3 research outputs found
MOESM1 of Sarcopenic obesity assessed using dual energy X-ray absorptiometry (DXA) can predict cardiovascular disease in patients with type 2 diabetes: a retrospective observational study
Additional file 1. Clinical characteristics and medications at baseline in the four categories of body composition (normal, sarcopenia, obesity, and sarcopenic obesity) classified using android fat mass, percent of body fat and body mass index. The baseline characteristics and medications in the four categories of body composition classified according to each indicator of obesity other than A/G ratio are shown in Tables S1–S6. Tables S1, S3, S5. The baseline characteristics when using android fat mass, percent of body fat, and body mass index for the classification of obesity, respectively. Tables S2, S4, S6. The medication when using android fat mass, percent of body fat, and body mass index for the classification of obesity, respectively
Ipragliflozin Reduces Epicardial Fat Accumulation in Non-Obese Type 2 Diabetic Patients with Visceral Obesity: A Pilot Study
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Biochemical Gas Sensors (Biosniffers) Using Forward and Reverse Reactions of Secondary Alcohol Dehydrogenase for Breath Isopropanol and Acetone as Potential Volatile Biomarkers of Diabetes Mellitus
This study describes two biosniffers
to determine breath acetone
and isopropanol (IPA) levels and applies them for breath measurement
in healthy subjects and diabetic patients. Secondary alcohol dehydrogenase
(S-ADH) can reduce acetone and oxidize nicotinamide adenine dinucleotide
(NADH to NAD<sup>+</sup>) in a weak acid environment. NADH can be
excited by 340 nm excitation lights and subsequently emit 490 nm fluorescence.
Therefore, acetone can be measured by the decrease in NADH fluorescence
intensity. S-ADH can also oxidize IPA and reduce NAD<sup>+</sup> to
NADH when it is in an alkaline environment. Thus, IPA can be detected
by the increase of fluorescence. The developed biosniffers show rapid
response, high sensitivity and high selectivity. The breath acetone
and IPA analysis in healthy subjects shows that the mean values were
750.0 ± 434.4 ppb and 15.4 ± 11.3 ppb. Both acetone and
IPA did not show a statistical difference among different genders
and ages. The breath acetone analysis for diabetic patients shows
a mean value of 1207.7 ± 689.5 ppb, which was higher than that
of healthy subjects (<i>p</i> < 1 × 10<sup>–6</sup>). In particularly, type-1 diabetic (T1D) patients exhaled a much
higher concentration of acetone than type-2 diabetic (T2D) patients
(<i>p</i> < 0.01). The breath IPA also had a higher concentration
in diabetic patients (23.1 ± 20.1 ppb, <i>p</i> <
0.01), but only T2D patients presented a statistical difference (23.9
± 21.3 ppb, <i>p</i> < 0.01). These findings are
worthwhile in the study of breath biomarkers for diabetes mellitus
diagnosis. Additionally, the developed biosniffers provide a new technique
for volatolomics research