Characterization and transitions of asphalt cement composite materials

Blends of a PG 64-22 asphalt with a range of load levels (0.2 — 20 wt %) of Sasobit® wax and a single loading of 2 wt % Elvaloy AM® were prepared and characterized. Sasobit® wax is a high molecular weight paraffinic wax produced commercially through the Fischer-Tropsch process. Elvaloy AM® is a reactive elastic terpolymer, comprised of ethylene, butyl acrylate and glycidyl methacrylate monomeric units. The blends were analyzed by gel permeation chromatography (GPC), differential scanning calorimetry (DSC), x-ray diffraction, epifluorescence microscopy, scanning laser confocal microscopy, and dynamic shear rheology. Sasobit (1 wt %) composite material showed little difference in aging characteristics with respect to the aging chromatograms of the un-modified asphalt cement. Aging of Elvaloy (2 wt %) composite material leads to increased concentrations of asphaltene and asphaltene aggregate components at a greater rate than that observed with the Sasobit composites and unmodified asphalt cement. Analysis of DSC heating curve enthalpies revealed that Sasobit composites at loadings above 4% that the Sasobit was completely crystalline. X-ray diffraction confirmed that ambient temperature Sasobit composite samples maintained their crystalline form down to the level of 0.2 wt % loading. Evidence for the additives presence could be seen within the asphalt matrix through epifluorescence and scanning laser confocal microscopy imaging of each of the composite systems investigated. Bright point-sources of fluorescence, most easily picked out in the Elvaloy (2 wt %) composite images, are believed to be asphaltene micelles. Evidence of improved G* performance in both Sasobit and Elvaloy composite master curves with respect to the neat asphalt cement master curves is presented. The dynamic viscosity data at 1 Hz shows that original and TFOT data doesn’t clearly differentiate between Sasobit composites and neat asphalt cement until after PAV aging. At that stage the Sasobit composite shows truly linear dynamic viscosity response suggesting that Sasobit inclusion leads to better dispersion of the viscosity building asphaltene component throughout the asphalt cement. It is believed that the Elvaloy AM composite experienced some degree of crosslinking during aging and this is most evident following the PAV aging in the rheological data

Rainfall interception and redistribution by a common North American understory and pasture forb, \u3cem\u3eEupatorium capillifolium\u3c/em\u3e (Lam. dogfennel)

In vegetated landscapes, rain must pass through plant canopies and litter to enter soils. As a result, some rainwater is returned to the atmosphere (i.e., interception, I) and the remainder is partitioned into a canopy (and gap) drip flux (i.e., throughfall) or drained down the stem (i.e., stemflow). Current theoretical and numerical modeling frameworks for this process are almost exclusively based on data from woody overstory plants. However, herbaceous plants often populate the understory and are the primary cover for important ecosystems (e.g., grasslands and croplands). This study investigates how overstory throughfall (PT,o) is partitioned into understory I, throughfall (PT) and stemflow (PS) by a dominant forb in disturbed urban forests (as well as grasslands and pasturelands), Eupatorium capillifolium (Lam., dogfennel). Dogfennel density at the site was 56 770 stems ha−1, enabling water storage capacities for leaves and stems of 0.90±0.04 and 0.43±0.02 mm, respectively. As direct measurement of PT,o (using methods such as tipping buckets or bottles) would remove PT,o or disturb the understory partitioning of PT,o, overstory throughfall was modeled (PT,o′ role= presentation \u3eP′T,o) using on-site observations of PT,o from a previous field campaign. Relying on modeled PT,o′ role= presentation \u3eP′T,o, rather than on observations of PT,o directly above individual plants means that significant uncertainty remains with respect to (i) small-scale relative values of PT and PS and (ii) factors driving PS variability among individual dogfennel plants. Indeed, PS data from individual plants were highly skewed, where the mean PS:PT,o′ role= presentation \u3ePS:P′T,o per plant was 36.8 %, but the median was 7.6 % (2.8 %–27.2 % interquartile range) and the total over the study period was 7.9 %. PS variability (n=30 plants) was high (CV \u3e 200 %) and may hypothetically be explained by fine-scale spatiotemporal patterns in actual overstory throughfall (as no plant structural factors explained the variability). The total PT:PT,o′ role= presentation \u3ePT:P′T,o was 71 % (median PT:PT,o′ role= presentation \u3ePT:P′T,o per gauge was 72 %, with a 59 %–91 % interquartile range). Occult precipitation (mixed dew and light rain events) occurred during the study period, revealing that dogfennel can capture and drain dew to their stem base as PS. Dew-induced PS may help explain dogfennel\u27s improved invasion efficacy during droughts (as it tends to be one of the most problematic weeds in the improved grazing systems in the southeastern US). Overall, dogfennel\u27s precipitation partitioning differed markedly from the site\u27s overstory trees (Pinus palustris), and a discussion of the limited literature suggests that these differences may exist across vegetated ecosystems. Thus, more research on herbaceous plant canopy interactions with precipitation is merited

