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Article ; Online: Improved Specificity of Glutamate Decarboxylase 65 Autoantibody Measurement Using Luciferase-Based Immunoprecipitation System Assays.

Wyatt, Rebecca C / Grace, Sian L / Brigatti, Cristina / Marzinotto, Ilaria / Gillard, Ben T / Shoemark, Deborah K / Chandler, Kyla / Achenbach, Peter / Piemonti, Lorenzo / Long, Anna E / Gillespie, Kathleen M / Lampasona, Vito / Williams, Alistair J K

Diabetes

2024 Volume 73, Issue 4, Page(s) 565–571

MeSH term(s)	Humans ; Diabetes Mellitus, Type 1 ; Glutamate Decarboxylase ; Sensitivity and Specificity ; Autoantibodies ; Luciferases/genetics ; Immunoprecipitation
Chemical Substances	Glutamate Decarboxylase (EC 4.1.1.15) ; Autoantibodies ; Luciferases (EC 1.13.12.-)
Language	English
Publishing date	2024-01-17
Publishing country	United States
Document type	Journal Article
ZDB-ID	80085-5
ISSN	1939-327X ; 0012-1797
ISSN (online)	1939-327X
ISSN	0012-1797
DOI	10.2337/db23-0550
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Article ; Online: The preanalytical stability of emerging cannabinoid analogs (delta-8 THC and its metabolites, delta-10 THC and carboxy-HHC) in urine.

Pokhai, Ashley A / Poklis, Justin L / Williams, Grace R / Wolf, Carl E

Journal of analytical toxicology

2023 Volume 47, Issue 8, Page(s) 726–731

Abstract: There has been a surge in the presence and use of cannabinoids since the federal legalization of hemp (Agricultural Improvement Act of 2018). This increase is attributed not only to the use of ∆9-tetrahydrocannabinol (∆9-THC) and cannabidiol, the most ... ...

Abstract	There has been a surge in the presence and use of cannabinoids since the federal legalization of hemp (Agricultural Improvement Act of 2018). This increase is attributed not only to the use of ∆9-tetrahydrocannabinol (∆9-THC) and cannabidiol, the most abundant phytocannabinoid components of cannabis and hemp, respectively, but also to the use of many other emerging THC analogs. Structurally, these analogs are similar to ∆9-THC. Urine specimens for drug analysis are often collected offsite and transported to a laboratory for analysis. Screening assays are usually the first step in urine drug testing. These assays are usually qualitative and automated, which for negative specimens, reduce cost and reporting time. The stability of ∆9-THC and its metabolites has been known for some time; however, the stability of emerging analogs has not been elucidated, and therefore, assuming equivalent storage stability can be erroneous. Previous work assessed the cross-reactivity of ∆8-THC and its major metabolites, the ∆10-THC chiral analogs and the chiral 11-COOH-hexahydrocannabinol analogs. Stability was assessed for each analyte at a concentration two times greater than the analytes' determined decision point. Samples were prepared in drug-free urine at three different pHs (4.5, 7 and 9) and stored at three different temperatures (4°C, 20°C and 45°C) in triplicate. Samples were analyzed utilizing the Lin-Zhi International Cannabinoids Enzyme Immunoassay cannabinoid screening kit calibrated at the 25 ng/mL cut-off. Overall, the cannabinoid analogs produced diminishing instrument responses depending on pH and temperature. The parent analogs were not detected after a single day at 45°C regardless of pH. In general, carboxylic acid analogs at the acidic pH (4.5) produced diminished instrument responses when compared to their counterparts stored at neutral (7) and basic (9) pH. The time, storage temperature and pH of urine specimens may affect the screening results of specimens collected for cannabinoid drug screening.
MeSH term(s)	Cannabinoids/urine ; Dronabinol ; Hallucinogens/urine ; Cannabidiol ; Cannabis
Chemical Substances	Cannabinoids ; Dronabinol (7J8897W37S) ; Hallucinogens ; Cannabidiol (19GBJ60SN5)
Language	English
Publishing date	2023-08-24
Publishing country	England
Document type	Journal Article
ZDB-ID	752391-9
ISSN	1945-2403 ; 0146-4760
ISSN (online)	1945-2403
ISSN	0146-4760
DOI	10.1093/jat/bkad061
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Article ; Online: The cross-reactivity of cannabinoid analogs (delta-8-THC, delta-10-THC and CBD), their metabolites and chiral carboxy HHC metabolites in urine of six commercially available homogeneous immunoassays.

