3 research outputs found
Supplementary Material for: Single Nucleotide Polymorphisms in Adiponectin Gene Are Not Directly Associated with Increased Risk of Obstructive Sleep Apnea Syndrome in a Chinese Han Population
<i>Purpose:</i> This study aims to test the possible correlation between single nucleotide polymorphisms (SNPs) in the adiponectin gene and increased risk of obstructive sleep apnea syndrome (OSAS) in a Chinese Han population. <i>Materials and Methods:</i> A total of 266 subjects were enrolled into the study to detect 9 SNPs in the adiponectin gene. Multivariate unconditional logistic regression analysis, adjusted for gender and age, was used to estimate the associations of these SNPs with OSAS risk. <i>Results:</i> No evidence of a direct association was observed between these SNPs and the risk of OSAS in the Chinese Han population. However, the stratified analysis also revealed a remarkable genotype difference for SNP rs6773957 between cases and controls in the overweight subgroup (<i>p </i>< 0.05). In addition, the allele or genotype distributions of rs12495941, rs182052, and rs16861205 had significant differences with regard to the severity of OSAS (<i>p </i>< 0.05). No differences were identified in the other subgroups. <i>Conclusion:</i> The current research demonstrated that the SNPs in the adiponectin gene did not represent susceptibility loci for OSAS in Chinese Han individuals overall. However, variants of rs6773957 have an association with OSAS in overweight individuals. In addition, polymorphisms of rs12495941, rs182052, and rs16861205 are associated with the severity of OSAS
PowerPoint Slides for: Prognostic Value of the Delivery Dialysis Dose on Twice-Weekly Hemodialysis Patients
<p><b><i>Background:</i></b> Few studies have evaluated the prognostic
value of dialysis dose in twice-weekly hemodialysis (HD). A single-pool
Kt/V (spKt/V) over 1.70 may benefit patients receiving twice-weekly
maintenance HD. <b><i>Methods:</i></b> This is a multicenter randomized
controlled trial performed on 163 patients from 17 dialysis centers in
Shanghai who were allocated to high- (<i>n</i> = 98) and standard-dose groups (<i>n</i>
= 65) and followed through 96 weeks of study period. Therapeutic
approaches were given to increase spKt/V to over 1.70 in the high-dose
group. Data were collected every 12-24 weeks. The primary outcomes were
all-cause mortality and major adverse cardio-cerebrovascular events
(MACEs) occurrence, and secondary outcomes included residual kidney
function (RKF) and health-related quality of life (HR-QOL). <b><i>Results:</i></b> The spKt/V in high-dose and standard-dose groups were 1.80 ± 0.23 and 1.55 ± 0.19, respectively, after an 8-week intervention (<i>p</i>
< 0.001). At the end of the study, SF-36 physical function and total
score in high-dose group were 82 (69-90) and 74 (47-84), respectively,
both of which were higher than those in the standard-dose group. Decline
in urine volume was observed in both groups with no significant
difference (<i>p</i> = 0.431). No difference was found in overall survival between the 2 groups (<i>p</i> = 0.580). The 1-year MACE-free survival for high-dose group was 84.49%, better than 76.72% for standard-dose group (<i>p</i> = 0.029). <b><i>Conclusions:</i></b>
Higher spKt/V is also associated with MACE-free survival and better
HR-QOL, especially in physical function aspect for twice-weekly dialysis
patients. Increasing spKt/V over 1.70 in twice-weekly HD population
does not cause loss of RKF.</p
Supplementary Material for: Prognostic Value of the Delivery Dialysis Dose on Twice-Weekly Hemodialysis Patients
<p><b><i>Background:</i></b> Few studies have evaluated the prognostic
value of dialysis dose in twice-weekly hemodialysis (HD). A single-pool
Kt/V (spKt/V) over 1.70 may benefit patients receiving twice-weekly
maintenance HD. <b><i>Methods:</i></b> This is a multicenter randomized
controlled trial performed on 163 patients from 17 dialysis centers in
Shanghai who were allocated to high- (<i>n</i> = 98) and standard-dose groups (<i>n</i>
= 65) and followed through 96 weeks of study period. Therapeutic
approaches were given to increase spKt/V to over 1.70 in the high-dose
group. Data were collected every 12-24 weeks. The primary outcomes were
all-cause mortality and major adverse cardio-cerebrovascular events
(MACEs) occurrence, and secondary outcomes included residual kidney
function (RKF) and health-related quality of life (HR-QOL). <b><i>Results:</i></b> The spKt/V in high-dose and standard-dose groups were 1.80 ± 0.23 and 1.55 ± 0.19, respectively, after an 8-week intervention (<i>p</i>
< 0.001). At the end of the study, SF-36 physical function and total
score in high-dose group were 82 (69-90) and 74 (47-84), respectively,
both of which were higher than those in the standard-dose group. Decline
in urine volume was observed in both groups with no significant
difference (<i>p</i> = 0.431). No difference was found in overall survival between the 2 groups (<i>p</i> = 0.580). The 1-year MACE-free survival for high-dose group was 84.49%, better than 76.72% for standard-dose group (<i>p</i> = 0.029). <b><i>Conclusions:</i></b>
Higher spKt/V is also associated with MACE-free survival and better
HR-QOL, especially in physical function aspect for twice-weekly dialysis
patients. Increasing spKt/V over 1.70 in twice-weekly HD population
does not cause loss of RKF.</p