Telomere structure and maintenance gene variants and risk of five cancer types.

Telomeres cap chromosome ends, protecting them from degradation, double-strand breaks, and end-to-end fusions. Telomeres are maintained by telomerase, a reverse transcriptase encoded by TERT, and an RNA template encoded by TERC. Loci in the TERT and adjoining CLPTM1L region are associated with risk of multiple cancers. We therefore investigated associations between variants in 22 telomere structure and maintenance gene regions and colorectal, breast, prostate, ovarian, and lung cancer risk. We performed subset-based meta-analyses of 204,993 directly-measured and imputed SNPs among 61,851 cancer cases and 74,457 controls of European descent. Independent associations for SNP minor alleles were identified using sequential conditional analysis (with gene-level p value cutoffs ≤3.08 × 10-5 ). Of the thirteen independent SNPs observed to be associated with cancer risk, novel findings were observed for seven loci. Across the DCLRE1B region, rs974494 and rs12144215 were inversely associated with prostate and lung cancers, and colorectal, breast, and prostate cancers, respectively. Across the TERC region, rs75316749 was positively associated with colorectal, breast, ovarian, and lung cancers. Across the DCLRE1B region, rs974404 and rs12144215 were inversely associated with prostate and lung cancers, and colorectal, breast, and prostate cancers, respectively. Near POT1, rs116895242 was inversely associated with colorectal, ovarian, and lung cancers, and RTEL1 rs34978822 was inversely associated with prostate and lung cancers. The complex association patterns in telomere-related genes across cancer types may provide insight into mechanisms through which telomere dysfunction in different tissues influences cancer risk.Funding for the iCOGS infrastructure came from: the European Community’s Seventh Framework Programme under grant agreement n° 223175 (HEALTH-F2-2009-223175) (COGS), Cancer Research UK (C1287/A10118, C1287/A 10710, C12292/A11174, C1281/A12014, C5047/A8384, C5047/A15007, C5047/A10692, C8197/A16565), the National Institutes of Health (CA128978) and Post-Cancer GWAS initiative (1U19 CA148537, 1U19 CA148065 and 1U19 CA148112 – the GAME-ON initiative), the Department of Defense (W81XWH-10-1-0341), the Canadian Institutes of Health Research (CIHR) for the CIHR Team in Familial Risks of Breast Cancer, Komen Foundation for the Cure, the Breast Cancer Research Foundation, and the Ovarian Cancer Research Fund.This is the author accepted manuscript. The final version is available from Wiley via http://dx.doi.org/10.1002/ijc.3028