Wolf, Carl E / Pokhai, Ashley A / Poklis, Justin L / Williams, Grace R

Journal of analytical toxicology

2023 Volume 47, Issue 8, Page(s) 732–736

Abstract: There has been an exponential surge in the presence and use of cannabinoids since the federal legalization of hemp (Agricultural Improvement Act of 2018). This growth is attributed to delta-9-tetrahydrocannabinol (delta-9-THC) and cannabidiol (CBD), the ... ...

Abstract	There has been an exponential surge in the presence and use of cannabinoids since the federal legalization of hemp (Agricultural Improvement Act of 2018). This growth is attributed to delta-9-tetrahydrocannabinol (delta-9-THC) and cannabidiol (CBD), the most abundant phytocannabinoid components of cannabis and hemp, respectively, but with many other emerging THC analogs. Structurally, these analogs are similar to delta-9-THC, yet very little information is available about their potency and even less information is available regarding their detectability using commercially available cannabinoid screening kits. Due to their structural similarity, current cannabinoid homogeneous immunoassay screening methods may be able to detect these emerging cannabinoid analogs and their metabolites. Six urine immunoassay kits (Abbott Cannabinoids-Abbott Diagnostics, LZI Cannabinoids (cTHC) Enzyme Immunoassay-Lin-Zhi International, DRI® Cannabinoid Assay and CEDIA™ THC-Thermo Fisher Scientific, ONLINE DAT Cannabinoid II-Roche Diagnostics and Syva EMIT®II Plus-Siemens Healthineers) were evaluated at two different cutoff concentrations: 50 ng/mL and 20 or 25 ng/mL, assay dependent. The analysis was performed on an Abbott Architect Plus c4000 (Abbott Diagnostics). Delta-8-THC, CBD, olivetol and their major metabolites, and delta-10-THC and HHC carboxylic acid chiral analogs were evaluated. The cross-reactivity was evaluated by preparing each analyte at 20, 50, 100 and 1,000 ng/mL in urine. Analytes that did not cross-react at 1,000 ng/mL for a cutoff were considered not detectable. If detected, the lowest concentration was used as the decision point to determine the precision at the immunoassay's cutoff. The six commercially available urine cannabinoid homogeneous immunoassay screening kits cross reacted with the following analogs: delta-8-THC, 11-OH-delta-8-THC, 11-COOH-delta-8-THC, 6-OH-CBD, 7-OH-CBD, all delta-10-THC and HHC carboxylic acid chiral analogs and olivetol with varying selectivity depending on the screening kit and cutoff concentration. The kits did not cross-react with the following analogs: CBD, 7-COOH-CBD, Abnormal CBD, CBDA-A and olivetolic acid.
MeSH term(s)	Cannabinoids/metabolism ; Cannabidiol ; Cannabis ; Immunoassay ; Carboxylic Acids
Chemical Substances	Cannabinoids ; Cannabidiol (19GBJ60SN5) ; olivetol (65OP0NEZ1P) ; Carboxylic Acids
Language	English
Publishing date	2023-08-21
Publishing country	England
Document type	Journal Article
ZDB-ID	752391-9
ISSN	1945-2403 ; 0146-4760
ISSN (online)	1945-2403
ISSN	0146-4760
DOI	10.1093/jat/bkad059
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Article ; Online: Effects of simulation-based flipped classroom in developing head and neck examination skills in dental students.

Fischer, Kathleen M / Sekula, Michael N / Hannigan, Joseph D / Vaught, Randall L / House, Holly / De Souza, Grace M / Williams, Tarin T

Journal of dental education

2024

Abstract: Objectives: To evaluate the effectiveness of a simulation-based flipped classroom in developing dental students' head and neck examination skills.: Methods: Second-year dental students (n = 118) participated in a simulation-based flipped classroom ... ...

