188 research outputs found

    γ-Glutamyltransferase and breast cancer risk beyond alcohol consumption and other life style factors - A pooled cohort analysis

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    Objective: Elevated γ-Glutamyltransferase serum levels are associated with increased risk of overall cancer incidence and several site-specific malignancies. In the present prospective study we report on the associations of serum γ-Glutamyltransferase with the risk of breast cancer in a pooled population-based cohort considering established life style risk factors. Methods: Two cohorts were included in the present study, i.e. the Vorarlberg (n = 97,268) and the Malmoe cohort (n = 9,790). Cox proportional hazards regression models were fitted to estimate HRs for risk of breast cancer. Results: In multivariate analysis adjusted for age, bodymass index and smoking status, women with γ- Glutamyltransferase levels in the top quartile were at significantly higher risk for breast cancer compared to women in the lowest quartile (HR 1.21, 95%CI 1.09 to 1.35; p = 0.005). In the subgroup analysis of theMalmoe cohort, γ-Glutamyltransferase remained an independent risk factor for breast cancer when additionally considering alcohol intake. A statistically significant increase in risk was seen in women with γ-Glutamyltransferase-levels in the top versus lowest quartile in a multivariate model adjusted for age, body mass index, smoking status, physical activity, parity, oral contraceptive-use and alcohol consumption (HR 1.37, 95% CI 1.11-1.69, p = 0.006). Conclusion: Our findings identified γ-Glutamyltransferase as an independent risk factor for breast cancer beyond the consumption of alcohol and other life style risk factors

    Hans Albrecht von Sprinzenstein

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    Mineral oil in human tissues, Part II: Characterization of the accumulated hydrocarbons by comprehensive two-dimensional gas chromatography

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    Mineral oil hydrocarbons are by far the largest contaminant in the human body. Their composition differs from that in the mineral oils humans are exposed to, and varies also between different tissues of the same individual. Using the presently best technique for characterizing the composition of mineral oil hydrocarbons, comprehensive two-dimensional gas chromatography (GC × GC), the hydrocarbons in human tissues were compared to those of various mineral oils. This provided information about the strongly accumulated species and might give hints on the flow path through the human body. The selectivity of accumulation is probably also of interest for the risk assessment of synthetic hydrocarbons (polyolefins). GC × GC grouped the MOSH into classes of n-alkanes, paraffins with a low degree of branching, multibranched paraffins and naphthenes (alkylated cyclic hydrocarbons) with 1–4 rings. Metabolic elimination was observed for constituents of all these classes, but was selective within each class. The MOSH in the subcutaneous abdominal fat tissues and the mesenteric lymph nodes (MLN) had almost the same composition and included the distinct signals observed in mineral oil, though in reduced amounts relative to the cloud of unresolved hydrocarbons. The MOSH in the liver and the spleen were different from those in the MLN and fat tissue, but again with largely identical composition for a given individual. Virtually all constituents forming distinct signals were eliminated, leaving an unresolved residue of highly isomerized hydrocarbons. [ABSTRACT FROM AUTHOR

    Preventing overdiagnosis in mammography screening – a public health perspective

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    AbstractPrevention and management of breast cancer in order to provide high quality health care is an important public health issue. The existence of overdiagnosis for breast-cancer was controversial for a long time but is now broadly accepted. Overdiagnosis is defined as the diagnosis of “disease” that will never cause symptoms or death during a patient’s ordinarily expected lifetime. Estimates of the overdiagnosis rate for breast cancer range up to 54% of screen-detected localized tumors. New approaches, such as the identification of high risk groups or primary prevention approaches could be more relevant from the public health perspective.</jats:p

    The relative risk of second primary cancers in Austria's western states: a retrospective cohort study

