Publications by authors named "Dron J"

Bromobenzoquinones and 2,4,6-tribromophenol belong to disinfection or chlorination by-products than can be formed in bromide-rich waters during chlorination or chloramination. Due to their high toxicities, sensitive and cost-effective analytical methods are necessary to detect and quantify them in various environmental matrices. A determination method of 2,5-dibromo-1,4-benzoquinone, 2,6-dibromo-3,5-dimethyl-1,4-benzoquinone, 2,6-dibromo-3-chloro-5-methyl-1,4-benzoquinone, 2,3,5,6-tetrabromo-1,4-benzoquinone and, 2,4,6-tribromophenol was developed using solid-phase extraction and electron capture detector-gas chromatography separation and detection (SPE-GC-ECD).

View Article and Find Full Text PDF

The determination of 18 metals and metalloids was realized in 4 tissues of 62 Stenella coeruleoalba specimens stranded along the French Mediterranean coastline from 2010 to 2016. While most concentrations were comparable to mean worldwide levels, Hg levels were alarming (1190 μg g dw, in average). The results were discussed together with previous measurements in the same area, from 2002 to 2009.

View Article and Find Full Text PDF

Purpose Of Review: This review highlights contributions of the Global Lipids Genetics Consortium (GLGC) in advancing the understanding of the genetic etiology of blood lipid traits, including total cholesterol, LDL cholesterol, HDL cholesterol, triglycerides, and non-HDL cholesterol. We emphasize the consortium's collaborative efforts, discoveries related to lipid and lipoprotein biology, methodological advancements, and utilization in areas extending beyond lipid research.

Recent Findings: The GLGC has identified over 923 genomic loci associated with lipid traits through genome-wide association studies (GWASs), involving more than 1.

View Article and Find Full Text PDF

The extensive use of pesticides combined with their persistence in the environment requires new methodologies to assess more effectively the population exposure to pesticides via air pollution. Biomonitoring pesticides with lichens has been poorly documented, although it represents a complementary approach to the usual active samplings, with an exposure to pesticides accumulated and integrated over several months. An optimized extraction procedure from the lichen Xanthoria parietina followed by a gas chromatographic-tandem mass spectrometric analysis is proposed here to quantify simultaneously 48 pesticides considered in France as priority active substances to monitor in the air.

View Article and Find Full Text PDF
Article Synopsis
  • This study identifies and characterizes rare coding alleles linked to genetic dyslipidemia, a major risk factor for coronary artery disease, using data from over 1.1 million individuals across various ancestries.
  • It discovered 800 significant variants across 209 genes, with a notable focus on non-European populations, and included a diverse cohort of participants to enhance genetic understanding.
  • The findings highlight potential therapeutic targets, particularly new genes that may help lower LDL cholesterol levels, providing valuable insights for future genetic disease research and drug development.
View Article and Find Full Text PDF
Article Synopsis
  • - The study investigates the link between insulin resistance and various metabolic diseases, emphasizing the need to consider insulin resistance in epidemiological studies.
  • - By analyzing genetic data from over 382,000 individuals, researchers identified 251 genetic loci related to insulin resistance and prioritized key genes through further analysis.
  • - Notable findings include genes like PLA2G12A and PLA2G6, which enhance insulin sensitivity, and TNFAIP8, which affects insulin resistance differently in females by increasing fat accumulation; these could be potential biomarkers or drug targets.
View Article and Find Full Text PDF

Background: Arterial and venous cardiovascular conditions, such as coronary artery disease (CAD), peripheral artery disease (PAD), and venous thromboembolism (VTE), are genetically correlated. Interrogating underlying mechanisms may shed light on disease mechanisms. In this study, we aimed to identify (1) epidemiological and (2) causal, genetic relationships between metabolites and CAD, PAD, and VTE.

