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1.
Cancer Causes Control ; 31(2): 203-207, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31823169

ABSTRACT

PURPOSE: Chronic inflammation has been implicated in endometrial carcinogenesis yet the impact of potentially modifiable exposures that might affect inflammation, like diet, has been understudied. This study examined the association between the dietary inflammatory index (DII®), a literature-derived tool to assess the inflammatory potential of diet, and risk of developing, and survival after a diagnosis of endometrial cancer (EC). METHODS: This study included data from 1,287 women with EC and 1,435 population controls who participated in the Australian National Endometrial Cancer Study. Energy-adjusted DII (E-DII) scores were calculated from pre-diagnostic dietary intake obtained using a semi-quantitative food frequency questionnaire. Logistic regression was used to assess the association between E-DII scores and risk of EC and proportional-hazards models were used for survival analyses. RESULTS: Higher E-DII scores, reflecting a more pro-inflammatory diet, were not associated with risk of EC [adjusted odds ratio (OR) 0.98, 95% CI 0.77-1.24, p-trend = 0.7]. However, in stratified analyses, higher E-DII scores were associated with increased risk of EC among very obese (BMI 35 + kg/m2) women (OR 1.60, 95% CI 0.80-3.21, p-trend = 0.049, p-interaction = 0.045). After a median follow-up of 7.2 years there were 160 deaths, of which 110 (69%) were from EC. We found no association between E-DII score and survival. CONCLUSION: Greater inflammatory potential of pre-diagnostic diet was not associated with EC risk or survival. Secondary stratified analysis suggested greater inflammatory potential may be associated with EC risk in very obese women.


Subject(s)
Diet , Endometrial Neoplasms/epidemiology , Inflammation/epidemiology , Obesity/epidemiology , Adolescent , Adult , Aged , Australia/epidemiology , Female , Humans , Logistic Models , Middle Aged , Odds Ratio , Risk Factors , Young Adult
2.
J Hum Nutr Diet ; 32(5): 667-675, 2019 10.
Article in English | MEDLINE | ID: mdl-31270891

ABSTRACT

BACKGROUND: Concerns associated with blended enteral feeds include the risk of blocked tubes and microbial contamination, although the available evidence is limited. The present laboratory-based investigation aimed to examine these risks in a blended feed providing a nutritionally adequate intake for a hypothetical patient. METHODS: A one-blended feed recipe was made using three different methods (professional, jug and stick blenders) and three storage procedures. Feed samples were syringed via 10-, 12- and 14-French (Fr) enteral feeding tubes and both blockages and the time taken were recorded. Feed samples were diluted, plated on agars, incubated and bacterial colony-forming units (CFU) counted. After storage at -80 °C, identification was undertaken using 16S rRNA polymerase chain reaction sequencing. RESULTS: Two blockages occurred during 27 administrations of feed made using a professional blender, although they were resolved with a water flush. No blockages occurred with the 14-Fr tube and administration was quicker with wider tubes (P < 0.00001). There was no significant difference between the total bacterial CFU of feeds prepared using different methods (P = 0.771) or stored differently. The genus of bacteria identified included Enterococcus, Bacillus, lactose-fermenting Enterobacteriaceae, Pseudomonas and Staphylococcus. Pathogens, such as Clostridium spp., Salmonella spp. and Vibrio spp., were not identified by phenotypic tests used. Sequencing identified Escherichia coli, Shigella spp., Streptococcus lutetiensis and Staphylococcus epidermidis. CONCLUSIONS: The present study found no risk of tube blockages when one blended feed recipe made using three methods was delivered via a 14-Fr tube. There is concern about bacterial contamination, although this was not influenced by the methods of preparation or storage used in the present study.


Subject(s)
Enteral Nutrition/adverse effects , Equipment Contamination , Food Handling/methods , Intubation, Gastrointestinal/adverse effects , Colony Count, Microbial , Enteral Nutrition/instrumentation , Enteral Nutrition/methods , Humans , Intubation, Gastrointestinal/instrumentation
3.
Eur J Nutr ; 58(4): 1757, 2019 06.
Article in English | MEDLINE | ID: mdl-30267201

ABSTRACT

In the original publication of this article on page 6, paragraph "Discussion", line 4, 'In a U.S. population-based case-control study (n = 493 cases) Peres et al., reported a non-significant association between DII score and risk of developing ovarian cancer of similar magnitude (OR DII scoreQ4 vs. Q1 1.35, 95% CI 0.93-1.97) [20]'. It should read as 'In a U.S. population-based case-control study (n = 493 cases) Peres et al., reported a significant association between DII score and risk of developing ovarian cancer (OR DII scoreQ4 vs. Q1 1.72, 95% CI 1.18-2.51) [20]'.

