Body weight was recorded to the nearest 0.1 kg and was measured in the morning in the fasting state with patients wearing light clothing without shoes and using a flat scale (Tanita WB-110MA, Japan). Height was measured in a stadiometer (Seca Mode 220, Hamburg Germany) and recorded to the nearest 0.1 cm. Body mass index (BMI) was calculated as weight (kg) divided by height squared (m2). Then, participants were asked to sit for 5 min, after which three consecutive blood pressure measurements were recorded at an interval of 1–2 min. Systolic and diastolic blood pressures were recorded by trained personnel at baseline using an OMRON HEM-907XL (OMRON, Kyoto, Japan) device.
Wb 110ma
Manufactured by Tanita
Sourced in Japan
The WB-110MA is a clinical-grade precision scale designed for laboratory use. It features a large weighing platform, high accuracy measurements, and easy-to-read digital display. The scale is capable of weighing subjects up to 220 kg with a readability of 0.1 kg.
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Lab products found in correlation
9 protocols using wb 110ma
1
Anthropometric and Blood Pressure Measurements
2
Longitudinal Hormone and BMI Evaluation
3
Anthropometric Measurements Protocol
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All anthropometric measurements were recorded after a ≥12-h fast. Body weight was measured with light clothing and without shoes using a flat scale (Tanita WB-110MA, Tokyo, Japan) and was recorded to the nearest 0.1 kg. Height was measured on a stadiometer (Seca Model 220, Hamburg, Germany) and was recorded to the nearest 0.1 cm. BMI was calculated as weight (in kg) divided by height2 (in m2). The waist and hip circumferences were measured using a stretch-resistant tape.
4
Comprehensive Assessment of Body Composition
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Height was measured to the nearest millimeter (235 Heightronic Digital Stadiometer; QuickMedical, Issaquah, WA, USA), and the children were then weighed to the nearest 0.1 kg (Tanita WB-110 MA; Tanita, Amsterdam, The Netherlands) while barefoot and wearing light clothing. Whole-body and leg-bone mineral density (BMD) and bone mineral content (BMC), as well as lean body mass and fat mass index (FMI), were estimated with a whole-body dual-energy X-ray absorptiometry (Lunar Prodigy; GE Medical Systems, Madison, WI, USA) using Encore software version 13.5 (Encore, Madison, WI, USA), with a coefficient of variation for whole-body variables of <1%. The children were instructed to fast for at least 2 hours and to visit the toilet before the scan. The children were scanned in a supine position wearing light clothing (24 (link)).
5
Anthropometric Characterization of Study Population
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An overview of the population included in the study can be found in Table 1 . Height was measured to the nearest millimetre (235 Heightronic Digital Stadiometer, QuickMedical, Issaquah, WA, US) and the children were then weighed to the nearest 0.1 kg (Tanita WB-110MA, Tanita, Europe) while barefoot and wearing light clothing. Finally, whole-body composition was determined by Dual-energy X-ray absorptiometry (Lunar Prodigy; GE Medical Systems, Madison, Wisconsin, USA) using Encore software version 13.5 (Encore, Madison, USA). These measures were obtained to characterize the population included in the study.
6
Anthropometric Measurements in Vegans
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Vegan participants were weighed on an electronic scale (TANITA WB-110MA, Tanita Corporation of America, Arlington Heights, Illinois, USA) without shoes, dressed in light clothing or underwear after having emptied their bladder. The height of the participants was measured to the nearest 0.5 cm without shoes, using a wall-mounted stadiometer (ADE MZ10023, ADE, Hamburg, Germany). Anthropometric measures of the DANSDA population were self-reported as previously described [2 ].
7
Anthropometric Measurements Protocol
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Height was only measured at the baseline. The participant was asked to remove shoes and to stand upright with the back to the wall-mounted stadiometer so that the back of the head, back, and buttock touched the stadiometer. The participant was further instructed to look straight ahead and to hold the arms relaxed, hanging next to the body. The height was recorded in centimeters to the nearest 0.5 cm.