Abstract	Objectives: To evaluate the effectiveness of a simulation-based flipped classroom in developing dental students' head and neck examination skills. Methods: Second-year dental students (n = 118) participated in a simulation-based flipped classroom experience. A pre-class recorded lecture and video were posted online one week before the simulation date. In class, students completed a pre-quiz assessing pre-class coursework understanding of head and neck examination content. Then, students attended a question-and-answer session before the patient simulation. A formative assessment of head and neck examination simulation on a patient in the clinic was completed. Lastly, students completed an in-class post-quiz assessing understanding of head and neck examination content after the simulation, classroom simulation discussion, and open-response survey. Results: Student post-quiz scores were significantly higher than pre-quiz scores, with an average improvement of 4.8 ± 7.2 percentage points. There was no difference between male and female improvement in scores. Student survey responses indicated that students liked combining simulation and flipped classroom methodology, flexibility with their schedules, learning at their pace, and opportunities for a deeper level of learning. Students reported wanting more practice sessions for their technical skills and more accessibility to faculty. Conclusions: According to this study's results, students had significantly higher post-quiz scores than pre-quiz scores and reported positive perceptions of this combined teaching technique. A simulation-based flipped classroom might be an effective teaching approach for developing head and neck examination skills that can be applied at other dental facilities with potentially similar results.
Language	English
Publishing date	2024-02-13
Publishing country	United States
Document type	Journal Article
ZDB-ID	410579-5
ISSN	1930-7837 ; 0022-0337
ISSN (online)	1930-7837
ISSN	0022-0337
DOI	10.1002/jdd.13490
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Zs.A 428: Show issues

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Article ; Online: Determination of 24,25-dihydroxyvitamin D

Wise, Stephen A / Hahm, Grace / Burdette, Carolyn Q / Tai, Susan S-C / Camara, Johanna E / Sempos, Christopher T / Williams, Emma L

The Journal of steroid biochemistry and molecular biology

2023 Volume 231, Page(s) 106318

Abstract: Ninety archived human serum samples from the Vitamin D External Quality Assessment Scheme (DEQAS) were analyzed using a reference measurement procedure (RMP) based on isotope dilution liquid chromatography - tandem mass spectrometry (ID LC-MS/MS) for the ...

Abstract	Ninety archived human serum samples from the Vitamin D External Quality Assessment Scheme (DEQAS) were analyzed using a reference measurement procedure (RMP) based on isotope dilution liquid chromatography - tandem mass spectrometry (ID LC-MS/MS) for the determination of 24,25-dihydroxyvitamin D
MeSH term(s)	Humans ; Chromatography, Liquid ; Tandem Mass Spectrometry/methods ; Vitamin D ; Vitamins ; Calcifediol ; 24,25-Dihydroxyvitamin D 3
Chemical Substances	24,25-dihydroxyvitamin D ; Vitamin D (1406-16-2) ; Vitamins ; Calcifediol (P6YZ13C99Q) ; 24,25-Dihydroxyvitamin D 3 (40013-87-4)
Language	English
Publishing date	2023-05-09
Publishing country	England
Document type	Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID	1049188-0
ISSN	1879-1220 ; 0960-0760
ISSN (online)	1879-1220
ISSN	0960-0760
DOI	10.1016/j.jsbmb.2023.106318
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Article ; Online: A randomized-controlled pilot trial of telemedicine-delivered cognitive-behavioral therapy tailored for interstitial cystitis/bladder pain syndrome.

McKernan, Lindsey C / McGonigle, Trey / Vandekar, Simon N / Crofford, Leslie J / Williams, David A / Clauw, Daniel J / Bruehl, Stephen / Corbett, Blythe A / Dmochowski, Roger R / Walsh, Elizabeth G / Kelly, Anna Grace / Sutherland, Susanna L / Connors, Erin L / Ryden, Anna / Reynolds, William Stuart

Pain

2024

Language	English
Publishing date	2024-02-27
Publishing country	United States
Document type	Journal Article
ZDB-ID	193153-2
ISSN	1872-6623 ; 0304-3959
ISSN (online)	1872-6623
ISSN	0304-3959
DOI	10.1097/j.pain.0000000000003188
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Article: Increased levels of anti-BSA antibodies in children with Down syndrome.

Grace, Sian L / Mortimer, Georgina L / Kozhakhmetova, Aizhan / Leveret, Jamie / Newton, Richard / Reimand, Koit / Shield, Julian P H / Uibo, Raivo / Williams, Alistair J K / Gillespie, Kathleen M

Frontiers in endocrinology

2023 Volume 14, Page(s) 1056925

Abstract: Introduction: Autoimmune diabetes occurs more often in the first 2 years of life in children with Down syndrome (DS) compared with the general population. We previously observed increased frequencies of islet autoantibodies, including insulin ... ...