4.
Eur J Nutr ; 58(4): 1747-1756, 2019 Jun.
Article in English | MEDLINE | ID: mdl-30027314

ABSTRACT

PURPOSE: Inflammation has been implicated in ovarian carcinogenesis. This study evaluated two dietary indices: the Dietary Inflammatory Index (DII®) and the Empirical Dietary Inflammatory Pattern (EDIP), in relation to risk of developing, and survival following, a diagnosis of ovarian cancer. METHODS: Data came from the Australian Ovarian Cancer Study (1375 cases, 1415 population controls). DII and EDIP scores were computed from dietary information obtained using a semiquantitative food-frequency questionnaire. Logistic regression was used to assess the association between DII and EDIP scores and risk of ovarian cancer and proportional hazards models were used for survival analysis. RESULTS: A high DII score, reflecting a more pro-inflammatory diet, was associated with a modest increased risk of ovarian cancer [odds ratio (OR) DII scoreQ4 vs.Q1 = 1.31, 95% CI 1.06-1.63, ptrend = 0.014]. Likewise a high EDIP score was associated with an increase in risk of ovarian cancer [OR EDIP scoreQ4 vs.Q1 = 1.39, 95% confidence interval (CI) 1.12-1.73, ptrend = 0.002]. We found no association between DII or EDIP score and overall or ovarian cancer-specific survival. CONCLUSION: In conclusion, our results suggest that a pro-inflammatory diet modestly increases the risk of developing ovarian cancer.


Subject(s)
Diet/adverse effects , Inflammation/epidemiology , Ovarian Neoplasms/epidemiology , Adolescent , Adult , Aged , Australia/epidemiology , Comorbidity , Female , Humans , Middle Aged , Risk Factors , Survival Analysis , Young Adult
5.
Gynecol Oncol ; 150(1): 99-105, 2018 07.
Article in English | MEDLINE | ID: mdl-29706522

ABSTRACT

OBJECTIVE: Although endometrial cancer (EC) is associated with relatively good survival rates overall, women diagnosed with high-risk subtypes have poor outcomes. We examined the relationship between lifestyle factors and subsequent all-cause, cancer-specific and non-cancer related survival. METHODS: In a cohort of 1359 Australian women diagnosed with incident EC between 2005 and 2007 pre-diagnostic information was collected by interview at recruitment. Clinical and survival information was abstracted from women's medical records, supplemented by linkage to the Australian National Death Index. Cox proportional hazards regression was used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for all-cause and cause-specific survival (EC death vs. non-EC death) associated with each exposure, overall and by risk group (low-grade endometrioid vs. high-grade endometrioid and non-endometrioid). RESULTS: After a median follow-up of 7.1 years, 179 (13%) women had died, with 123 (69%) deaths from EC. As expected, elevated body mass index (BMI), diabetes and the presence of other co-morbidities were associated with a significantly increased risk of all-cause and non-cancer related death. Women with diabetes had higher cancer-specific mortality rates (HR 2.09, 95% CI 1.31-3.35), particularly those who had were not obese (HR 4.13, 95% CI 2.20-7.76). The presence of ≥2 other co-morbidities (excluding diabetes) was also associated with increased risk of cancer-specific mortality (HR 3.09, 95% CI 1.21-7.89). The patterns were generally similar for women with low-grade and high-grade endometrioid/non-endometrioid EC. CONCLUSION: Our findings demonstrate the importance of diabetes, other co-morbidities and obesity as negative predictors of mortality among women with EC but that the risks differ for cancer-specific and non-cancer related mortality.


Subject(s)
Body Mass Index , Comorbidity/trends , Diabetes Mellitus/mortality , Endometrial Neoplasms/complications , Endometrial Neoplasms/mortality , Adolescent , Adult , Aged , Female , Humans , Middle Aged , Risk Factors , Survival Analysis , Young Adult
6.
Br J Cancer ; 113(5): 817-26, 2015 Sep 01.
Article in English | MEDLINE | ID: mdl-26151456

