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  • Ovid Technologies (Wolters Kluwer Health)  (15)
  • 1
    In: Obstetrical & Gynecological Survey, Ovid Technologies (Wolters Kluwer Health), Vol. 70, No. 12 ( 2015-12), p. 758-762
    Type of Medium: Online Resource
    ISSN: 0029-7828
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2015
    detail.hit.zdb_id: 2043471-6
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  • 2
    In: Menopause, Ovid Technologies (Wolters Kluwer Health), Vol. 29, No. 3 ( 2022-01-10), p. 293-303
    Abstract: Oral postmenopausal hormone therapy (HT) has been shown to be associated with venous thromboembolism (VTE), but whether this association is modified by VTE-associated genetic susceptibility is unknown. We examined interactions between oral HT use and a genetic risk score (GRS) of VTE. Method: Eligible women were postmenopausal women who had data on oral HT use, VTE incidence between 1990 and 2012, and genetic data in the Nurses’ Health Study. We built a GRS aggregating 16 VTE-related genetic variants. We used Cox regression to estimate associations of HT use with incident VTE and assessed interactions between HT use and VTE GRS. We also estimated incidence of VTE between age 50 and 79 years for groups of women defined by HT use and VTE GRS. Results: We identified 432 incident VTE cases. Current HT users were at higher risk of VTE than never users (HR: 1.9, 95% CI: 1.5-2.6), with slightly higher risk for estrogen plus progestin HT than estrogen only (HR: 2.4 vs 1.9). The GRS was associated with VTE risk (HR comparing 4th quartile to 1st: 2.0, 95% CI: 1.2-3.4). We did not observe significant multiplicative interactions between HT use and GRS. The estimated VTE risk difference (per 10,000 person-years) comparing 50-year-old current HT users to never users was 22.5 for women in the highest GRS quartile and 9.8 for women in the lowest GRS quartile. Conclusion: The VTE GRS might inform clinical guidance regarding the balance of risks and benefits of HT use, especially among younger women.
    Type of Medium: Online Resource
    ISSN: 1530-0374
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2022
    detail.hit.zdb_id: 2071114-1
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  • 3
    In: The Journal of Urology, Ovid Technologies (Wolters Kluwer Health), Vol. 181, No. 4 ( 2009-4), p. 643-
    Type of Medium: Online Resource
    ISSN: 0022-5347
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2009
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  • 4
    In: Circulation, Ovid Technologies (Wolters Kluwer Health), Vol. 141, No. Suppl_1 ( 2020-03-03)
    Abstract: Air pollution exposure is an important risk factor for cardiovascular morbidity and mortality. Acute exposure is associated with episodes of atrial fibrillation (AF), and long-term exposure may influence ventricular mass and volume. However, little is understood about the relationship between long-term pollution exposure and atrial structure and function, which may influence risk of AF and heart failure. We sought to determine the association of long-term exposure to oxides of nitrogen (NO X ), particulate matter smaller than 2.5 micrometers (PM 2.5 ), and ozone (O 3 ) with left atrial structure (LA) and function, as measured by LA volume, emptying fraction, and peak longitudinal strain. In the Multi-Ethnic Study of Atherosclerosis (MESA), a longitudinal study of 6,814 participants in six United States communities, we used estimated 5-year average exposure to PM 2.5 , NO X , and O 3 prior to outcome measurement from validated hierarchical spatio-temporal models developed from extensive monitoring of MESA participants. Left atrial measures were calculated from cardiac magnetic resonance imaging occurring between 2010 and 2012. Linear regression was used, adjusting for MESA study site and potential confounding characteristics. In 2,250 MESA participants, 5-year average exposure to PM 2.5 , NO X , and O 3 varied greatly by study site and was not associated with LA volume, emptying fraction, or peak longitudinal strain. Results were particularly sensitive to adjustment for study site, suggesting that there was substantial unmeasured confounding by US city/region. Using recently developed study-specific exposure estimation and highly accurate imaging, we did not find evidence to suggest an association between long-term exposure to several common pollutants and measures of left atrial structure and function. Additional analyses in areas of higher pollution may be useful in determining whether associations are consistent across exposure levels.