Abstract	Introduction: Autoimmune diabetes occurs more often in the first 2 years of life in children with Down syndrome (DS) compared with the general population. We previously observed increased frequencies of islet autoantibodies, including insulin autoantibodies (IAA), in children with DS. Assays for IAA using Methods: Samples were available from two populations with DS: one from the UK, (UK DS cohort n=106, 58 male, median age 12.5 years) and one from Estonia (Estonian DS cohort: n=121, 65 male, median age 9.75 years). A UK control population was provided by sex and age-matched healthy siblings of probands participating in the Bart's Oxford (BOX) family study of type 1 diabetes. A competitive-displacement radiobinding assay (RBA) and a Dissociation Enhanced Lanthanide Fluoroimmunoassay (DELFIA) were developed to measure and confirm anti-BSA antibody levels. HLA class II genotype was analysed by PCR using sequence specific primers (PCR-SSP). Results: Overall, levels of anti-BSA antibodies were increased in those with DS compared with controls (p<0.0001) but this was not HLA associated. Conclusion: Increased levels of anti-BSA antibodies may reflect a defect in immune maturation or increased gut permeability in children with DS, increasing their risk of developing autoimmunity.
MeSH term(s)	Animals ; Female ; Cattle ; Child ; Humans ; Male ; Serum Albumin, Bovine ; Down Syndrome ; Diabetes Mellitus, Type 1/genetics ; Autoantibodies ; Insulin
Chemical Substances	Iodine-125 (GVO776611R) ; Serum Albumin, Bovine (27432CM55Q) ; Autoantibodies ; Insulin
Language	English
Publishing date	2023-02-03
Publishing country	Switzerland
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2592084-4
ISSN	1664-2392
ISSN	1664-2392
DOI	10.3389/fendo.2023.1056925
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Article ; Online: MetSim: Integrated Programmatic Access and Pathway Management for Xenobiotic Metabolism Simulators.

Groff, Louis / Williams, Antony / Shah, Imran / Patlewicz, Grace

Chemical research in toxicology

2024

Abstract: Xenobiotic metabolism is a key consideration in evaluating the hazards and risks posed by environmental chemicals. A number of software tools exist that are capable of simulating metabolites, but each reports its predictions in a different format and ... ...

Abstract	Xenobiotic metabolism is a key consideration in evaluating the hazards and risks posed by environmental chemicals. A number of software tools exist that are capable of simulating metabolites, but each reports its predictions in a different format and with varying levels of detail. This makes comparing the performance and coverage of the tools a practical challenge. To address this shortcoming, we developed a metabolic simulation framework called MetSim, which comprises three main components. A graph-based schema was developed to allow metabolism information to be harmonized. The schema was implemented in MongoDB to store and retrieve metabolic graphs for subsequent analysis. MetSim currently includes an application programming interface for four metabolic simulators: BioTransformer, the OECD Toolbox, EPA's chemical transformation simulator (CTS), and tissue metabolism simulator (TIMES). Lastly, MetSim provides functions to help evaluate simulator performance for specific data sets. In this study, a set of 112 drugs with 432 reported metabolites were compiled, and predictions were made using the 4 simulators. Fifty-nine of the 112 drugs were taken from the Small Molecule Pathway Database, with the remainder sourced from the literature. The human models within BioTransformer and CTS (Phase I only) and the rat models within TIMES and the OECD Toolbox (Phase I only) were used to make predictions for the chemicals in the data set. The recall and precision (recall, precision) ranked in order of highest recall for each individual tool were CTS (0.54, 0.017), BioTransformer (0.50, 0.008), Toolbox
Language	English
Publishing date	2024-04-10
Publishing country	United States
Document type	Journal Article
ZDB-ID	639353-6
ISSN	1520-5010 ; 0893-228X
ISSN (online)	1520-5010
ISSN	0893-228X
DOI	10.1021/acs.chemrestox.3c00398
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Article: Evaluation of Strontium Interference in Calcium Measurement Procedures and Content in Supplements as Measured by ICP-MS.