ABSTRACT

BACKGROUND: Observational studies have reported a modest association between obesity and risk of ovarian cancer; however, whether it is also associated with survival and whether this association varies for the different histologic subtypes are not clear. We undertook an international collaborative analysis to assess the association between body mass index (BMI), assessed shortly before diagnosis, progression-free survival (PFS), ovarian cancer-specific survival and overall survival (OS) among women with invasive ovarian cancer. METHODS: We used original data from 21 studies, which included 12 390 women with ovarian carcinoma. We combined study-specific adjusted hazard ratios (HRs) using random-effects models to estimate pooled HRs (pHR). We further explored associations by histologic subtype. RESULTS: Overall, 6715 (54%) deaths occurred during follow-up. A significant OS disadvantage was observed for women who were obese (BMI: 30-34.9, pHR: 1.10 (95% confidence intervals (CIs): 0.99-1.23); BMI: ⩾35, pHR: 1.12 (95% CI: 1.01-1.25)). Results were similar for PFS and ovarian cancer-specific survival. In analyses stratified by histologic subtype, associations were strongest for women with low-grade serous (pHR: 1.12 per 5 kg m(-2)) and endometrioid subtypes (pHR: 1.08 per 5 kg m(-2)), and more modest for the high-grade serous (pHR: 1.04 per 5 kg m(-2)) subtype, but only the association with high-grade serous cancers was significant. CONCLUSIONS: Higher BMI is associated with adverse survival among the majority of women with ovarian cancer.


Subject(s)
Neoplasms, Glandular and Epithelial/pathology , Obesity/pathology , Ovarian Neoplasms/pathology , Body Mass Index , Carcinoma, Ovarian Epithelial , Disease-Free Survival , Female , Humans , Kaplan-Meier Estimate , Neoplasms, Glandular and Epithelial/mortality , Obesity/mortality , Ovarian Neoplasms/mortality
7.
Gynecol Oncol ; 132(3): 566-72, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24368279

ABSTRACT

OBJECTIVE: Folate is essential for DNA synthesis and methylation and is implicated in tumour progression. Few studies have examined its role in ovarian cancer survival. Our objective was to determine relationships between intake of folate, related one-carbon nutrients, single nucleotide polymorphisms (SNPs) in folate-metabolising genes and survival following ovarian cancer diagnosis. METHODS: This analysis included 1270 women with invasive epithelial ovarian cancer diagnosed in 2002-2006. Pre-diagnostic and some post-diagnostic lifestyle, dietary, and sociodemographic information was collected via self-administered questionnaires. DNA samples were genotyped for SNPs in methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTR) and methionine synthase reductase (MTRR) genes. Adjusted hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated using Cox regression. RESULTS: Multivariate analyses did not identify associations between higher pre-diagnostic intake of folate, folic acid, vitamins B2, B6, and B12, methionine, betaine or choline and survival overall. In stratified analyses, higher folic acid and folate intake was associated with significantly worse survival among women with mucinous tumours (HRs per 100 µg 1.30 and 1.43, respectively) and smokers (HRs per 100 µg 1.23 and 1.16 respectively). There was also a suggestion that higher supplemental folic acid use post-diagnosis was associated with worse survival (HR per 100 µg 1.03, 95%CI 1.00-1.05). MTHFR SNP rs2066470 was significantly associated with survival (per allele HR 0.81, 95%CI 0.67-0.98). CONCLUSIONS: Our data provide little evidence that folate intake affects ovarian cancer survival. However, combined effects with smoking, and findings within the mucinous subtype and for post-diagnosis folic acid, warrant further investigation.


Subject(s)
Diet/statistics & numerical data , Folic Acid/administration & dosage , Micronutrients/administration & dosage , Neoplasms, Glandular and Epithelial/mortality , Ovarian Neoplasms/mortality , Aged , Alcohol Drinking/epidemiology , Australia/epidemiology , Carcinoma, Ovarian Epithelial , Case-Control Studies , Cohort Studies , Fallopian Tube Neoplasms/genetics , Fallopian Tube Neoplasms/metabolism , Fallopian Tube Neoplasms/mortality , Fallopian Tube Neoplasms/pathology , Female , Folic Acid/metabolism , Humans , Middle Aged , Multivariate Analysis , Neoplasm Staging , Neoplasms, Glandular and Epithelial/genetics , Neoplasms, Glandular and Epithelial/metabolism , Neoplasms, Glandular and Epithelial/pathology , Ovarian Neoplasms/genetics , Ovarian Neoplasms/metabolism , Ovarian Neoplasms/pathology , Peritoneal Neoplasms/genetics , Peritoneal Neoplasms/metabolism , Peritoneal Neoplasms/mortality , Peritoneal Neoplasms/pathology , Polymorphism, Single Nucleotide , Smoking/epidemiology , Surveys and Questionnaires
8.
Eur J Cancer ; 49(12): 2717-26, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23583438