Body weight and waist circumference were measured after the participant had emptied the bladder. Body weight was measured using a calibrated digital scale (Tanita WB-110MA). The participant was weighed in light clothes and asked to stand in the middle of the platform on the scale with a straight neck and eyes looking straight ahead while distributing the weight evenly on both feet. Body weight was recorded in kilograms to the nearest 0.1 kg.
The waist circumference was measured with the participant standing to ensure equal weight distribution on both feet. The waist circumference was measured twice on the skin with a non-elastic band to the nearest 0.5 cm between the lower rib and the hip crest, and when the participant exhaled. The average of these two measurements was used.
Body weight and waist circumference were measured after the participant had emptied the bladder. Body weight was measured using a calibrated digital scale (Tanita WB-110MA). The participant was weighed in light clothes and asked to stand in the middle of the platform on the scale with a straight neck and eyes looking straight ahead while distributing the weight evenly on both feet. Body weight was recorded in kilograms to the nearest 0.1 kg.
The waist circumference was measured with the participant standing to ensure equal weight distribution on both feet. The waist circumference was measured twice on the skin with a non-elastic band to the nearest 0.5 cm between the lower rib and the hip crest, and when the participant exhaled. The average of these two measurements was used.
8
DXA Scanning for Body Composition in Children
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The children were weighed barefooted and wearing light clothing (Tanita WB-110MA, Tanita, Europe) and their height was measured (235 Heightronic Digital Stadiometer, QuickMedical, Issaquah, WA, US). A whole-body (wb) DXA scan (Lunar Prodigy; E Medical Systems, Madison, Wisconsin, USA) using Encore software version 13.5 (Encore, Madison, USA) was performed in accordance to standard procedures to estimate whole-body and leg aBMD and BMC as well as lean body mass. The children were scanned in a supine position. The manufacturer states a coefficient of variation (CV) for whole-body bone variables less than 1%. This is supported by a study that evaluated the leg region in children from a whole-body scan and reported CV values of 1.11 to 1.36% for regional bone parameters [28 (link)]. For each child, pretesting and posttesting were conducted at the same time of day (within one hour) and the children were instructed to fast for at least 2 hr and to visit the toilet before the scan.
9
Comprehensive Metabolic Profiling in Fasting Participants
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All clinical parameters were measured after overnight fasting by the study personnel. Height was measured at study inclusion. Weight was measured wearing light clothes and to the nearest 0.1 kg (WB-110MA, Tanita, Tokyo, Japan), and a BMI (kg/m2) was calculated (weight (kg)/height (m)2). Total body-fat percentage was measured using the same Dual-energy X-ray Absorptiometry (DXA) scanner throughout the study (Discovery A, Hologic, Bedford, USA). Peak oxygen uptake (VO2 peak) rates were assessed with a max cycle ergometer test.
Plasma C-reactive protein (CRP) was measured with a turbidimetric immunoassay, plasma cholesterol, low-density lipoprotein (LDL), high-density lipoprotein (HDL), very low-density lipoprotein (VLDL) and triglycerides with the enzymatic colourimetric method (COBAS 6000/8000, Roche, Basel, Switzerland). Glycated haemoglobin A1c (HbA1C) was measured with high-performance liquid chromatography (HLC 723 G8, TOSOH, Tokyo, Japan). Haemoglobin was measured with a photometric cyanide-free SLS method (XN 1000/9000, SYSMEX, Kobe, Japan). All measurements were analysed on the same day as the test visits at the Department of Clinical Biochemistry, Hvidovre Hospital, Hvidovre, Denmark.
Plasma C-reactive protein (CRP) was measured with a turbidimetric immunoassay, plasma cholesterol, low-density lipoprotein (LDL), high-density lipoprotein (HDL), very low-density lipoprotein (VLDL) and triglycerides with the enzymatic colourimetric method (COBAS 6000/8000, Roche, Basel, Switzerland). Glycated haemoglobin A1c (HbA1C) was measured with high-performance liquid chromatography (HLC 723 G8, TOSOH, Tokyo, Japan). Haemoglobin was measured with a photometric cyanide-free SLS method (XN 1000/9000, SYSMEX, Kobe, Japan). All measurements were analysed on the same day as the test visits at the Department of Clinical Biochemistry, Hvidovre Hospital, Hvidovre, Denmark.
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