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effective interventions to reduce fall risk in persons with amputation will likely require strategies that adopt multi-objective approaches.

Since control of stepping is intrinsically multi-objective, developing effective interventions to reduce fall risk in persons with amputation will likely require strategies that adopt multi-objective approaches.

Although it is assumed that the presence of patellofemoral pain (PFP) may result in compensatory behaviors that can alter trunk kinematics and lower limb mechanics, the influence of the exacerbation of patellofemoral pain on trunk kinematics and lower limb mechanics during stair negotiation has not been established.

Does the exacerbation of PFP symptoms lead to altered trunk kinematics and lower limb mechanics during stair negotiation?

Three-dimensional kinematics and kinetics were obtained from 45 women with PFP during stair descent and ascent. Data were obtained before and after a pain exacerbation protocol. The variables of interest were peak trunk, hip, and knee flexion, and ankle dorsiflexion; peak hip, and knee extensor, and ankle plantarflexor moments. Paired t-tests were used to compare the variables of interest before and after pain exacerbation.

Following pain exacerbation, there was a decrease in peak knee extensor moment during stair descent (Effect size = -0.68; p = 0.01) and stair ascent do not seem to change their trunk, hip, and knee flexion or hip extensor moment during stair negotiation in response to symptom exacerbation.Our aim was to analyze characteristics of treatment failure with intravenous tigecycline monotherapy among adults with severe Clostridioides (Clostridium) difficile infection (CDI). A single-centre observational cohort study was performed between 2014 and 2018. Data were collected by charts review, diagnosis and severity were determined by ESCMID guidelines. Primary outcome was treatment failure, secondary outcomes were in-hospital mortality, relapse, colectomy, and complication rates. Independent predictors of failure were identified using logistic regression. Altogether 110 patients were included, failure occurred in 37.3%. Patients with failure frequently had chronic heart and pulmonary co-morbidities, peritonitis, higher CRP levels, ICU admittance rates and need for total parenteral nutrition and vasopressors. Mostly, CDI-specific mortality and complications contributed to failure. find more Relapse rates were similar. Chronic pulmonary disease, ileus, total parenteral nutrition, and duration of tigecycline therapy were predictors of failure. We conclude that severe CDI cases with higher risk for tigecycline monotherapy failure might be identified by contributing factors.Regenerative therapies based on photocrosslinkable hydrogels and stem cells are of growing interest in the field of cartilage repair. Cell-mediated degradation is critical for the successful clinical translation of implanted hydrogels. However, characterising cell-mediated degradation, while simultaneously monitoring the deposition of a distinct new matrix, remains a major challenge. In this study we generated a Fluorescently LAbelled Sensitive Hydrogel (FLASH) to correlate the degradation of a hydrogel bioscaffold with neocartilage formation. Gelatine Methacryloyl (GelMA) was covalently bound to the FITC fluorophore to generate FLASH and bioscaffolds were produced by casting different concentrations of FLASH GelMA, with and without human adipose-derived stem cells (hADSCs) undergoing chondrogenesis. The loss of fluorescence from FLASH bioscaffolds was correlated with changes in mechanical properties, expression of chondrogenic markers and accumulation of a cartilaginous extracellular matrix. The ability of the system to be used as a sensor to monitor bioscaffold degradability during chondrogenesis was evaluated in vitro, in a human ex vivo model of cartilage repair and in a full chondral defect in vivo rabbit model. This study represents a step towards the generation of a high throughput monitoring system to evaluate de novo cartilage formation in tissue engineering therapies.

In vivo PET studies in patients with isolated REM sleep behavior disorder (iRBD) have shown presence of neuroinflammation (microglial activation) in the substantia nigra, and reduced cortical acetylcholinesterase activity, suggestive of cholinergic dysfunction, that was more widespread in patients with poorer cognitive performances. This study aimed to explore whether reduced cortical acetylcholinesterase activity in iRBD is linked to microglial activation in the substantia innominata (SI), the major source of cholinergic input to the cortex.

We used

C(R)-PK11195 and

C-Donepezil PET to assess levels of activated microglia and cholinergic function, respectively, in 19 iRBD patients.

C(R)-PK11195 binding potential (BP

) and

C-Donepezil distribution volume ratio (DVR) values were correlated using the Pearson statistic.

We found that a lower cortical

C-Donepezil DVR correlated with a higher

C(R)-PK11195 BP

in the SI (r=-0.48, p=0.04). At a voxel level, the strongest negative correlations were found in the frontal and temporal lobes.

Our results suggest that reduced cortical acetylcholinesterase activity observed in our iRBD patients could be linked to the occurrence of neuroinflammation in the SI. Early modulation of microglial activation might therefore preserve cortical cholinergic functions in these patients.

Our results suggest that reduced cortical acetylcholinesterase activity observed in our iRBD patients could be linked to the occurrence of neuroinflammation in the SI. Early modulation of microglial activation might therefore preserve cortical cholinergic functions in these patients.

Increasing evidence shows that gut microbiota dysbiosis may play important roles in the occurrence and progression of Parkinson’s disease (PD), but the findings are inconsistent. Besides, the effect of family environment on gut microbiota dysbiosis remains unclear.

We characterized the gut microbial compositions of 63 PD patients, 63 healthy spouses (HS) and 74 healthy people (HP) using 16S rRNA sequencing. Clinical phenotypes and microbial composition were analyzed comprehensively.

There were markedly different microbial compositions among PD, HS and HP samples by alpha/beta diversity. We also found differential microbial compositions among Hoehn & Yahr stage/disease duration. Eight inflammation-associated microbial genera shared a continuously increase trend with increased Hoehn & Yahr stage and disease duration, indicating characteristic bacteria associated with deterioration in PD. Additionally, seven bacterial markers were identified for accurately differentiating PD patients from the controls (area under the curve [AUC] 0.