ABSTRACT

AIM: Obesity is an established risk factor for endometrial cancer. Associations tend to be stronger for the endometrioid subtype. The role of adult weight change and weight cycling is uncertain. Our study aimed to determine whether there is an association between different adult weight trajectories, weight cycling and risk of endometrial cancer overall, and by subtype. METHODS: We analysed data from the Australian National Endometrial Cancer study, a population-based case-control study that collected self-reported information on height, weight at three time points (age 20, maximum and 1 year prior to diagnosis [recent]), intentional weight loss/regain (weight cycling) from 1398 women with endometrial cancer and 1538 controls. Odds ratios (OR) and 95% confidence intervals (CI) were calculated using multivariable logistic regression analysis. RESULTS: Relative to women who maintained a stable weight during adulthood, greater weight gain after the age of 20 was associated with increased risk of endometrial cancer (OR for gain 40+kg all subtypes 5.3, 95% CI 3.9-7.3; endometrioid 6.5, 95% CI 4.7-9.0). The strongest associations were observed among women who were continually overweight from the age of 20 (all subtypes OR 3.6, 95% CI 2.6-5.0). Weight cycling was associated with increased risk, particularly among women who had ever been obese (OR 2.9 95% CI 1.8-4.7), with ~3-fold risks seen for both endometrioid and non-endometrioid tumour subtypes. Women who had intentionally lost weight and maintained that weight loss were not at increased risk. CONCLUSION: These results suggest that higher adult weight gain, and perhaps weight cycling, independently increase the risk of endometrial cancer, however women who lost weight and kept that weight off were not at increased risk.


Subject(s)
Endometrial Neoplasms/physiopathology , Obesity/physiopathology , Weight Gain , Weight Loss , Adolescent , Adult , Aged , Australia , Body Mass Index , Body Weight , Case-Control Studies , Comorbidity , Endometrial Neoplasms/etiology , Female , Humans , Logistic Models , Middle Aged , Multivariate Analysis , Obesity/complications , Risk Assessment , Risk Factors , Young Adult
9.
Cancer Causes Control ; 23(11): 1775-83, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22933054

ABSTRACT

OBJECTIVES: Limited experimental evidence suggests that omega-3 polyunsaturated (n-3) fatty acids inhibit the proliferation of ovarian cancer cells in vitro, whereas omega-6 polyunsaturated (n-6) fatty acids have been shown to promote carcinogenesis, but epidemiological studies to date have been inconclusive. Our aim was to evaluate the role of polyunsaturated fatty acids in ovarian carcinogenesis. METHODS: Participants in the Australian Ovarian Cancer Study (1,366 cases and 1,414 population controls) self-completed risk factor and food frequency questionnaires. Logistic regression models were used to calculate adjusted odds ratio (OR) and 95 % confidence intervals (CI). RESULTS: We found no association between intake of total n-3 fatty acids from foods, or the individual n-3 fatty acids-alpha-linolenic, eicosapentaenoic, docosapentaenoic, docosahexaenoic acids-and ovarian cancer risk. High intake of total n-6 fatty acids was inversely associated with risk (OR for highest vs. lowest category 0.78, 95 % CI 0.60-1.00, p-trend 0.04); however, the association was restricted to n-6 fatty acids from avocado, vegetables, and nuts. Neither higher intake of the individual n-6 fatty acids nor the ratio of n-3 to n-6 fatty acids was associated with ovarian cancer risk. We found no evidence that risk varied by supplement use. CONCLUSIONS: Our data provide no evidence of a protective role for n-3 fatty acids in ovarian carcinogenesis. The benefit, if any, of higher intake of n-6 fatty acids is due to general properties of the food sources, rather than due to the n-6 fatty acids per se.


Subject(s)
Fatty Acids, Omega-3/administration & dosage , Fatty Acids, Omega-6/administration & dosage , Ovarian Neoplasms/epidemiology , Adolescent , Adult , Aged , Australia/epidemiology , Case-Control Studies , Fatty Acids, Omega-3/adverse effects , Fatty Acids, Omega-6/adverse effects , Feeding Behavior , Female , Humans , Middle Aged , Ovarian Neoplasms/etiology , Ovarian Neoplasms/prevention & control , Risk Factors , Surveys and Questionnaires , Young Adult
10.
Eur J Clin Nutr ; 65(10): 1133-40, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21629268

