42 research outputs found
Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer.
While elevated blood cholesterol has been associated with an increased risk of colorectal cancer (CRC) in observational studies, causality is uncertain. Here we apply a Mendelian randomisation (MR) analysis to examine the potential causal relationship between lipid traits and CRC risk. We used single nucleotide polymorphisms (SNPs) associated with blood levels of total cholesterol (TC), triglyceride (TG), low-density lipoprotein (LDL), and high-density lipoprotein (HDL) as instrumental variables (IV). We calculated MR estimates for each risk factor with CRC using SNP-CRC associations from 9,254 cases and 18,386 controls. Genetically predicted higher TC was associated with an elevated risk of CRC (odds ratios (OR) per unit SD increase = 1.46, 95% confidence interval [CI]: 1.20-1.79, P=1.68x10−4). The pooled ORs for LDL, HDL, and TG were 1.05 (95% CI: 0.92-1.18, P=0.49), 0.94 (95% CI: 0.84-1.05, P= 0.27), and 0.98 (95% CI: 0.85-1.12, P=0.75) respectively. A genetic risk score for 3-hydoxy-3-methylglutaryl-coenzyme A reductase (HMGCR) to mimic the effects of statin therapy was associated with a reduced CRC risk (OR=0.69, 95% CI: 0.49-0.99, P=0.046). This study supports a causal relationship between higher levels of TC with CRC risk, and a further rationale for implementing public health strategies to reduce the prevalence of hyperlipidaemia. This article is protected by copyright. All rights reserved
The Glanville fritillary genome retains ancient karyotype and reveals selective chromosomal fusions in Lepidoptera
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Association between suicidal behaviour and impaired glucose metabolism in depressive disorders
Genome sequencing and population genomic analyses provide insights into the adaptive landscape of silver birch
Silver birch (Betula pendula) is a pioneer boreal tree that can be induced to flower within 1 year. Its rapid life cycle, small (440-Mb) genome, and advanced germplasm resources make birch an attractive model for forest biotechnology. We assembled and chromosomally anchored the nuclear genome of an inbred B. pendula individual. Gene duplicates from the paleohexaploid event were enriched for transcriptional regulation, whereas tandem duplicates were overrepresented by environmental responses. Population resequencing of 80 individuals showed effective population size crashes at major points of climatic upheaval. Selective sweeps were enriched among polyploid duplicates encoding key developmental and physiological triggering functions, suggesting that local adaptation has tuned the timing of and cross-talk between fundamental plant processes. Variation around the tightly-linked light response genes PHYC and FRS10 correlated with latitude and longitude and temperature, and with precipitation for PHYC. Similar associations characterized the growth-promoting cytokinin response regulator ARR1, and the wood development genes KAK and MED5A.Peer reviewe
Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease
To identify new risk loci for colorectal cancer (CRC), we conducted a meta-analysis of seven genome-wide association studies (GWAS) with independent replication, totalling 13 656 CRC cases and 21 667 controls of European ancestry. The combined analysis identified a new risk association for CRC at 2q35 marked by rs992157 (P = 3.15 x 10(-8), odds ratio = 1.10, 95% confidence interval = 1.06-1.13), which is intronic to PNKD (paroxysmal non-kinesigenic dyskinesia) and TMBIM1 (transmembrane BAX inhibitor motif containing 1). Intriguingly this susceptibility single-nucleotide polymorphism (SNP) is in strong linkage disequilibrium (r(2) = 0.90, D' = 0.96) with the previously discovered GWAS SNP rs2382817 for inflammatory bowel disease (IBD). Following on from this observation we examined for pleiotropy, or shared genetic susceptibility, between CRC and the 200 established IBD risk loci, identifying an additional 11 significant associations (false discovery rate [FDR]) <0.05). Our findings provide further insight into the biological basis of inherited genetic susceptibility to CRC, and identify risk factors that may influence the development of both CRC and IBD.Peer reviewe
Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer
Background: Observational studies have associated adiposity with an increased risk of colorectal cancer (CRC). However, such studies do not establish a causal relationship. To minimise bias from confounding we performed a Mendelian randomisation (MR) analysis to examine the relationship between adiposity and CRC. Methods: We used SNPs associated with adult body mass index (BMI), waist-hip ratio (WHR), childhood obesity and birth weight as instrumental variables in a MR analysis of 9254 CRC cases and 18 386 controls. Results: In the MR analysis, the odds ratios (ORs) of CRC risk per unit increase in BMI, WHR and childhood obesity were 1.23 (95% CI: 1.02-1.49, P = 0.033), 1.59 (95% CI: 1.08-2.34, P = 0.019) and 1.07 (95% CI: 1.03-1.13, P = 0.018), respectively. There was no evidence for association between birth weight and CRC (OR = 1.22, 95% CI: 0.89-1.67, P = 0.22). Combining these data with a concurrent MR-based analysis for BMI and WHR with CRC risk (totalling to 18 190 cases, 27 617 controls) provided increased support, ORs for BMI and WHR were 1.26 (95% CI: 1.10-1.44, P = 7.7 x 10(-4)) and 1.40 (95% CI: 1.14-1.72, P = 1.2 x 10(-3)), respectively. Conclusions: These data provide further evidence for a strong causal relationship between adiposity and the risk of developing CRC highlighting the urgent need for prevention and treatment of adiposity.Peer reviewe
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Author Correction: Genome sequencing and population genomic analyses provide insights into the adaptive landscape of silver birch.