    Type of Medium: Online Resource
    ISSN: 0009-7322 , 1524-4539
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2020
    detail.hit.zdb_id: 1466401-X
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  • 5
    In: JAIDS Journal of Acquired Immune Deficiency Syndromes, Ovid Technologies (Wolters Kluwer Health), Vol. 86, No. 3 ( 2021-03-1), p. 339-343
    Abstract: Evaluate differences in weight change by regimen among people living with HIV (PLWH) initiating antiretroviral therapy (ART) in the current era. Methods: Between 2012 and 2019, 3232 ART-naïve PLWH initiated ≥3-drug ART regimens in 8 Centers for AIDS Research Network of Integrated Clinical Systems sites. We estimated weight change by regimen for 11 regimens in the immediate (first 6 months) and extended (all follow-up on initial regimen) periods using linear mixed models adjusted for time on regimen, interaction between time and regimen, age, sex, race/ethnicity, hepatitis B/C coinfection, nadir CD4, smoking, diabetes, antipsychotic medication, and site. We included more recently approved regimens [eg, with tenofovir alafenamide fumarate (TAF)] only in the immediate period analyses to ensure comparable follow-up time. Results: Mean follow-up was 1.9 years on initial ART regimen. In comparison to efavirenz/tenofovir disoproxil fumarate (TDF)/emtricitabine (FTC), initiating bictegravir/TAF/FTC {3.9 kg [95% confidence interval (CI): 2.2 to 5.5]} and dolutegravir/TAF/FTC [4.4 kg (95% CI: 2.1 to 6.6)] were associated with the greatest weight gain in the immediate period, followed by darunavir/TDF/FTC [3.7 kg (95% CI: 2.1 to 5.2)] and dolutegravir/TDF/FTC [2.6 kg (95% CI: 1.3 to 3.9)] . In the extended period, compared with efavirenz/TDF/FTC, initiating darunavir/TDF/FTC was associated with a 1.0 kg (95% CI: 0.5 to 1.5) per 6-months greater weight gain, whereas dolutegravir/abacavir/FTC was associated with a 0.6-kg (95% CI: 0.3 to 0.9) and dolutegravir/TDF/FTC was associated with a 0.6-kg (95% CI: 0.1 to 1.1) per 6-months greater gain. Weight gain on dolutegravir/abacavir/FTC and darunavir/TDF/FTC was significantly greater than that for several integrase inhibitor-based regimens. Conclusions: There is heterogeneity between regimens in weight gain following ART initiation among previously ART-naïve PLWH; we observed greater gain among PLWH taking newer integrase strand transfer inhibitors (DTG, BIC) and DRV-based regimens.