ABSTRACT

BACKGROUND/OBJECTIVE: Folates are essential for DNA synthesis and methylation, and thus may have a role in carcinogenesis. Limited evidence suggests folate-containing foods might protect against some cancers and may partially mitigate the increased risk of breast cancer associated with alcohol intake, but there is little information regarding ovarian cancer. Our aim was to evaluate the role of folate and related micronutrients, polymorphisms in key folate-metabolising genes and environmental factors in ovarian carcinogenesis. SUBJECTS/METHODS: Participants in the Australian Ovarian Cancer Study (1363 cases, 1414 controls) self-completed risk factor and food-frequency questionnaires. DNA samples (1638 cases, 1278 controls) were genotyped for 49 tag single-nucleotide polymorphisms (SNPs) in the methylene tetrahydrofolate reductase (MTHFR), methionine synthase (MTR) and MTR reductase (MTRR) genes. Logistic regression models were used to generate adjusted odds ratios and 95% confidence intervals. RESULTS: We saw no overall association between the intake of folate, B vitamins or other methyl donors and ovarian cancer risk, although increasing folate from foods was associated with reduced risk among current smokers (P(trend)=0.03) and folic acid intake was associated with borderline significant increased risks among women who consumed ≥1 standard alcoholic drinks/day (odds ratio (OR)=1.64; 95% confidence interval (CI) 1.05-2.54, P(trend)=0.05). Two SNPs (rs7365052, rs7526063) showed borderline significant inverse associations with ovarian cancer risk; both had very low minor allele frequencies. There was little evidence for interaction between genotype and micronutrient intake or for variation between different histological subtypes of ovarian cancer. CONCLUSIONS: Our data provide little evidence to support a protective role for folate in ovarian carcinogenesis but suggest further evaluation of the joint effects of folic acid and alcohol is warranted.


Subject(s)
Dietary Supplements , Folic Acid/administration & dosage , Micronutrients/administration & dosage , Ovarian Neoplasms/epidemiology , Ovarian Neoplasms/genetics , 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase/genetics , 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase/metabolism , Adult , Aged , Alcohol Drinking/adverse effects , Alcohol Drinking/genetics , Australia , Case-Control Studies , Diet , Environmental Exposure , Female , Gene Frequency/drug effects , Genotype , Humans , Logistic Models , Methylenetetrahydrofolate Reductase (NADPH2)/genetics , Methylenetetrahydrofolate Reductase (NADPH2)/metabolism , Middle Aged , Odds Ratio , Ovarian Neoplasms/pathology , Polymorphism, Single Nucleotide/drug effects , Risk Factors , Vitamin B Complex/administration & dosage
11.
Ann Oncol ; 22(6): 1332-1338, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21131370

ABSTRACT

BACKGROUND: Our objective was to determine the relationship between dietary glycemic load (GL), glycemic index (GI), carbohydrate intake, and ovarian cancer risk in a population-based case-control study. PATIENTS AND METHODS: A self-administered questionnaire was used to collect data on demographic and lifestyle factors, and a food frequency questionnaire was used to collect dietary information from 1366 women with ovarian cancer and 1414 population controls. RESULTS: GL was positively associated with ovarian cancer. The adjusted odds ratio (OR) for the highest versus the lowest quartile of intake was 1.24 [95% confidence interval (CI) 1.00-1.55, P for trend = 0.03]. Fiber intake was inversely associated with risk. The OR comparing women in the highest fiber-intake group with those in the lowest was 0.78 (95% CI 0.62-0.98, P for trend = 0.11). We found no association between GI, carbohydrate intake, and ovarian cancer. In analyses stratified by body mass index, the risk estimates for GL, carbohydrate, and sugar were higher among overweight/obese women; however, the interaction term was only significant for sugar (P for interaction = 0.004). CONCLUSIONS: Our results suggest that diets with a high GL may increase the risk of ovarian cancer, particularly among overweight/obese women, and a high intake of fiber may provide modest protection.


Subject(s)
Dietary Carbohydrates/adverse effects , Dietary Fiber , Glycemic Index , Ovarian Neoplasms/etiology , Ovarian Neoplasms/pathology , Adult , Aged , Blood Glucose , Body Mass Index , Case-Control Studies , Eating , Female , Humans , Life Style , Middle Aged , Obesity , Ovarian Neoplasms/blood , Risk , Surveys and Questionnaires
12.
Fetal Diagn Ther ; 28(1): 28-33, 2010.
Article in English | MEDLINE | ID: mdl-20693807

