The postnatal development of immunoreactive TRH in the central nervous system (CNS), serum TSH and thyroid hormones was studied in both male and female normal rats. While in most structures of the CNS, TRH increased until day 20\p=n-\30,serum TSH values peaked at day 15 as did T4. Significant differences were also obtained between both sexes in these parameters. These data further support the fact that pituitary-thyroid axis maturation is independent of brain TRH.

Background and Aims Torque teno virus (TTV) is a non-pathogenic anellovirus whose replication kinetics reflects the overall state of immunosuppression. Although chronic kidney disease (CKD) induces a well-stabilised dysfunction of the immune system, long-term use of renal replacement therapies (RRT) itself could also modify the immune response. Method We analyzed TTV DNA loads at baseline (in the pre-transplant assessment), day 7 and months 1, 3,6 and 12 after kidney transplantation (KT). Recipients were categorized according to their RRT status: pre-emptive KT (pre-KT), hemodialysis (HD) and peritoneal dialysis (PD). TTV DNA load was measured by real-time polymerase chain reaction. Results A total of 221 CKD patients were analyzed. The mean age was 53.9 ± 15.7 years, 72.4% were males, and hypertension (85.1%) and diabetes (30.1%) were the most common comorbidities. According to the pre-transplant TTR status, 159 (72.0%) were on HD, 35 (15.8%) on PD and 27 (12.2%) received pre-KT. There were no differences in baseline comorbidities or age between patients according to their RRT status, except for residual diuresis (P <0.01). HD patients had higher serum albumin levels than patients receiving pre-KT or PD (4.4 ± 0.5 vs. 4.1 ± 0.6 vs. 3.9 ± 0.4 g/dL, respectively, P <0.01). PD patients exhibited higher TTV DNA load (3.4 ±1.2 log10 copies/mL) than HD (2.8 ± 1.6 log10 copies/mL) or pre-KT patients (2.4 ± 2.1 log10 copies/mL), although the differences were not statistically significant. PD patients had lower time on dialysis than HD patients (18.4± 16.2 vs. 37.5± 53.6 months, respectively; P = 0.038). Although PD patients had higher TTV DNA load during the post-transplant follow-up than HD and pre-KT patients, viral kinetics were comparable across these three groups by month 12 after transplantation. Time on dialysis was not associated with TTV DNA load (P = 0.18). RRT status was not associated with the incidence of post-transplant infection or a composite of opportunistic infection and/or de novo malignancy. Conclusion TTV DNA load could be useful identifying KT recipients at high risk of immunosuppression-related complications. Although PD patients presented a non-significant higher TTV DNA load, we did not find differences according to the modality of prior RRT or the time on dialysis.

No abstract

Background and Aims Peritoneal dialysis (PD) fluids used colloid or crystalloid solutions to achieve ultrafiltration. Here we presented our clinical experience with the intraperitoneal (IP) use of mixed solutions (MS) (crystalloid plus colloid) to treat overhydration. Method We studied the kinetics of 4-hour single-dwell exchange using 2L MS in 3 different sessions. We analysed IP fluids and IP pressure at 0,30,60,120 and 240 min plus blood samples at 0, 120 and 240 min. MS kinetics were compared with standard 4-hour 3.86 % glucose (GS) exchange. MS composition. We modified a single-dwell exchange of 2L Icodextrin (Extraneal, Baxter®) by adding a continuous 50% glucose infusion (50g Glucose per 100mL) in an aseptic technique through infusion pump (42 ml/h) over 4 hours. Results MS exchange induced a progressive increase in IP pressure with an inverse decrease in IP sodium, without significant changes in IP glucose or osmolarity. MS exchanges were well tolerated without side effects (total 25 sessions). We did not observe any remarkable change in bloods samples during the MS exchange. The combination fluid enhanced net ultrafiltration (mean 1030 ml) compared with GS (650 ml). Although the net glucose dispensed was slightly higher with MS (79 g MS vs 77.2 g GS), similar net glucose absorption was observed (49.8 g MS vs 49.9g GS) and smaller maximum intraperitoneal glucose levels (1739 mg/dL at 120 min with MS vs 2695 mg/dL with GS at 0 min). GS induced a faster initial reduction in dialysate sodium concentration while MS maintained the sodium sieving over 4-hour dwell enhancing net ultrafiltration due to sustained IP glucose concentration. Conclusion The combination fluid could be a new strategy to enhance ultrafiltration in PD patients, leaded by colloid osmosis at the beginning of PD exchange maintained by crystalloid osmosis. Figure (A) Intraperitoneal kinetics of MIXED SOLUTION for IP sodium (Na+ PF), Osmolarity PF and intraperitoneal pressure. (B, C, D) Comparison between MIXED SOLUTIONS (black line) vs Glucose solution 3,86 % (gray line) intraperitoneal kinetcs for sodium (B), intraperitoneal pressure (C) and glucose (D).

No abstract