    Type of Medium: Online Resource
    ISSN: 1525-4135
    RVK:
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2021
    detail.hit.zdb_id: 2038673-4
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  • 6
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2011
    In:  Epidemiology Vol. 22, No. 6 ( 2011-11), p. 813-814
    In: Epidemiology, Ovid Technologies (Wolters Kluwer Health), Vol. 22, No. 6 ( 2011-11), p. 813-814
    Type of Medium: Online Resource
    ISSN: 1044-3983
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2011
    detail.hit.zdb_id: 2042095-X
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  • 7
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2018
    In:  Journal of the American Heart Association Vol. 7, No. 22 ( 2018-11-20)
    In: Journal of the American Heart Association, Ovid Technologies (Wolters Kluwer Health), Vol. 7, No. 22 ( 2018-11-20)
    Abstract: Venous thromboembolism ( VTE ) is a complex thrombotic disorder that constitutes a major source of mortality and morbidity. To improve understanding of the cause of VTE , we conducted a metabolomic analysis in a case‐control study including 240 incident VTE cases and 6963 controls nested within 3 large prospective population‐based cohorts, the Nurses’ Health Study, the Nurses’ Health Study II , and the Health Professionals Follow‐Up Study. Methods and Results For each individual, we measured 211 metabolites and collected detailed information on lifestyle factors. We performed logistic regression and enrichment analysis to identify metabolites and biological categories associated with incident VTE risk, accounting for key confounders, such as age, sex, smoking, alcohol consumption, body mass index, and comorbid diseases (eg, cancers). We performed analyses of all VTEs and separate analyses of pulmonary embolism. Using the basic model controlling for age, sex, and primary disease, we identified 60 nominally significant VTE ‐ or pulmonary embolism–associated metabolites ( P 〈 0.05). These metabolites were enriched for diacylglycerols ( P permutation 〈 0.05). However, after controlling for multiple testing, only 1 metabolite (C5 carnitine; odds ratio, 1.25; 95% confidence interval, 1.10–1.41; P corrected =0.03) remained significantly associated with VTE . After further adjustment for body mass index, no metabolites were significantly associated with disease after accounting for multiple testing, and no metabolite classes were enriched for nominally significant associations. Conclusions Although our findings suggest that circulating metabolites may influence the risk of incident VTE , the associations we observed were confounded by body mass index. Larger studies involving additional individuals and with broader metabolomics coverage are needed to confirm our findings.
    Type of Medium: Online Resource
    ISSN: 2047-9980
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2018
    detail.hit.zdb_id: 2653953-6
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  • 8
    In: Circulation, Ovid Technologies (Wolters Kluwer Health), Vol. 135, No. suppl_1 ( 2017-03-07)
    Abstract: Introduction: Moderate alcohol consumption has been associated with differences in hemostatic factor levels that may lead to a lower thrombotic risk, but the association between alcohol consumption and the risk of incident pulmonary embolism (PE) has been inconsistent. Hypotheses: Moderate alcohol consumption is associated with a lower PE risk than lower or higher quantities, and more frequent alcohol consumption is associated with a lower PE risk than less frequent alcohol consumption. Methods: Nurses’ Health Study participants free of venous thromboembolism in 1984 (n=79,914) reported alcohol consumption every two-four years between 1984 and 2012 and number of drinking days per week on five questionnaires between 1986 and 2004. PE were initially identified by self-report and were confirmed for the subset of patients without a previous cancer using a combination of medical record review and participant reconfirmation. Cox Proportional Hazards models estimated multivariable-adjusted hazard ratios for PE associated with average amount of alcohol consumed and, separately, drinking days per week. Secondary analyses estimated the risk of medical-record confirmed idiopathic PE, events which were not associated with surgery, trauma, or cancer. Results: We identified 1,112 total incident PE events, including 360 idiopathic PE events, during 28 years of follow-up. In multivariable-adjusted analyses, we found no strong evidence of an association between the amount of alcohol consumed per day and the risk of any PE (quadratic p-trend=0.3) or idiopathic PE (quadratic p-trend=0.4) or between the frequency of alcohol consumption and the risk of any PE (linear p-trend=0.5) or idiopathic PE (linear p-trend=0.8) (Table). Conclusions: Among this population of women with relatively low average amounts of alcohol consumption, we found no substantial evidence of an association between the amount or frequency of alcohol consumption and the risk of PE.