ABSTRACT

OBJECTIVES: We report an experimental fetal rat model with the aim of comparing two surgical methods used to check Arnold-Chiari Malformation (ACM) by dysraphism. We also wanted to (1) determine which type(s) of ACM akin to human anatomical findings were generated with the model and (2) study whether a cerebrospinal fluid pressure gradient could be responsible for ACM's etiopathology. MATERIALS AND METHODS: At E20, a mean of two fetuses per pregnant rat underwent an incision at the 2-3 lumbar level, deep into the medulla oblongata central canal, by two different surgical methods. Cesarian section was performed at E22. Dysraphic fetuses were examined clinically. Those born alive and controls without lesions were anatomically and histologically studied. RESULTS: Method 2 was better than method 1 at reproducing the model. 100% of operated fetuses showed no spontaneous motility or sensibility to pressure on the posterior limbs in addition to anatomopathological evidence of type II ACM. CONCLUSIONS: A high rate of ACM could be checked by dysraphism with both methods. The opening of the central canal was demonstrated to generate a cerebrospinal fluid pressure gradient responsible for the herniation of encephalic structures comparable with human ACM. We believe this model may be useful for evaluating further strategies for prenatal treatment.


Subject(s)
Arnold-Chiari Malformation/pathology , Disease Models, Animal , Fetus/pathology , Animals , Arnold-Chiari Malformation/cerebrospinal fluid , Arnold-Chiari Malformation/etiology , Cerebrospinal Fluid Pressure , Female , Fetal Development , Male , Rats , Rats, Sprague-Dawley , Spinal Dysraphism/cerebrospinal fluid , Spinal Dysraphism/pathology
13.
Hum Reprod ; 24(6): 1501-6, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19279040

ABSTRACT

BACKGROUND: Although previous epidemiological studies have shown that women with endometriosis are more likely to be thinner and underweight, it is currently not clear whether this is a true characteristic of women who develop endometriosis or a consequence of their disease and its symptoms. The aim of this study was to investigate the relationship between endometriosis and relative weight in childhood and adolescence, prior to diagnosis. METHODS: This case-control study included 268 Australian women with surgically confirmed moderate to severe endometriosis (cases) and 244 women without endometriosis (controls). Relative weight at ages 10 and 16 years, as recalled and classified ('underweight', 'average weight' and 'overweight') separately by the women themselves and their mothers, was analyzed. RESULTS: Women who reported being overweight at 10 years had an increased risk of endometriosis (OR 2.8; 95% CI 1.1-7.5). Mothers' reports and concordant responses among mother-daughter pairs were consistent with this association. There was no clear evidence of an association between relative weight at 16 years and risk of endometriosis. CONCLUSIONS: These data suggest that being overweight during late childhood is associated with the development of endometriosis; however, the results warrant confirmation in larger study populations.


Subject(s)
Body Weight , Endometriosis/epidemiology , Overweight/epidemiology , Adolescent , Adult , Age Distribution , Australia/epidemiology , Case-Control Studies , Child , Female , Humans , Life Style , Middle Aged , Risk Factors , Severity of Illness Index , Young Adult
14.
BJOG ; 115(3): 339-47, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18190370

ABSTRACT

OBJECTIVE: To evaluate the effectiveness of a decision aid for prenatal testing of fetal abnormalities compared with a pamphlet in supporting women's decision making. DESIGN: A cluster randomised controlled trial. SETTING: Primary health care. POPULATION: Women in early pregnancy consulting a GP. METHODS: GPs were randomised to provide women with either a decision aid or a pamphlet. The decision aid was a 24-page booklet designed using the Ottowa Decision Framework. The pamphlet was an existing resource available in the trial setting. MAIN OUTCOME MEASURES: Validated scales were used to measure the primary outcomes, informed choice and decisional conflict, and the secondary outcomes, anxiety, depression, attitudes to the pregnancy/fetus and acceptability of the resource. Outcomes were measured at 14 weeks of gestation from questionnaires that women completed and returned by post. FINDINGS: Women in the intervention group were more likely to make an informed decision 76% (126/165) than those in the control group 65% (107/165) (adjusted OR 2.08; 95% CI 1.14-3.81). A greater proportion of women in the intervention group 88% (147/167) had a 'good' level of knowledge than those in the control group 72% (123/171) (adjusted OR 3.43; 95% CI 1.79-6.58). Mean (SD) decisional conflict scores were low in both groups, decision aid 1.71 (0.49), pamphlet 1.65 (0.55) (adjusted mean difference 0.10; 95% CI -0.02 to 0.22). There was no strong evidence of differences between the trial arms in the measures of psychological or acceptability outcomes. CONCLUSION: A tailored prenatal testing decision aid plays an important role in improving women's knowledge of first and second trimester screening tests and assisting them to make decisions about screening and diagnostic tests that are consistent with their values.