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    BACKGROUND: Cancer survivors are at risk of developing a second primary cancer (SPC) later in life because of persisting effects of genetic and behavioural risk factors, the long-term sequelae of chemotherapy, radiotherapy and the passage of time. This is the first study with Austrian data on an array of entities, estimating the risk of SPCs in a population-based study by calculating standardized incidence ratios (SIRs).METHODS: This retrospective cohort study included all invasive incident cancer cases diagnosed within the years 1988 to 2005 being registered in the Tyrol and Vorarlberg Cancer Registries. Person years at risk (PYAR) were calculated from time of first diagnosis plus 2\ua0months until the exit date, defined as the date of diagnosis of the SPC, date of death, or end of 2010, whichever came first. SIR for specific SPCs was calculated based on the risk of these patients for this specific cancer.RESULTS: A total of 59,638 patients were diagnosed with cancer between 1988 and 2005 and 4949 SPCs were observed in 399,535 person-years of follow-up (median 5.7\ua0years). Overall, neither males (SIR 0.90; 95% CI 0.86-0.93) nor females (SIR 1.00; 95% CI 0.96-1.05) had a significantly increased SIR of developing a SPC. The SIR for SPC decreased with age showing a SIR of 1.24 (95% CI 1.12-1.35) in the age group of 15-49 and a SIR of 0.85 (95% CI 0.82-0.89) in the age group of ≥ 65. If the site of the first primary cancer was head/neck/larynx cancer in males and females (SIR 1.88, 95% CI 1.67-2.11 and 1.74, 95% CI 1.30-2.28), cervix cancer in females (SIR 1.40, 95% CI 1.14-1.70), bladder cancer in males (SIR 1.20, 95% CI 1.07-1.34), kidney cancer in males and females (SIR 1.22, 95% 1.04-1.42 and 1.29, 95% CI 1.03-1.59), thyroid gland cancer in females (SIR 1.40, 95% CI 1.11-1.75), patients showed elevated SIR, developing a SPC.CONCLUSIONS: Survivors of head & neck, bladder/kidney, thyroid cancer and younger patients show elevated SIRs, developing a SPC. This has possible implications for surveillance strategies

    Effect of secular trend, age, and length of follow-up on optimum body mass index from 1985 to 2015 in a large Austrian cohort

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    Background Obesity and its health consequences will dominate health care systems in many countries during the next decades. However, the body mass index (BMI) optimum in relation to all-cause mortality is still a matter of debate. Material and Methods Data of the Vorarlberg Health Monitoring & Prevention Program (VHM&PP, 1985-2005) and data provided by the Main Association of Austrian Social Security Institutions (MAASSI, 2005-2015) were analyzed. Information was available on age, sex, smoking status, measured height and weight, and mortality. Generalized additive models were used to model mortality as a function of BMI, calendar time, age, and follow-up. Results In MAASSI (N=282,216, 46.0% men), men and women were on average 2.7 years older than in VHM&PP (N=185,361, 46.1% men). Average BMI was slightly higher in men (26.1 vs. 25.7 kg/m2) but not in women (24.6 vs. 24.7 kg/m2). We found an interactive effect of age and follow-up on the BMI optimum. Over age 35 in men and 55 years in women, the BMI optimum decreased with length of follow-up. While keeping covariates fixed, BMI optimum increased slightly between 1985 and 2015 in men and women, 24.9 (95%-CI, 23.9-25.9) to 26.4 (25.3-27.3), and 22.4 (21.7-23.1) to 23.3 (22.6-24.5) kg/m2, respectively. Conclusion Age and length of follow-up have a pronounced effect on the BMI associated with the lowest all-cause mortality. After controlling for age and length of follow-up, the BMI optimum increased slightly over 30 years in this large study sample

    [Stammbuch Paul Baumgartner]

