The influence of training background on difference rate of force calculations during countermovement jump

The aim of this study was to look at differences in countermovement jump (CMJ) performance and selected kinetic parameters in athletes of different training backgrounds and to examine the relationships between these parameters. The subjects were 14 endurance athletes, 12 sprinters, and 13 fire-fighter aspirants (controls); each performed two CMJ on a force plate. The best jump of two attempts was selected and the following parameters were calculated: CMJ height (h), peak power (PP), normalized vertical stiffness (Kvert), rate of force development (RFD), peak RFD (pRFD) during concentric phase, and the ratio between pRFD and the time of its occurrence (iRFD). Sprinters exhibited greater h, PP, Kvert and RFD values than the other groups. A strong correlation was revealed between PP and h, and between pRFD and Kvert in all groups. The magnitude of correlations improved with iRFD when compared to pRFD (.5-.6 vs. .7-.9). There were strong correlations (r>.7) between PP, Kvert, and both pRFD and iRFD only for the endurance athletes group. From these results, it would be recommended to record different RFD calculations during CMJ evaluations, including the new RFD index (iRFD), in athletes of different training backgrounds

The influence of training background on different rate of force development calculations during countermovement jump

The aim of this study was to look at differences in countermovement jump (CMJ) performance and selected kinetic parameters in athletes of different training backgrounds and to examine the relationships between these parameters. The subjects were 14 endurance athletes, 12 sprinters, and 13 fire-fighter aspirants (controls); each performed two CMJ on a force plate. The best jump of two attempts was selected and the following parameters were calculated: CMJ height (h), peak power (PP), normalized vertical stiffness (Kvert), rate of force development (RFD), peak RFD (pRFD) during concentric phase, and the ratio between pRFD and the time of its occurrence (iRFD). Sprinters exhibited greater h, PP, Kvert and RFD values than the other groups. A strong correlation was revealed between PP and h, and between pRFD and Kvert in all groups. The magnitude of correlations improved with iRFD when compared to pRFD (.5-.6 vs. .7-.9). There were strong correlations (r>.7) between PP, Kvert, and both pRFD and iRFD only for the endurance athletes group. From these results, it would be recommended to record different RFD calculations during CMJ evaluations, including the new RFD index (iRFD), in athletes of different training backgrounds

Vertical Jumping as a Monitoring Tool in Endurance Runners: A Brief Review

Jumping performance (e.g., countermovement jump [CMJ]), as a measure of neuromuscular performance, has been suggested as an easy-to-use tool which simultaneously provides neuromuscular and metabolic information and, thereby, allows coaches to confidently monitor the status of their athletes during a workout. This hypothesis has been satisfactorily tested with sprint athletes. However, the rationale for the use of CMJ height loss as an index to monitor the workload during an endurance running session is not sufficiently evidence-based. First, it is assumed that a CMJ height loss occurs during typical interval training for endurance runners. Second, it is also assumed that a significant relationship between metabolic stress and the neuromuscular strain induced during these endurance workouts exists. These two assumptions will be questioned in this review by critically analyzing the kinetics of CMJ performance during and after running workouts, and the relationship between neuromuscular and physiological stress induced during different protocols in endurance runners. The current evidence shows that fatigue induced by common running workouts for endurance runners does not counterbalance the potentiation effect in the CMJ height. Additionally, the findings reported among different studies are consistent regarding the lack of association between CMJ height loss and physiological stress during interval sessions in endurance runners. In practical terms, the authors suggest that this marker of neuromuscular fatigue may not be used to regulate the external training load during running workouts in endurance runners. Nevertheless, the analysis of CMJ height during running workouts may serve to monitor chronic adaptations to training in endurance runners

\u3ci\u3ePASSALUS COARCTATUS\u3c/i\u3e PERCHERON, 1835 (COLEOPTERA: PASSALIDAE): REDESCRIPTION AND NEW DISTRIBUTIONAL RECORDS

Passalus (Passalus) coarctatus Percheron, 1835 was described from Brazil without precise locality data; except for its inclusion in catalogues, nothing is known of this species and only one publication has provided specific locality data. We provide precise localities for P. coarctatus in Trinidad and Tobago, Venezuela, Brazil and Bolivia, we describe the third instar larva, discuss its taxonomic status and correct errors of previous publications. Passalus (Passalus) coarctatus Percheron, 1835 fue descrita de Brasil sin datos precisos de localidad; exceptuando su inclusión en catálogos, no se conoce nada de esta especie y solo un trabajo publicado ha suministrado registros específicos de localidad. Proporcionamos localidades precisas para P. coarctatus en Trinidad y Tobago, Venezuela, Brasil y Bolivia, describimos la larva de tercer estadio, discutimos su estatus taxonómico y enmendamos errores de publicaciones anteriores

Neuromuscular performance of explosive power athletes versus untrained individuals

Electromechanical delay (EMD) and rate of force development (RFD) are determinants of explosive neuromuscular performance. We may expect a contrast in EMD and RFD between explosive power athletes, who have a demonstrable ability for explosive contractions, and untrained individuals. However, this comparison, and the neuromuscular mechanisms for any differences, has not been studied. The neuromuscular performance of explosive power athletes (n = 9) and untrained controls (n = 10) was assessed during a series of twitch, tetanic, explosive and maximum voluntary, isometric knee extensions. Knee extension force and EMG of the superficial quadriceps was measured in three 50 ms time windows from their onset, and normalised to strength and maximal M-wave (Mmax), respectively. Involuntary and voluntary EMD were determined from twitch and explosive voluntary contractions, respectively, and were similar for both groups. The athletes were 28% stronger and their absolute RFD in the first 50 ms was 2-fold that of controls. Athletes had greater normalised RFD (4.86 ± 1.46 vs. 2.81 ± 1.20 MVC.s-1) and neural activation (mean quadriceps, 0.26 ± 0.07 vs. 0.15 ± 0.06 Mmax) during the first 50 ms of explosive voluntary contractions. Surprisingly the controls had a greater normalised RFD in the second 50 ms (6.68 ± 0.92 vs. 7.93 ± 1.11 MVC.s-1) and a greater change in EMG preceding this period. However, there were no differences in the twitch response or normalised tetanic RFD between groups. The differences in voluntary normalised RFD between athletes and controls were explained by agonist muscle neural activation, and not the similar intrinsic contractile properties of the groups