Subject(s)
Congenital Abnormalities/diagnosis , Decision Making , Decision Support Techniques , Mothers/psychology , Patient Education as Topic/methods , Pregnant Women/psychology , Prenatal Diagnosis/psychology , Adult , Choice Behavior , Congenital Abnormalities/psychology , Family Practice , Female , Humans , Pamphlets , Patient Education as Topic/standards , Pregnancy
15.
Int J Gynecol Cancer ; 18(3): 407-13, 2008.
Article in English | MEDLINE | ID: mdl-17645507

ABSTRACT

Reproductive and hormonal exposures are known to influence ovarian carcinogenesis, but little is known about the effect of these factors on survival. We have studied survival according to hormonal and reproductive history in a population-based cohort of 676 Australian women aged 18-79, newly diagnosed with invasive epithelial ovarian cancer in the early 1990s. In order to place our findings in context, we have also undertaken a systematic review of the pertinent literature. Detailed information about each woman's reproductive and contraceptive history was obtained from pregnancy and contraceptive calendars at the time of diagnosis. Cox regression was used to obtain multivariate adjusted hazard ratios (HR) and 95% confidence intervals (CI). A total of 419 (62%) of the 676 women died during the follow-up (giving a 5-year survival proportion of 44%). Apart from better survival for women who had ever breastfed (multivariate HR 0.74, 95% CI 0.55-0.98), we found no association between survival from invasive ovarian cancer and a range of hormonal and gynecological factors including parity, use of oral contraceptives, and histories of tubal sterilization or hysterectomy. Systematic review of the literature generally supported the lack of influence of these factors on survival from ovarian cancer. We conclude that, except for a possible survival advantage among women with a history of breastfeeding, reproductive and hormonal exposures prior to diagnosis do not influence survival from invasive ovarian cancer, in contrast to their substantial effects on etiology of this disease.


Subject(s)
Contraceptives, Oral, Hormonal/administration & dosage , Neoplasms, Glandular and Epithelial/mortality , Neoplasms, Glandular and Epithelial/pathology , Ovarian Neoplasms/mortality , Ovarian Neoplasms/pathology , Reproductive History , Adolescent , Adult , Age Distribution , Aged , Case-Control Studies , Cohort Studies , Confidence Intervals , Contraceptives, Oral, Hormonal/adverse effects , Disease-Free Survival , Female , Humans , Immunohistochemistry , Middle Aged , Neoplasm Staging , Neoplasms, Glandular and Epithelial/therapy , Ovarian Neoplasms/therapy , Parity , Pregnancy , Probability , Prognosis , Queensland/epidemiology , Risk Factors , Survival Analysis
16.
Rev. neurol. (Ed. impr.) ; 33(7): 624-627, 1 oct., 2001.
Article in Es | IBECS | ID: ibc-27220

ABSTRACT

Introducción. El test de denominación de Boston (TDB) es una de las pruebas más frecuentemente utilizadas para evaluar la denominación en pacientes con enfermedad de Alzheimer. Debido a su longitud, se han desarrollado varias formas abreviadas de esta prueba. Objetivo. El propósito de este estudio fue crear una versión abreviada del TDB en español que permita detectar los cambios semánticos precoces en la enfermedad de Alzheimer. Pacientes y métodos. Se han estudiado 103 pacientes con enfermedad de Alzheimer probable (criterios NINCDS-ADRDA), con GDS< 5, y 143 sujetos sanos, apareados por edad y escolaridad. Fueron excluidos aquellos sujetos con antecedentes de alcoholismo, otras enfermedades neurológicas o psiquiátricas previas y con educación <4 años. Pacientes y controles fueron evaluados con una batería neuropsicológica completa, que incluyó la versión de 60 láminas del TDB en español (adaptación Buenos Aires). Se calculó la sensibilidad y especificidad de cada lámina y su variabilidad con los datos demográficos. Se seleccionaron las 12 láminas más sensibles y específicas, y con menor variabilidad respecto a edad y escolaridad. Para el análisis estadístico se utilizó el análisis de varianza (ANOVA) y el coeficiente de correlación de Spearman. Resultados. La media del desempeño de los controles en la versión de 12 ítems fue de 11 puntos, con un desvío estándar de 1,16. No se observó correlación con edad (r= 0,14574) ni con el nivel educacional (r= 0,101293). La sensibilidad y especificidad para el diagnóstico de EA fue del 85 y 94 por ciento, respectivamente, similar a los valores de la versión original. Conclusión. Esta versión reducida de 12 ítems del TDB en español constituye una herramienta neuropsicológica útil para la detección de la EA, ya que conserva la capacidad discriminativa de la versión original, y no presenta influencia demográfica (AU)