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    [STAMMBUCH PAUL BAUMGARTNER] [Stammbuch Paul Baumgartner] ( - ) Cover ( - ) Notiz von Bibliothekar Preller, vorderer Spiegel (1r) Illustration und Register (1v 2r) Scherffenberg, Friedrich von; Blatt 10 (9v-10r) Prag zu Windhag, Friedrich von; Blatt 11 (11v-12r) Losenstein, Georg Achaz zu; Blatt 12 (11v-12r) Losenstein, Franz Adam zu; Blatt 13 (13v-14r) Puchheim, Wolf Adam von; Blatt 14 (14v-15r) Ostrorog, Nikolaus; Blatt 16 (16v-17r) Tschernembl, Georg Erasmus von; Blatt 19 (18v-19r) Tschernembl, Johannes Christoph von; Blatt 19 (18v-19r) Tschernembl, Heinrich von; Blatt 19 (19v-20r) Maxlrain, Georg von; Blatt 20 (19v-20r) Oettingen, Wipert von; Blatt 21 (20v-21r) Oettingen, Philipp von; Blatt 22 (21v-22r) Wchynsky zu Wchynicz, Wenceslaus; Blatt 23 (22v-23r) Wchynsky zu Wchynicz, Rudolph; Blatt 23 (23v-24r) Wchynsky zu Wchynicz, Johannes; Blatt 24 (23v-24r) Rogendorf und Mollenburg, Caspar von; Blatt 25 (24v-25r) Presing, Rudolf von; Blatt 25 (25v-26r) Dwořecky von Olbramowitz, Hans; Blatt 26 (25v-26r) Dwořecky von Olbramowitz, Prokop; Blatt 27 (26v-27r) Thanhausen, Wilhelm von; Blatt 28 (27v-28r) Welzer, Johannes; Blatt 30 (30v-31r) Welzer, Georg Rupert; Blatt 30 (30v-31r) Welzer, Bernhard; Blatt 30 (30v-31r) Losenstein, Wolf Siegmund von; Blatt 32 (31v-32r) Thüngen, Karl von; Blatt 33 (32v-33r) Tschetschau, Joachim von; Blatt 34 (34v-35r) Schönkirchen, Ferdinand von; Blatt 37 (36v-37r) Wolfstein, Johann Adam von; Blatt 38 (37v-38r) Wolffstein, Johann Albrecht von; Blatt 38 (38v-39r) Starhemberg, Hans Ulrich von; Blatt 40 (39v-40r) Concin, Hans Gabriel von; Blatt 44 (43v-44r) Pennzinger, Andre; Blatt 46 (45v-47r) Tannberg, Hans Jörg von; Blatt 46 (45v-47r) Neidhardt zu Gneisenau, Hans Wolf von; Blatt 47 (45v-47r) Herleinsberger, Heinrich; Blatt 47 (45v-47r) Oedt, Hans Christoph von; Blatt 47 (45v-47r) Schlux, Jeremias; Blatt 47 (45v-47r) Tannberg, Moritz von; Blatt 47 (45v-47r) Schleinitz, Christoph von; Blatt 47 (47v-48r) Haidersreuter, Achaz; Blatt 47 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    Changes of body mass index in relation to mortality: results of a cohort of 42,099 adults.

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    BackgroundHigh Body-Mass-Index (BMI) is associated with increased all-cause mortality, but little is known about the effect of short- and long-term BMI change on mortality. The aim of the study was to determine how long-term weight change affects mortality.Methods and findingsWithin a population-based prospective cohort of 42,099 Austrian men and women (mean age 43 years) with at least three BMI measurements we investigated the relationship of BMI at baseline and two subsequent BMI change intervals of five years each with all-cause mortality using Cox proportional Hazard models. During median follow-up of 12 years 4,119 deaths were identified. The lowest mortalities were found in persons with normal weight or overweight at baseline and stable BMI over 10 years. Weight gain (≥0.10 kg/m(2)/year) during the first five years was associated with increased mortality in overweight and obese people. For weight gain during both time intervals mortality risk remained significantly increased only in overweight (Hazard Ratio (HR): 1.39 (95% confidence interval: 1.01; 1.92)) and obese women (1.85 (95% confidence interval: 1.18; 2.89)). Weight loss (ConclusionOur findings highlight the importance of weight stability and obesity avoidance in prevention strategy
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