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Precision xtra ketone monitoring system

Manufactured by Abbott
Sourced in United States

The Precision Xtra Ketone Monitoring System is a device designed for the measurement of ketone levels in the blood. It provides a convenient and accurate way to monitor ketone concentrations.

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5 protocols using precision xtra ketone monitoring system

1

Measuring Blood and Urine Ketones

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β-OHB ketone bodies were measured either in venous blood (hospital laboratory or bedside testing using the Precision Xtra Ketone Monitoring System (Abbott Laboratories, Lake Bluff, IL, USA)) and/or in urine using a dipstick. For those pediatric visits in which only urinary ketones levels were available, venous ketone levels were estimated using the formula and analysis presented in Supplementary Figure S1. Ketones levels in adults prior to commencing the diet were considered to be zero.
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2

Serum Biomarker Quantification in Mice

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Serum intact and total FGF23 levels were measured using commercially available mouse iFGF23 (recognizes intact FGF23 only) and cFGF23 (recognizes both intact and C‐terminal FGF23 peptides) ELISA assays (Immutopics, Carlsbad, CA, USA). Serum intact PTH was measured using the mouse PTH 1‐84 ELISA assay (Immutopics) and serum 1,25(OH)2D was measured by immunoassay (Immunodiagnostic Systems, Gaithersburg, MD, USA). Blood urea nitrogen (BUN), serum and urine calcium, phosphate, creatinine, and urinary albumin were measured using colorimetric assays (Pointe Scientific, Canton, MI, USA). Serum potassium was measured using turbidimetric assay (Stanbio, Boerne, TX, USA). Serum ketones were measured using the Precision Xtra ketone monitoring system (Abbott, Alameda, CA, USA). Urinary glucose was measured using Accu‐Chek Aviva glucometer (Roche, Indianapolis, IN, USA).
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3

Ketogenic Diet Effects on Muscle Mitochondria

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All animal procedures were approved (18-0101, 9 February 2018) by the institutional animal care and use committee at Brigham Young University. 5-month-old male Fisher 344 rats (n = 6/group) were acclimatized for 1 week after arrival at the animal facility and were then pair-fed with either standard diet (STD; Envigo Teklad Rodent Diet, 8604; 32% protein, 14% fat, 54% carbohydrate) or ketogenic diet (KETO; Envigo Teklad custom diet, TD.10911; 22.4% protein, 77.1% fat, 0.5% carbohydrate) for 4 weeks. Each day the chow remaining in the cage was weighed and replaced with fresh chow. Body weight for the rats was recorded weekly. At 4 weeks, the rats were euthanized and blood, gastrocnemius and quadriceps muscles were removed. Plasma ketone levels were measured using the Abbott Precision Xtra Ketone Monitoring System. White and red quadriceps muscle was separated and a small sample of the red quadriceps (~10 mg) was prepared for assessment of mitochondrial respiration as described above. The remaining muscle was frozen at the temperature of liquid nitrogen and stored at −90 °C for later analysis.
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4

Ionizing Radiation and Ketogenic Diet for Pancreatic Cancer

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Mia Paca-2 cells (pancreatic cancer cell line) were obtained from the American Type Culture Collection (ATCC). Mia Paca-2 cells were maintained in Dulbecco’s Modified Eagle’s Medium containing 10% FBS (Hyclone). Female 4 to 6 week old athymic nu/nu mice were purchased from Harlan Laboratories. Mice were housed in the Animal Care Facility at our institution and all procedures were approved by our Institutional Animal Care and Use Committee and conformed to NIH guidelines. Mice were subcutaneously injected with 2.5 × 106 Mia-Paca-2 pancreatic cancer cells into the right flanks. When tumors reached approximately 4 mm in diameter, mice were treated with ionizing radiation (12 Gy in 6 × 2 Gy fractions) or ionizing radiation combined with KD for 25 days as previously described (9 (link)). The 4:1 KetoCal® diet for the animal studies was purchased from Nutricia North America, Inc. (Gaithersburg, MD) and prepared as per the manufacturer’s instructions while the controls were fed standard mouse chow. Daily weighing of the unfinished food pellets monitored food intake. To ensure mice fed with KetoCal® were in ketosis, blood HbA1c was calculated using Crystal Chem mouse assay kit (Downers Grove, IL) and blood ketone levels were measured with the Precision Xtra ketone monitoring system (Abbott; Alameda, CA).
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5

Circadian Metabolite Profiling in Mice

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Tail vein blood samples were obtained from 6 months old WT and BACHD mice (n = 10 animals/genotype) kept for 3 months on a ND or KD at 6 time points during the sleep/wake cycle (ZT 2, 6, 10, 14, 18, 22). A small incision was made to access the tail vein to permit repeated withdrawals (under 3 μL per collection) with minimal pain and distress to the mice. At each specific ZT, mice were retrieved from the cages, placed on a stable surface and minimally restrained by the tail. Blood sampling was performed under normal room lighting (350 lux) for the testing times in the day, between ZT 0 and 12, and under dim red-light (3 lux) for those during the night (between ZT12 and 24). Blood flow was stopped by applying pressure with a sterile gauze to achieve hemostasis. Metabolite measurements were made in 1.5 μL blood samples using a commercially available ketone meter (Precision Xtra Ketone Monitoring System, Abbott Laboratories, Chicago, IL).
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