular dementia. The risk is stronger when diabetes occurs at mid-life than in late life. Genetic and early-life environmental factors might contribute to the late-life diabetes-dementia association but could not account for the mid-life diabetes-dementia association.
  •  
1855.
  •  
1856.
  • Yli, Branka M., et al. (författare)
  • Intrapartum cardiotocography (CTG) and ST-analysis of labor in diabetic patients
  • 2011
  • Ingår i: Journal of Perinatal Medicine. - 1619-3997. ; 39:4, s. 457-465
  • Tidskriftsartikel (refereegranskat)abstract
    • Aim: To determine the prevalence and types of intrapartum cardiotocography (CTG) patterns and investigate their relationship to moderate acidemia in term fetuses of diabetic mothers. Also, to assess if the combination of fetal electrocardiogram (FECG) and those CTG patterns strengthens the association with moderate acidemia. Material and methods: The material for this study is obtained from the Swedish randomized control trial and the European Union ST-analysis trial. We developed an analytical model for CTG patterns based on the progress in CTG changes, in a longitudinal periodic manner. The model was then combined with information regarding changes in ST interval that indicate threatening asphyxia, and the findings were analyzed to determine correlation with the presence of moderate acidemia at birth. Results: This study involved data of 413 diabetic mothers. A preterminal CTG was more common in the diabetes mellitus (DM) group (6/70, 8.6%) than in the gestational diabetes (GD) group (3/307, 1.0%; P=0.003). For diabetic mothers (i.e., DM+GD) with a normal CTG at the start of monitoring, the presence of FECG data indicating asphyxia significantly increased the likelihood of an umbilical artery pH < 7.15 at birth wodds ratio (OR) = 3.65, 95% confidence interval (CI) = 1.33-10.05]. Among labors where the CTG was non-reassuring at the start of monitoring, no significant association was found between pH < 7.15 and indication to intervene according to FECG information (OR = 1.51, 95% CI = 0.33-7.0). Conclusions: A preterminal CTG is more common in the fetuses of DM than GD mothers during labor. When CTG was normal at the start of recording, the addition of FECG information gave a significant add on information to predict moderate acidemia.
  •  
1857.
  • Yli, Branka M, et al. (författare)
  • Intrapartum fetal ECG and diabetes
  • 2008
  • Ingår i: Journal of Maternal-Fetal & Neonatal Medicine. - : Informa UK Limited. - 1476-7058 .- 1476-4954. ; 21:4, s. 231-238
  • Tidskriftsartikel (refereegranskat)abstract
    • Aim. The objective of this study was to determine the prevalence and types of ST-segment changes of the fetal electrocardiogram (FECG) during labour in term fetuses born to mothers with diabetes mellitus (DM) or gestational diabetes. Methods. This was a retrospective case-control study involving populations from two multi centre trials: the Swedish Randomized Control Trial and the European Union ST-analysis (EU-STAN) trial. ST-segment changes were assessed in 104/309 cases and 207/468 controls from the Swedish and EU-STAN trials, respectively. Results. ST depression was present on the FECG in 22.1% of fetuses of mothers with DM compared to 12% of controls OR=2.6, 95% CI=1.4-4.7, p=0.002 after adjusting for trial, birth weight, and nulliparity. ST elevation was present in 47.1% of DM patients and 41.2% of controls (OR=1.4, 95% CI=0.9-2.3, p=0.18). Conclusion. ST depression on the FECG was significantly more prevalent in the fetuses of mothers with DM, probably not indicating hypoxia but an altered ability of the myocardium to respond to the stress of labour. Further studies into the mechanism of fetal compromise during diabetic labour, are required.
  •  
1858.
  •  
1859.
  •  
1860.