Williams, Grace R / Downs, John W / Wolf, Carl E / Cumpston, Kirk L / Tobarran, Natasha / Wills, Brandon K / Bachmann, Lorin M

The journal of applied laboratory medicine

2023 Volume 8, Issue 2, Page(s) 307–318

Abstract: ... of 1.0 mg/dL (0.114 mmol/L), 2.5 mg/dL (0.284 mmol/L), and 5.0 mg/Dl (0.568 mmol/L) resulted in mean ... mg/dL (0.568 mmol/L). An in-house-developed ICP-MS assay for strontium in commercially available ... mmol/L). Strontium recovery for the ICP-MS assay was 97.1% to 105.3%. The largest amount of strontium ...

Abstract	Background: Bone health supplements containing strontium are available without prescription, however, the effects of strontium interference on clinical laboratory calcium measurement procedures are unknown. Methods: To evaluate strontium interference on total calcium measurements, plasma pools with exogenously added strontium were measured by 3 total calcium measurement procedures. For ionized calcium measurements, whole blood pools prepared with exogenously added strontium were measured by 2 ionized calcium measurement procedures. An inductively coupled plasma mass spectrometry assay (ICP-MS) was validated for research measurements of strontium content in commercially available supplements. Results: Exogenous strontium addition to plasma caused positive bias for total calcium measurements. Strontium concentrations of 1.0 mg/dL (0.114 mmol/L), 2.5 mg/dL (0.284 mmol/L), and 5.0 mg/Dl (0.568 mmol/L) resulted in mean biases of 1.9% to 3.5%, 4.9% to 9.0%, and 10.8% to 19.2%, respectively, for total calcium measurement procedures. Biases for ionized calcium measurements were less than 4.5% for a strontium concentration of 5.0 mg/dL (0.568 mmol/L). An in-house-developed ICP-MS assay for strontium in commercially available supplements exhibited within-laboratory and within-run coefficients of variation of less than 3%, and a linear response was obtained over the assay analytical measurement range of 10 to 100 000 ng/mL (0.0001 to 1.141 mmol/L). Strontium recovery for the ICP-MS assay was 97.1% to 105.3%. The largest amount of strontium measured in dietary supplements was 395 mg in a 1054 mg tablet. Conclusions: Some dietary supplements contain larger amounts of strontium than indicated on the product label. High concentrations of strontium may cause significant interference for total calcium measurement procedures, but ionized calcium measurement procedures are not significantly affected.
MeSH term(s)	Humans ; Calcium ; Dietary Supplements ; Biological Assay ; Correlation of Data ; Strontium
Chemical Substances	Calcium (SY7Q814VUP) ; Strontium (YZS2RPE8LE)
Language	English
Publishing date	2023-01-26
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
ISSN	2576-9456
ISSN	2576-9456
DOI	10.1093/jalm/jfac092
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Article ; Online: Immunomodulators and risk for breakthrough COVID-19 after third SARS-CoV-2 mRNA vaccine among patients with rheumatoid arthritis: a cohort study.

Schiff, Abigail E / Wang, Xiaosong / Patel, Naomi J / Kawano, Yumeko / Hanberg, Jennifer L / Kowalski, Emily N / Cook, Claire E / Vanni, Kathleen Mm / Qian, Grace / Bade, Katarina J / Saavedra, Alene A / Srivatsan, Shruthi / Williams, Zachary K / Venkat, Rathnam K / Wallace, Zachary S / Sparks, Jeffrey A

Annals of the rheumatic diseases

2024 Volume 83, Issue 5, Page(s) 680–682

MeSH term(s)	Humans ; SARS-CoV-2 ; COVID-19 Vaccines ; Cohort Studies ; mRNA Vaccines ; COVID-19/prevention & control ; Immunologic Factors ; Arthritis, Rheumatoid ; Vaccination ; Antibodies, Viral
Chemical Substances	COVID-19 Vaccines ; mRNA Vaccines ; Immunologic Factors ; Antibodies, Viral
Language	English
Publishing date	2024-04-11
Publishing country	England
Document type	Letter
ZDB-ID	7090-7
ISSN	1468-2060 ; 0003-4967
ISSN (online)	1468-2060
ISSN	0003-4967
DOI	10.1136/ard-2023-225162
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