View Article and Find Full Text PDF
Article Synopsis
  • Heterozygous familial hypercholesterolemia (HeFH) is a genetic condition that leads to high cholesterol and increased heart disease risk, though individuals show varying levels of risk for developing coronary artery disease (CAD).
  • This study analyzed 1,315 HeFH carriers and their matched noncarrier relatives in the Netherlands, along with data from 151,009 participants in the UK Biobank, to investigate how common DNA variants affect CAD risk through a polygenic score.
  • Results demonstrated that HeFH individuals had higher CAD rates than noncarriers, and that a higher polygenic score significantly increased CAD risk, sometimes to levels seen in noncarriers, highlighting the role of genetic factors
View Article and Find Full Text PDF

Background: Dyslipoproteinemia often involves simultaneous derangements of multiple lipid traits. We aimed to evaluate the phenotypic and genetic characteristics of combined lipid disturbances in a general population-based cohort.

Methods: Among UK Biobank participants without prevalent coronary artery disease, we used blood lipid and apolipoprotein B concentrations to ascribe individuals into 1 of 6 reproducible and mutually exclusive dyslipoproteinemia subtypes.

View Article and Find Full Text PDF

Previous studies found lipid levels, especially triglycerides (TG), are associated with acute pancreatitis, but their causalities and bi-directions were not fully examined. We determined whether abnormal levels of TG, high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C) are precursors and/or consequences of acute pancreatitis using bidirectional two-sample Mendelian randomization (MR) with two non-overlapping genome-wide association study (GWAS) summary statistics for lipid levels and acute pancreatitis. We found phenotypic associations that both higher TG levels and lower HDL-C levels contributed to increased risk of acute pancreatitis.

View Article and Find Full Text PDF
Article Synopsis
  • Familial hypercholesterolemia (FH) is a genetic condition linked to high LDL cholesterol levels and increased risk of early coronary heart disease (CHD), though its effects on CHD in those with moderate LDL-C levels are not fully understood.
  • * This study evaluated the CHD risk from FH variants in individuals with both moderately and severely elevated LDL-C levels and estimated the additional deaths from CHD related to FH in U.S. adults.
  • * Among 21,426 participants, those with FH variants had significantly higher rates of developing CHD, with hazard ratios of 2.9 for those with moderately elevated LDL-C and 2.6 for those with severely elevated LDL-C.
View Article and Find Full Text PDF
Article Synopsis
  • Hypertensive disorders of pregnancy (HDPs), such as gestational hypertension and preeclampsia, significantly increase risks of maternal health issues and long-term cardiovascular disease across the globe.
  • The study aimed to link specific proteins in the blood to HDPs using genetic data, employing two-sample mendelian randomization for analysis.
  • Findings involved a broad dataset, including over 393,000 women for gestational hypertension and nearly 607,000 for preeclampsia, uncovering associations between 90 candidate cardiovascular-related proteins and these hypertensive disorders.
View Article and Find Full Text PDF

Rationale: Arterial and venous cardiovascular conditions, such as coronary artery disease (CAD), peripheral artery disease (PAD), and venous thromboembolism (VTE), are genetically correlated. Interrogating distinct and overlapping mechanisms may shed new light on disease mechanisms.

Objective: In this study, we aimed to: identify and compare (1) epidemiologic and (2) causal, genetic relationships between metabolites and CAD, PAD, and VTE.

View Article and Find Full Text PDF
Article Synopsis
  • * Individuals with extreme traits or high risk for serious diseases are more effectively identified through a small number of rare variants rather than through numerous common variants that have minimal effects.
  • * By integrating rare variants from related genes into a single genetic risk model, we created a more effective tool for predicting disease risk across different populations, outperforming traditional methods based on common variants.
View Article and Find Full Text PDF
Article Synopsis
  • * Rare mutations in certain genes have a much stronger impact on severe diseases than more common genetic variations.
  • * By using rare variants to create a genetic risk model, we were able to predict disease risk more effectively across different populations compared to traditional methods that rely on common variants.
View Article and Find Full Text PDF

There are few cetacean tissue-specific polycyclic aromatic hydrocarbon (PAH) concentration studies in the Mediterranean, despite this region is among the most subjected to chemical contamination. PAH analyses were conducted in different tissues of striped dolphins (Stenella coeruleoalba, N = 64) and bottlenose dolphins (Tursiops truncatus, N = 9) stranded along the French Mediterranean coastline from 2010 to 2016. Comparable levels were measured in S.

