The Effects of Hydration Status on Heart Rate Variability Following Supramaximal Intensity Exercise

Heart rate variability (HRV) is a non-invasive method used to monitor physiological stress via assessment of sympathetic and parasympathetic regulations and can indicate an individual’s recovery and readiness to exercise. Evidence suggests dehydration negatively impacts HRV; however, the influence of hydration status on HRV following supramaximal resistance exercise (RE) is unknown. PURPOSE: To investigate the effect of hydration status on HRV indices following supramaximal intensity RE. METHODS: 14 recreationally resistance-trained men (age, 21 ± 2 years; height, 176.25 ± 5.84 cm; weight, 81.31 ± 12.77 kg) participated in this study. In a randomized, counterbalanced order, participants performed a supramaximal intensity RE protocol in a euhydrated (EUH; urine specific gravity [USG] \u3c 1.020) and a dehydrated (DEH; USG \u3e 1.020) state, with conditions separated by 2 weeks. HRV indices (standard deviation of normal sinus beats [SDNN], root mean square of successive differences between normal heartbeats [RMSSD], high frequency power [HF], low frequency power [LF], LF:HF ratio, standard deviation of Poincaré plot perpendicular to [SD1] and along the line of identity [SD2]) were measured with participants lying in a supine position for 5 minutes in a dark room at baseline, immediately post-, 1hr-, 2hr-, and 3hr post-RE. Repeated measure analysis of variance was used to determine the effect of hydration status on HRV indices at each timepoint, with Bonferroni corrections for post-hoc analysis. RESULTS: RMSSD was significantly higher 1hr post-exercise in EUH (30.69 ± 7.09 ms) compared to DEH (16.31 ± 2.44 ms; p = 0.04). Similarly, HF power was significantly higher 1hr post-exercise in EUH (32.49 ± 4.12 %) compared to DEH (16.63 ± 2.71 %; p \u3c 0.01). In contrast, LF power was lower 1hr post-exercise in EUH (57.74 ± 3.62 %) compared to DEH (75.95 ± 3.42 %; p = 0.02), with LF:HF ratio significantly lower in EUH (2.36 ± 0.62) than DEH (6.21 ± 1.34; p = 0.01). SD1 was significantly greater 1hr post-exercise in EUH (21.74 ± 5.03 ms) than DEH (11.54 ± 1.73 ms; p = 0.04). No significant condition by time effects were observed for SDNN and SD2, or at remaining timepoints. CONCLUSION: These findings indicate that recovery and readiness to exercise are impaired 1hr following supramaximal intensity RE in a dehydrated state. However, impairments were ameliorated 2-3hrs proceeding the RE bout

Early detection of Toxoplasma infection by molecular monitoring of Toxoplasma gondii in peripheral blood samples after allogeneic stem cell transplantation

International audienceBackground. Isolated case reports have shown that recipients of allogeneic hematopoietic stem cell transplants ( HSCTs) who develop toxoplasmosis may have circulating Toxoplasma gondii DNA in peripheral blood before the onset of clinical symptoms. Methods. We prospectively studied 106 T. gondii - seropositive adult recipients of HSCTs for the incidence of reactivation of toxoplasmosis in the first 6 months after transplantation. Toxoplasmosis infection ( TI) was defined by a positive result of polymerase chain reaction ( PCR) of peripheral blood specimens, whereas toxoplasmosis disease ( TD) was defined as an invasive infection. Results. The incidence of TI was 16% ( 95% confidence interval [ CI], 8% - 21%), whereas the incidence of TD was 16% ( 95% CI, 1% - 10%). In the 16 patients with TI, the incidence of disease was 38%, whereas it was 0% in patients without TI (P < .001). In most patients, the onset of TD or treatment for TI was preceded by an increase in the parasite load in peripheral blood samples, as determined by quantitative PCR. Conclusions. Toxoplasmosis occurs more commonly after HSCT than has previously been suggested, and routine PCR testing of peripheral blood specimens may be an appropriate tool for guiding preemptive therapy in patients at very high risk of developing invasive disease

25 Signatures

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Nuclear ribosomal internal transcribed spacer (ITS) region as a universal DNA barcode marker for Fungi

Six DNA regions were evaluated as potential DNA barcodes for Fungi, the second largest kingdom of eukaryotic life, by a multinational, multilaboratory consortium. The region of the mitochondrial cytochrome c oxidase subunit 1 used as the animal barcode was excluded as a potential marker, because it is difficult to amplify in fungi, often includes large introns, and can be insufficiently variable. Three subunits from the nuclear ribosomal RNA cistron were compared together with regions of three representative protein-coding genes (largest subunit of RNA polymerase II, second largest subunit of RNA polymerase II, and minichromosome maintenance protein). Although the protein-coding gene regions often had a higher percent of correct identification compared with ribosomal markers, low PCR amplification and sequencing success eliminated them as candidates for a universal fungal barcode. Among the regions of the ribosomal cistron, the internal transcribed spacer (ITS) region has the highest probability of successful identification for the broadest range of fungi, with the most clearly defined barcode gap between inter- and intraspecific variation. The nuclear ribosomal large subunit, a popular phylogenetic marker in certain groups, had superior species resolution in some taxonomic groups, such as the early diverging lineages and the ascomycete yeasts, but was otherwise slightly inferior to the ITS. The nuclear ribosomal small subunit has poor species-level resolution in fungi. ITS will be formally proposed for adoption as the primary fungal barcode marker to the Consortium for the Barcode of Life, with the possibility that supplementary barcodes may be developed for particular narrowly circumscribed taxonomic groups