  • Yuh, Jongil, et al. (författare)
  • The role of temperament and social support in depressive symptoms: A twin study of mid-aged women
  • 2008
  • Ingår i: Journal of Affective Disorders. - : Elsevier BV. - 1573-2517 .- 0165-0327. ; 106:1-2, s. 99-105
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Although research has found that temperament and social support are associated with depression, these relationships have not been explored in conjunction with one another as they relate to depression using a genetically informative design. This study investigated how the association among the three constructs is mediated. Methods: The sample in this study consisted of 326 pairs of adult monozygotic and dizygotic twins drawn from the Swedish Twin Registry. Twins were mothers of adolescent from married or partnered relationships. The genetic and environmental contributions to the association were evaluated by self-reported measures of temperament, social support, and depressive symptoms. Results: Multivariate genetic model fitting revealed that a moderate portion of genetic influences were common among the three central constructs of harm avoidance, perceived social support, and depressive symptoms. Limitations: The results may not be generalizable to depressive disorders in clinical settings. The measures were self-reported from a cross-sectional study. Conclusions: The findings suggest that the heritable component may contribute to genetic influences on an individual's ability to secure social support and thus to genetic risk for depressive symptomatology in women.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1851-1860 av 1872
Typ av publikation
tidskriftsartikel (1641)
konferensbidrag (189)
forskningsöversikt (19)
annan publikation (6)
rapport (5)
bokkapitel (5)
visa fler...
doktorsavhandling (3)
samlingsverk (redaktörskap) (1)
proceedings (redaktörskap) (1)
visa färre...
Typ av innehåll
refereegranskat (1616)
övrigt vetenskapligt/konstnärligt (252)
populärvet., debatt m.m. (2)
Författare/redaktör
Pedersen, M. (274)
Wu, Y. (245)
Williams, S. (239)
Erdmann, J. (235)
Price, D. (232)
Liu, Y. (230)
visa fler...
Wang, J. (229)
Chen, C. (228)
Chen, H. (228)
Chen, X. (228)
Li, S. (228)
Yu, J. (228)
Chen, Y. (227)
Valero, A. (227)
Walker, R. (227)
Yang, Y. (227)
Li, H. (226)
Meyer, J. (226)
Nielsen, J. (226)
Wilson, A. (226)
Alonso, A. (225)
Esposito, B. (225)
Nakamura, T. (225)
Bai, Y. (224)
Chen, S. (224)
Fox, H. (224)
Francis, D. (224)
Jain, V. (224)
Jones, G. (224)
Li, B. (224)
Liu, M. (224)
Moreno, D. (224)
Owen, M. (224)
Schulz, H. (224)
Spagnolo, S. (224)
White, S. (224)
Young, C. (224)
Arai, Y. (223)
Howard, J. (223)
Jones, T. J. (223)
Mueller, T. (223)
Romano, M. (223)
Sanchez, A. (223)
Schneider, B. (223)
Silva, J. (223)
Wang, H. (223)
Wang, X. (223)
Xu, L. (223)
Yamada, M. (223)
Yamamoto, S. (223)
visa färre...
Lärosäte
Karolinska Institutet (936)
Lunds universitet (559)
Uppsala universitet (507)
Göteborgs universitet (294)
Stockholms universitet (266)
Kungliga Tekniska Högskolan (255)
visa fler...
Umeå universitet (136)
Jönköping University (68)
Linköpings universitet (57)
Chalmers tekniska högskola (45)
Örebro universitet (37)
RISE (20)
Högskolan i Skövde (14)
Mittuniversitetet (13)
Handelshögskolan i Stockholm (9)
Högskolan Dalarna (9)
Högskolan i Gävle (8)
Högskolan i Halmstad (5)
Malmö universitet (5)
Högskolan i Borås (4)
Naturhistoriska riksmuseet (4)
Luleå tekniska universitet (3)
Södertörns högskola (3)
Sveriges Lantbruksuniversitet (3)
Högskolan Kristianstad (2)
Linnéuniversitetet (2)
Karlstads universitet (2)
Blekinge Tekniska Högskola (2)
Högskolan Väst (1)
Gymnastik- och idrottshögskolan (1)
Röda Korsets Högskola (1)
visa färre...
Språk
Engelska (1863)
Svenska (6)
Danska (1)
Italienska (1)
Odefinierat språk (1)
Forskningsämne (UKÄ/SCB)
Medicin och hälsovetenskap (629)
Naturvetenskap (465)
Samhällsvetenskap (58)
Teknik (30)
Humaniora (7)
Lantbruksvetenskap (3)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy