Publications by authors named "Ronald Glabonjat"

Importance: Metals are established neurotoxicants, but evidence of their association with cognitive performance at low chronic exposure levels is limited.

Objective: To investigate the association of urinary metal levels, individually and as a mixture, with cognitive tests and dementia diagnosis, including effect modification by apolipoprotein ε4 allele (APOE4).

Design, Setting, And Participants: The multicenter prospective cohort Multi-Ethnic Study of Atherosclerosis (MESA) was started from July 2000 to August 2002, with follow-up through 2018.

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Article Synopsis
  • A study investigated the link between urinary metal levels (both nonessential and essential) and the progression of coronary artery calcium (CAC), a marker for cardiovascular disease, in participants from the Multi-Ethnic Study of Atherosclerosis (MESA).
  • Results showed that higher levels of metals like cadmium, tungsten, uranium, and cobalt were associated with significantly increased CAC levels over 10 years, indicating a potential risk factor for cardiovascular disease.
  • The findings suggest that exposure to certain metals has a comparable impact on coronary calcification as traditional cardiovascular risk factors, emphasizing the need for further research into environmental influences on heart health.
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Arsenic is a ubiquitous toxic metalloid causing serious health problems. Speciation analysis of arsenic in human urine provides valuable insights for large-scale epidemiological studies and informs on sources of exposure as well as human metabolism. The Multi-Ethnic Study of Atherosclerosis (MESA) is a valuable cohort for assessing chronic low-moderate arsenic exposure and health effects in an ethnically diverse US population.

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  • Selenium is a crucial nutrient that can have negative health effects at both low and high levels, prompting research into how it affects DNA methylation and related diseases in a specific population (American Indians).
  • In a study involving 1,357 participants, researchers measured urinary selenium levels and conducted DNA methylation analysis, identifying five key CpG sites significantly associated with these levels.
  • The results showed only minor changes in DNA methylation linked to urinary selenium, indicating that its health impacts might involve mechanisms beyond just DNA methylation alterations.
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  • - This study examined how exposure to various metals in urine relates to cardiovascular disease (CVD) and overall mortality, involving a diverse group of 6,599 U.S. adults over nearly two decades.
  • - Researchers found significant links between higher urinary levels of metals like cadmium, copper, and uranium and increased risks for developing CVD and higher all-cause mortality rates.
  • - Specifically, those in the highest quartile of metal exposure had up to 1.68 times greater risk of all-cause mortality compared to those with the lowest levels, highlighting a concerning relationship between metal exposure and health outcomes.
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Background: Inorganic arsenic is metabolized to monomethyl- (MMAs) and dimethyl- (DMAs) species via one-carbon metabolism (OCM); this facilitates urinary arsenic elimination. OCM is influenced by folate and vitamin B12 and previous randomized control trials (RCTs) showed that folic acid (FA) supplementation increases arsenic methylation in adults. This RCT investigated the effects of FA + B12 supplementation on arsenic methylation in children, a key developmental stage where OCM supports growth.

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Background: More than 700 million people worldwide suffer from diseases of the pancreas, such as diabetes, pancreatitis and pancreatic cancer. Often dysregulation of potassium (K) channels, co-transporters and pumps can promote development and progression of many types of these diseases. The role of K transport system in pancreatic cell homeostasis and disease development remains largely unexplored.

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Background: Chronic arsenic exposure has been associated with an increased risk of cardiovascular disease; diabetes; cancers of the lung, pancreas and prostate; and all-cause mortality in American Indian communities in the Strong Heart Study.

Objective: The Strong Heart Water Study (SHWS) designed and evaluated a multilevel, community-led arsenic mitigation program to reduce arsenic exposure among private well users in partnership with Northern Great Plains American Indian Nations.

Methods: A cluster randomized controlled trial (cRCT) was conducted to evaluate the effectiveness of the SHWS arsenic mitigation program over a 2-y period on ) urinary arsenic, and ) reported use of arsenic-safe water for drinking and cooking.

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  • The analysis of trace elements in urine is an important method for evaluating exposures to harmful substances, nutritional health, and directing public health efforts, particularly using samples from the Multi-Ethnic Study of Atherosclerosis (MESA).
  • This study presents a highly sensitive method for detecting 18 trace elements in just 100 μL of urine, utilizing inductively coupled plasma mass spectrometry (ICP-MS), with good accuracy and varying precision levels across elements.
  • Findings reveal the concentration patterns of non-essential and essential trace elements in urine, with non-essential elements like strontium and arsenic being more prevalent than essential ones like zinc and selenium among MESA participants.
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  • - The study explores the link between urinary metal levels and cardiovascular disease (CVD) by analyzing data from 6,418 participants over a ten-year period, focusing on non-essential metals like cadmium and essential metals such as cobalt and zinc.
  • - Results showed that higher urinary levels of cadmium, tungsten, uranium, and cobalt were significantly associated with increased coronary artery calcium (CAC) progression, indicating a higher risk of atherosclerotic CVD over time.
  • - While cadmium had a strong association with both baseline and ten-year follow-up measures of CAC, the effect of copper and zinc diminished after adjusting for clinical risk factors, suggesting varying impacts of different metals on cardiovascular health.
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  • Chronic exposure to inorganic arsenic (As) and uranium (U) in the U.S. primarily comes from private wells and community water systems, with assumptions that their contribution to total exposure is low when concentrations are low.
  • The study investigated how much these water sources contributed to urinary biomarkers in American Indian and diverse urban communities, analyzing data from over 8,000 participants.
  • Results indicated that both As and U levels in urine significantly increased with higher concentrations of these contaminants in the water, highlighting their substantial impact on internal exposure to these harmful substances.
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Gold nanoparticles (AuNPs) are useful tools for noninvasive drug delivery. AuNP nebulization has shown poor deposition results, and AuNP tracking postadministration has involved methods inapplicable to clinical settings. The authors propose an intratracheal delivery method for minimal AuNP loss and computed tomography scans for noninvasive tracking.

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Klebsiella spp. that secrete the DNA-alkylating enterotoxin tilimycin colonize the human intestinal tract. Numbers of toxigenic bacteria increase during antibiotic use, and the resulting accumulation of tilimycin in the intestinal lumen damages the epithelium via genetic instability and apoptosis.

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Background: Epigenetic dysregulation has been proposed as a key mechanism for arsenic-related cardiovascular disease (CVD). We evaluated differentially methylated positions (DMPs) as potential mediators on the association between arsenic and CVD.

Methods: Blood DNA methylation was measured in 2321 participants (mean age 56.

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Background: Arsenic hydrocarbons, major arsenolipids occurring naturally in marine fish, have substantial cytotoxicity leading to human health-related studies of their distribution and abundance in foods. These studies have all investigated fresh foods; because most fish are cooked before being consumed, it is both food- and health-relevant to determine the arsenolipids present in cooked fish.

Methods: We used HPLC/mass spectrometry to investigate the arsenolipids present in salmon (Salmo salar) before and after cooking by either baking or steaming.

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Despite a recent increase in e-cigarette use, the adverse human health effects of exposure to e-cigarette aerosol, especially on the central nervous system (CNS), remain unclear. Multiple neurotoxic metals have been identified in e-cigarette aerosol. However, it is unknown whether those metals accumulate in the CNS at biologically meaningful levels.

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Arsenic-containing hydrocarbons (AsHCs) are common constituents of marine organisms and have potential toxicity to human health. This work is to study the effect of AsHCs on long-term potentiation (LTP) for the first time. A multi-electrode array (MEA) system was used to record the field excitatory postsynaptic potential (fEPSP) of CA1 before and after treatment with AsHC 360 in hippocampal slices from infantile male rats.

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Although the natural occurrence of arsenic-containing lipids (arsenolipids) in marine organisms is now well established, the possible role of these unusual compounds in organisms and in the cycling of arsenic in marine systems remains largely unexplored. We report the finding of arsenolipids in 61 plankton samples collected from surface marine waters of high- and low-nutrient content along a transect spanning the Gulf Stream in the North Atlantic Ocean. Using high-performance liquid chromatography (HPLC) coupled to both elemental and molecular mass spectrometry, we show that all 61 plankton samples contained six identifiable arsenolipids, namely, three arsenosugar phospholipids (AsPL958, 10-13%; AsPL978, 13-25%; and AsPL1006, 7-10% of total arsenolipids), two arsenic-containing hydrocarbons (AsHC332, 4-10% and AsHC360, 1-2%), and a methoxy-sugar arsenolipid that contained phytol (AsSugPhytol, 1-3%).

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The naturally occurring selenoneine (SeN), the selenium analogue of the sulfur-containing antioxidant ergothioneine, can be found in high abundance in several marine fish species. However, data on biological properties of SeN and its relevance for human health are still scarce. This study aims to investigate the transfer and presystemic metabolism of SeN in a well-established in vitro model of the blood-brain barrier (BBB).

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Although enzymes have been found for many reactions, there are still transformations for which no enzyme is known. For instance, not a single defined enzyme has been described for the reduction of the C=N bond of an oxime, only whole organisms. Such an enzymatic reduction of an oxime may give access to (chiral) amines.

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The As concentrations, along with 34 other elements, and the As speciation were investigated in wild-grown samples of the parasitic mushroom Tolypocladium ophioglossoides with inductively coupled plasma mass spectrometry (ICPMS) and high performance liquid chromatography coupled to ICPMS. The As concentrations were 0.070-3.

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Non-ribosomal peptides are one class of bacterial metabolites formed by gut microbiota. Intestinal resident Klebsiella oxytoca produces two pyrrolobenzodiazepines, tilivalline and tilimycin, via the same nonribosomal biosynthesis platform. These molecules cause human disease by genotoxic and tubulin inhibitory activities resulting in apoptosis of the intestinal epithelium, loss of barrier integrity and ultimately colitis.

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Primary production in Mono Lake, a hypersaline soda lake rich in dissolved inorganic arsenic, is dominated by strain ML. We set out to determine if this photoautotrophic picoplankter could metabolize inorganic arsenic and in doing so form unusual arsenolipids (e.g.

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Arsenolipids include a wide range of organic arsenic species that occur naturally in seafood and thereby contribute to human arsenic exposure. Recently arsenic-containing phosphatidylcholines (AsPCs) were identified in caviar, fish, and algae. In this first toxicological assessment of AsPCs, we investigated the stability of both the oxo- and thioxo-form of an AsPC under experimental conditions, and analyzed cell viability, indicators of genotoxicity and biotransformation in human liver cancer cells (HepG2).

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