    Type of Medium: Online Resource
    ISSN: 0009-7322 , 1524-4539
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2017
    detail.hit.zdb_id: 1466401-X
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  • 9
    In: Circulation: Genomic and Precision Medicine, Ovid Technologies (Wolters Kluwer Health), Vol. 12, No. 12 ( 2019-12)
    Abstract: Evidence from randomized trials has shown that therapies that lower LDL (low-density lipoprotein)-cholesterol and triglycerides reduce coronary artery disease (CAD) risk. However, there is still uncertainty about their effects on other cardiovascular outcomes. We therefore performed a systematic investigation of causal relationships between circulating lipids and cardiovascular outcomes using a Mendelian randomization approach. Methods: In the primary analysis, we performed 2-sample multivariable Mendelian randomization using data from participants of European ancestry. We also conducted univariable analyses using inverse-variance weighted and robust methods, and gene-specific analyses using variants that can be considered as proxies for specific lipid-lowering medications. We obtained associations with lipid fractions from the Global Lipids Genetics Consortium, a meta-analysis of 188 577 participants, and genetic associations with cardiovascular outcomes from 367 703 participants in UK Biobank. Results: For LDL-cholesterol, in addition to the expected positive associations with CAD risk (odds ratio [OR] per 1 SD increase, 1.45 [95% CI, 1.35–1.57] ) and other atheromatous outcomes (ischemic cerebrovascular disease and peripheral vascular disease), we found independent associations of genetically predicted LDL-cholesterol with abdominal aortic aneurysm (OR, 1.75 [95% CI, 1.40–2.17]) and aortic valve stenosis (OR, 1.46 [95% CI, 1.25–1.70] ). Genetically predicted triglyceride levels were positively associated with CAD (OR, 1.25 [95% CI, 1.12–1.40]), aortic valve stenosis (OR, 1.29 [95% CI, 1.04–1.61] ), and hypertension (OR, 1.17 [95% CI, 1.07–1.27]), but inversely associated with venous thromboembolism (OR, 0.79 [95% CI, 0.67–0.93] ) and hemorrhagic stroke (OR, 0.78 [95% CI, 0.62–0.98]). We also found positive associations of genetically predicted LDL-cholesterol and triglycerides with heart failure that appeared to be mediated by CAD. Conclusions: Lowering LDL-cholesterol is likely to prevent abdominal aortic aneurysm and aortic stenosis, in addition to CAD and other atheromatous cardiovascular outcomes. Lowering triglycerides is likely to prevent CAD and aortic valve stenosis but may increase thromboembolic risk.
    Type of Medium: Online Resource
    ISSN: 2574-8300
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2019
    detail.hit.zdb_id: 2927603-2
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  • 10
    In: Menopause, Ovid Technologies (Wolters Kluwer Health), Vol. 24, No. 2 ( 2017-02), p. 150-156
    Abstract: Several attributes of female reproductive history, including age at natural menopause (ANM), have been related to primary open-angle glaucoma (POAG). We assembled 18 previously reported common genetic variants that predict ANM to determine their association with ANM or POAG. Methods: Using data from the Nurses’ Health Study (7,143 women), we validated the ANM weighted genetic risk score in relation to self-reported ANM. Subsequently, to assess the relation with POAG, we used data from 2,160 female POAG cases and 29,110 controls in the National Eye Institute Glaucoma Human Genetics Collaboration Heritable Overall Operational Database (NEIGHBORHOOD), which consists of 8 datasets with imputed genotypes to 5.6+ million markers. Associations with POAG were assessed in each dataset, and site-specific results were meta-analyzed using the inverse weighted variance method. Results: The genetic risk score was associated with self-reported ANM ( P  = 2.2 × 10 –77 ) and predicted 4.8% of the variance in ANM. The ANM genetic risk score was not associated with POAG (Odds Ratio (OR) = 1.002; 95% Confidence Interval (CI): 0.998, 1.007; P  = 0.28). No single genetic variant in the panel achieved nominal association with POAG ( P ≥0.20). Compared to the middle 80 percent, there was also no association with the lowest 10 th percentile or highest 90 th percentile of genetic risk score with POAG (OR = 0.75; 95% CI: 0.47, 1.21; P  = 0.23 and OR = 1.10; 95% CI: 0.72, 1.69; P  = 0.65, respectively). Conclusions: A genetic risk score predicting 4.8% of ANM variation was not related to POAG; thus, genetic determinants of ANM are unlikely to explain the previously reported association between the two phenotypes.
    Type of Medium: Online Resource
    ISSN: 1072-3714 , 1530-0374
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2017
    detail.hit.zdb_id: 2071114-1
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