Subject(s)
Middle Aged , Aged , Aged, 80 and over , Humans , Neuropsychological Tests , Sensitivity and Specificity , Statistics , Analysis of Variance , Alzheimer Disease
18.
Rev Neurol ; 33(7): 624-7, 2001.
Article in Spanish | MEDLINE | ID: mdl-11784949

ABSTRACT

INTRODUCTION: The Boston Naming Test (BNT) is the most frequently used test of confrontation naming. Due to its length, several abbreviated forms have been proposed. OBJECTIVE: The aim of the study was to develop a short form for the Spanish version of the BNT that could detect early semantic changes in Alzheimer s disease (AD). PATIENTS AND METHODS: One hundred and three patients with diagnosis of probable AD (NINCDS ADRDA criteria), with GDS< 5 and 143 normal subjects, matched for age and education, were studied. Subjects with <4 years of education were excluded. No subject had any history of neurological of psychiatric disorders or alcohol abuse. All participants underwent a comprehensive neuropsychological assessment which included the 60 item Spanish version of the BNT. The sensibility and specificity of each item and demographic effect s variability were calculated (ANOVA). Those 12 figures with the highest sensibility and specificity which showed no significant educational or age variation were administered to all participants. The Spearman correlation coefficient was used. RESULTS: Mean score for the control group was 11 (standard deviation: 1.16). No significant effects for age (r= 0.14574) or education (r= 0.101293) were found. The sensibility and specificity for correctly diagnosing AD was 85% and 94% respectively, similar to the longest version. CONCLUSION: This 12 item version of the BNT can be a useful instrument for a rapid screening of AD, as it is as sensible and specific as the 60 item version, and it is not influenced by age or education.


Subject(s)
Alzheimer Disease/diagnosis , Neuropsychological Tests , Aged , Aged, 80 and over , Alzheimer Disease/physiopathology , Analysis of Variance , Humans , Middle Aged , Neuropsychological Tests/standards , Sensitivity and Specificity , Statistics as Topic
19.
Am J Perinatol ; 17(5): 225-8, 2000.
Article in English | MEDLINE | ID: mdl-11110337

ABSTRACT

The role of the Neonatal Nurse Practitioner has been evolving since the early 1970s. The original concept and design was born out of individual hospital's needs for highly professional and skilled personnel at the bedside. Thus, initial programs were hospital-based and granted certificates. Over the past 20 years, a gradual shift toward graduate degrees and standardization of programs has been seen. The role and responsibilities of the neonatal nurse practitioner have also expanded over that time period. From their strictly clinical beginnings, neonatal nurse practitioners now contribute to research, nursing and medical education, and administration. This article looks at the neonatal nurse practitioner role and the impact that education and legislation have had on its evolution.


Subject(s)
Intensive Care Units, Neonatal , Neonatal Nursing , Nurse Practitioners , Humans , Infant, Newborn , Nurse Practitioners/statistics & numerical data
20.
Actas esp. psiquiatr ; 28(6): 373-378, nov. 2000.
Article in Es | IBECS | ID: ibc-1808

ABSTRACT

Introducción: Los sujetos que envejecen se 'quejan' de sus olvidos, los cuales pueden ser normales o el síntoma de inicio de la enfermedad de Alzheimer. El objetivo del presente trabajo fue estudiar en controles normales, en sujetos con deterioro de memoria asociado a la edad (DAME) y en pacientes con Demencia de tipo Alzheimer (DTA) la importancia de esta queja, el reporte de su familiar y el rendimiento en las baterías objetivas de memoria. Material y método: 73 pacientes (41 DMAE; y 32 DTA) y 30 controles fueron evaluados con un Cuestionario de Memoria Subjetiva, una Batería Objetiva de Memoria y la Escala de Depresión de Hamilton. Resultados: La queja es significativamente mayor en los sujetos con DMAE. La queja de los pacientes no se correlacionó con la edad, la escolaridad, el sexo, el MMSE ni con las pruebas objetivas de memoria pero sí con la escala de depresión de Hamilton. El cuestionario completado por el familiar correlaciona con las pruebas de memoria pero no con la escala de depresión del paciente. Conclusiones: Estos resultados responderían a los rasgos ansioso-depresivos en los controles y DMAE o a la anosognosia en los pacientes dementes. El reporte familiar es el mejor predictor del rendimiento mnésico del paciente (AU)


Subject(s)
Aged , Male , Female , Humans , Memory , Surveys and Questionnaires , Alzheimer Disease , Family
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