Novel Common Genetic Susceptibility Loci for Colorectal Cancer

BACKGROUND: Previous genome-wide association studies (GWAS) have identified 42 loci (P < 5 × 10-8) associated with risk of colorectal cancer (CRC). Expanded consortium efforts facilitating the discovery of additional susceptibility loci may capture unexplained familial risk. METHODS: We conducted a GWAS in European descent CRC cases and control subjects using a discovery-replication design, followed by examination of novel findings in a multiethnic sample (cumulative n = 163 315). In the discovery stage (36 948 case subjects/30 864 control subjects), we identified genetic variants with a minor allele frequency of 1% or greater associated with risk of CRC using logistic regression followed by a fixed-effects inverse variance weighted meta-analysis. All novel independent variants reaching genome-wide statistical significance (two-sided P < 5 × 10-8) were tested for replication in separate European ancestry samples (12 952 case subjects/48 383 control subjects). Next, we examined the generalizability of discovered variants in East Asians, African Americans, and Hispanics (12 085 case subjects/22 083 control subjects). Finally, we examined the contributions of novel risk variants to familial relative risk and examined the prediction capabilities of a polygenic risk score. All statistical tests were two-sided. RESULTS: The discovery GWAS identified 11 variants associated with CRC at P < 5 × 10-8, of which nine (at 4q22.2/5p15.33/5p13.1/6p21.31/6p12.1/10q11.23/12q24.21/16q24.1/20q13.13) independently replicated at a P value of less than .05. Multiethnic follow-up supported the generalizability of discovery findings. These results demonstrated a 14.7% increase in familial relative risk explained by common risk alleles from 10.3% (95% confidence interval [CI] = 7.9% to 13.7%; known variants) to 11.9% (95% CI = 9.2% to 15.5%; known and novel variants). A polygenic risk score identified 4.3% of the population at an odds ratio for developing CRC of at least 2.0. CONCLUSIONS: This study provides insight into the architecture of common genetic variation contributing to CRC etiology and improves risk prediction for individualized screenin

Effect of angiotensin-converting enzyme inhibitor and angiotensin receptor blocker initiation on organ support-free days in patients hospitalized with COVID-19

IMPORTANCE Overactivation of the renin-angiotensin system (RAS) may contribute to poor clinical outcomes in patients with COVID-19. Objective To determine whether angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) initiation improves outcomes in patients hospitalized for COVID-19. DESIGN, SETTING, AND PARTICIPANTS In an ongoing, adaptive platform randomized clinical trial, 721 critically ill and 58 non–critically ill hospitalized adults were randomized to receive an RAS inhibitor or control between March 16, 2021, and February 25, 2022, at 69 sites in 7 countries (final follow-up on June 1, 2022). INTERVENTIONS Patients were randomized to receive open-label initiation of an ACE inhibitor (n = 257), ARB (n = 248), ARB in combination with DMX-200 (a chemokine receptor-2 inhibitor; n = 10), or no RAS inhibitor (control; n = 264) for up to 10 days. MAIN OUTCOMES AND MEASURES The primary outcome was organ support–free days, a composite of hospital survival and days alive without cardiovascular or respiratory organ support through 21 days. The primary analysis was a bayesian cumulative logistic model. Odds ratios (ORs) greater than 1 represent improved outcomes. RESULTS On February 25, 2022, enrollment was discontinued due to safety concerns. Among 679 critically ill patients with available primary outcome data, the median age was 56 years and 239 participants (35.2%) were women. Median (IQR) organ support–free days among critically ill patients was 10 (–1 to 16) in the ACE inhibitor group (n = 231), 8 (–1 to 17) in the ARB group (n = 217), and 12 (0 to 17) in the control group (n = 231) (median adjusted odds ratios of 0.77 [95% bayesian credible interval, 0.58-1.06] for improvement for ACE inhibitor and 0.76 [95% credible interval, 0.56-1.05] for ARB compared with control). The posterior probabilities that ACE inhibitors and ARBs worsened organ support–free days compared with control were 94.9% and 95.4%, respectively. Hospital survival occurred in 166 of 231 critically ill participants (71.9%) in the ACE inhibitor group, 152 of 217 (70.0%) in the ARB group, and 182 of 231 (78.8%) in the control group (posterior probabilities that ACE inhibitor and ARB worsened hospital survival compared with control were 95.3% and 98.1%, respectively). CONCLUSIONS AND RELEVANCE In this trial, among critically ill adults with COVID-19, initiation of an ACE inhibitor or ARB did not improve, and likely worsened, clinical outcomes. TRIAL REGISTRATION ClinicalTrials.gov Identifier: NCT0273570