In the version of this article initially published, there was a mistake in the calculation of the nucleotide mutation rate per site per generation: 1 × 10−9 mutations per site per generation was used, whereas 9.5 × 10−9 was correct. This error affects the interpretation of population-size changes over time and their possible correspondence with known geological events, as shown in the original Fig. 4 and supporting discussion in the text, as well as details in the Supplementary Note. Neither the data themselves nor any other results are affected. Figure 4 has been revised accordingly. Images of the original and corrected figure panels are shown in the correction notice
Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes
Genome-wide association studies (GWAS) have identified more than 200 common genetic variants independently associated with colorectal cancer (CRC) risk, but the causal variants and target genes are mostly unknown. We sought to fine-map all known CRC risk loci using GWAS data from 100,204 cases and 154,587 controls of East Asian and European ancestry. Our stepwise conditional analyses revealed 238 independent association signals of CRC risk, each with a set of credible causal variants (CCVs), of which 28 signals had a single CCV. Our cis-eQTL/mQTL and colocalization analyses using colorectal tissue-specific transcriptome and methylome data separately from 1299 and 321 individuals, along with functional genomic investigation, uncovered 136 putative CRC susceptibility genes, including 56 genes not previously reported. Analyses of single-cell RNA-seq data from colorectal tissues revealed 17 putative CRC susceptibility genes with distinct expression patterns in specific cell types. Analyses of whole exome sequencing data provided additional support for several target genes identified in this study as CRC susceptibility genes. Enrichment analyses of the 136 genes uncover pathways not previously linked to CRC risk. Our study substantially expanded association signals for CRC and provided additional insight into the biological mechanisms underlying CRC development
A computational study to estimate the possibilities to improve utilisation of stainless steelmaking slags
Abstract
Utilisation of solidified AOD slags from stainless steelmaking is hindered by dicalcium silicate, which causes disintegration and dusting of solidified slag. Utilisation of AOD slags may be improved by changing the slag composition to the composition range in which dicalcium silicate is not formed. Instead of changing the composition during the AOD process — which is not favourable for the process optimization — it is possible to mix AOD slag with other slags in order to obtain compositions more suitable for slag utilisation and hence improve the material efficiency of stainless steelmaking. Integration of ferrochrome and stainless steel production in the Outokumpu Tornio plant enables the mixing of AOD slags with submerged arc furnace (SAF) slags before the slags are solidified. In addition to changing the slag composition to the composition range that favours its utilisation, the combination of two slags enables the reduction of chromium from both slags with a single treatment. Without the recovery of chromium, the chromium losses would be significant especially with the SAF slags. The purpose of this study was to study the behaviour of the slag systems in which AOD and SAF slags are mixed with different ratios. Firstly, the phase compositions of different slag compositions in different temperatures were evaluated. Secondly, reduction of chromium from different slag systems using coke, methane and ferrosilicon as reductants was evaluated in a constant temperature. According to the results the formation of dicalcium silicate is avoided if the amount of SAF slag is more than 30 %. However, the liquidus temperature of the slag mixture increases with increasing SAF slag -content, which defines an upper limit for the amount of SAF slag. Chromium can be reduced from the slag mixtures with all the considered reductants, although the amounts of reductants required for reduction varied greatly
Magnetic preconcentration and process mineralogical study of the Kiviniemi Sc-enriched ferrodiorite
Abstract
Scandium is classified as a critical raw material by the European Union. Its beneficiation from various primary and secondary sources is currently being studied under several research and development projects. Due to the geochemical characteristics of Sc, its enrichment to ore grades by geological processes is scarce. Potential new sources are investigated to respond to the expected increasing demand for this rare earth metal. The recently discovered Kiviniemi Sc deposit in Finland represents an igneous occurrence with estimated total resources of 13.4 Mt and an average Sc grade of 163 g/t. The deposit consists of relatively homogeneous ferrodioritic intrusive body with its main unit with ~2.5 ha surface extension. Scandium is mainly incorporated into the lattice of clinopyroxene and amphibole within the main unit. Composite samples from three drill cores from various parts of the main unit were concentrated with a combination of low-intensity and high-gradient magnetic separation. Depending on the feed characteristics, high-gradient magnetic separation reached recoveries between 87% and 92% with 230–310 ppm Sc while removing 35–49 mass percent of gangue minerals, mainly plagioclase and potassium feldspar. Our study provides information on the magnetic preconcentration conditions with process mineralogical details and produced concentrates for further testing according to the suggested processing scheme