View Article and Find Full Text PDF

For the return of polygenic risk scores to become an acceptable clinical practice in psychiatry, receipt of polygenic risk scores must be associated with minimal harm and changes in behavior that decrease one's risk for developing a psychiatric outcome. Data from a randomized controlled trial was used to assess the impact of different levels of hypothetical polygenic risk scores for alcohol use disorder on psychological distress, risk perception, and intentions to change drinking behaviors. The analytic sample consisted of 325 participants recruited from an urban, public university.

View Article and Find Full Text PDF

Importance: Protein-truncating variants (PTVs) in apolipoprotein B (APOB) and proprotein convertase subtilisin/kexin type 9 (PCSK9) are associated with significantly lower low-density lipoprotein (LDL) cholesterol concentrations. The association of these PTVs with coronary heart disease (CHD) warrants further characterization in large, multiracial prospective cohort studies.

Objective: To evaluate the association of PTVs in APOB and PCSK9 with LDL cholesterol concentrations and CHD risk.

View Article and Find Full Text PDF

Purpose Of Review: Combined hyperlipidemia is the most common lipid disorder and is strongly polygenic. Given its prevalence and associated risk for atherosclerotic cardiovascular disease, this review describes the potential for utilizing polygenic risk scores for risk prediction and management of combined hyperlipidemia.

Recent Findings: Different diagnostic criteria have led to inconsistent prevalence estimates and missed diagnoses.

View Article and Find Full Text PDF

Introduction: As gene identification efforts have advanced in psychiatry, so have aspirations to use genome-wide polygenic information for prevention and intervention. Although polygenic risk scores (PRS) for substance use and psychiatric outcomes are not yet available in clinical settings, individuals can access their PRS through online direct-to-consumer resources. One of these widely used websites reports that alcohol use disorder is the third most requested PRS out of >1,000 conditions.

View Article and Find Full Text PDF

Background: Biallelic pathogenic variants in lipoprotein lipase (LPL) cause familial chylomicronemia syndrome with severe hypertriglyceridemia (HTG), defined as plasma triglycerides (TG) > 10 mmol/L (> 885 mg/dL). TG levels in individuals with one copy of a pathogenic LPL gene variant is less familiar; some assume that the phenotype is intermediate between homozygotes and controls.

Objective: We undertook an evaluation of the longitudinal TG phenotype of individuals heterozygous for pathogenic LPL variants.

View Article and Find Full Text PDF

Objectives: We show that participatory research approaches can be a useful tool across disciplines and data collection methods to explore the socio-exposome near one of the largest industrial harbors in Europe. We analyzed resident involvement in each project and their capacity to affect structural changes.

Methods: Longitudinal participatory environmental monitoring studies on lichens, petunias, aquatic systems and groundwater were conducted under the program VOCE (Volunteers for the Citizens' Observation of the Environment), which mobilized nearly 100 volunteers to collect and report data.

View Article and Find Full Text PDF

Background: A familial predisposition to sudden and/or arrhythmic death (SAD) in the setting of coronary artery disease (CAD) exists; however, the genetic basis is poorly understood.

Objectives: The purpose of this study was to determine whether a genome-wide polygenic score for coronary artery disease (GPS) might have utility in SAD risk stratification in CAD patients without severe systolic dysfunction.

Methods: A previously validated GPS was generated utilizing genome-wide genotyping in 4,698 PRE-DETERMINE participants of European ancestry with CAD and left ventricular ejection fraction >30%-35%.

View Article and Find Full Text PDF

2,4,6-tribromophenol (TBP) is implied in the production of brominated flame retardants but is also a major chlorination by-product in seawater. A growing number of studies indicate that TBP is highly toxic to the marine biota, but the contribution of anthropogenic sources among natural production is still under question concerning its bioaccumulation in marine organisms. Here, several water sampling campaigns were carried out in the industrialized Gulf of Fos (northwestern Mediterranean Sea, France) and clearly showed the predominant incidence of industrial chlorination discharges on the TBP levels in water, at the 1-10 ng L level in average and reaching up to 580 ng L near the outlets.

View Article and Find Full Text PDF