Antimicrobial resistance among migrants in Europe: a systematic review and meta-analysis

BACKGROUND: Rates of antimicrobial resistance (AMR) are rising globally and there is concern that increased migration is contributing to the burden of antibiotic resistance in Europe. However, the effect of migration on the burden of AMR in Europe has not yet been comprehensively examined. Therefore, we did a systematic review and meta-analysis to identify and synthesise data for AMR carriage or infection in migrants to Europe to examine differences in patterns of AMR across migrant groups and in different settings. METHODS: For this systematic review and meta-analysis, we searched MEDLINE, Embase, PubMed, and Scopus with no language restrictions from Jan 1, 2000, to Jan 18, 2017, for primary data from observational studies reporting antibacterial resistance in common bacterial pathogens among migrants to 21 European Union-15 and European Economic Area countries. To be eligible for inclusion, studies had to report data on carriage or infection with laboratory-confirmed antibiotic-resistant organisms in migrant populations. We extracted data from eligible studies and assessed quality using piloted, standardised forms. We did not examine drug resistance in tuberculosis and excluded articles solely reporting on this parameter. We also excluded articles in which migrant status was determined by ethnicity, country of birth of participants' parents, or was not defined, and articles in which data were not disaggregated by migrant status. Outcomes were carriage of or infection with antibiotic-resistant organisms. We used random-effects models to calculate the pooled prevalence of each outcome. The study protocol is registered with PROSPERO, number CRD42016043681. FINDINGS: We identified 2274 articles, of which 23 observational studies reporting on antibiotic resistance in 2319 migrants were included. The pooled prevalence of any AMR carriage or AMR infection in migrants was 25·4% (95% CI 19·1-31·8; I2 =98%), including meticillin-resistant Staphylococcus aureus (7·8%, 4·8-10·7; I2 =92%) and antibiotic-resistant Gram-negative bacteria (27·2%, 17·6-36·8; I2 =94%). The pooled prevalence of any AMR carriage or infection was higher in refugees and asylum seekers (33·0%, 18·3-47·6; I2 =98%) than in other migrant groups (6·6%, 1·8-11·3; I2 =92%). The pooled prevalence of antibiotic-resistant organisms was slightly higher in high-migrant community settings (33·1%, 11·1-55·1; I2 =96%) than in migrants in hospitals (24·3%, 16·1-32·6; I2 =98%). We did not find evidence of high rates of transmission of AMR from migrant to host populations. INTERPRETATION: Migrants are exposed to conditions favouring the emergence of drug resistance during transit and in host countries in Europe. Increased antibiotic resistance among refugees and asylum seekers and in high-migrant community settings (such as refugee camps and detention facilities) highlights the need for improved living conditions, access to health care, and initiatives to facilitate detection of and appropriate high-quality treatment for antibiotic-resistant infections during transit and in host countries. Protocols for the prevention and control of infection and for antibiotic surveillance need to be integrated in all aspects of health care, which should be accessible for all migrant groups, and should target determinants of AMR before, during, and after migration. FUNDING: UK National Institute for Health Research Imperial Biomedical Research Centre, Imperial College Healthcare Charity, the Wellcome Trust, and UK National Institute for Health Research Health Protection Research Unit in Healthcare-associated Infections and Antimictobial Resistance at Imperial College London

Comparison of seven prognostic tools to identify low-risk pulmonary embolism in patients aged <50 years

publishersversionPeer reviewe

Association of Candidate Gene Polymorphisms With Chronic Kidney Disease: Results of a Case-Control Analysis in the Nefrona Cohort

Chronic kidney disease (CKD) is a major risk factor for end-stage renal disease, cardiovascular disease and premature death. Despite classical clinical risk factors for CKD and some genetic risk factors have been identified, the residual risk observed in prediction models is still high. Therefore, new risk factors need to be identified in order to better predict the risk of CKD in the population. Here, we analyzed the genetic association of 79 SNPs of proteins associated with mineral metabolism disturbances with CKD in a cohort that includes 2, 445 CKD cases and 559 controls. Genotyping was performed with matrix assisted laser desorption ionizationtime of flight mass spectrometry. We used logistic regression models considering different genetic inheritance models to assess the association of the SNPs with the prevalence of CKD, adjusting for known risk factors. Eight SNPs (rs1126616, rs35068180, rs2238135, rs1800247, rs385564, rs4236, rs2248359, and rs1564858) were associated with CKD even after adjusting by sex, age and race. A model containing five of these SNPs (rs1126616, rs35068180, rs1800247, rs4236, and rs2248359), diabetes and hypertension showed better performance than models considering only clinical risk factors, significantly increasing the area under the curve of the model without polymorphisms. Furthermore, one of the SNPs (the rs2248359) showed an interaction with hypertension, being the risk genotype affecting only hypertensive patients. We conclude that 5 SNPs related to proteins implicated in mineral metabolism disturbances (Osteopontin, osteocalcin, matrix gla protein, matrix metalloprotease 3 and 24 hydroxylase) are associated to an increased risk of suffering CKD

Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study

Background: Approximately 450 000 children are born with familial hypercholesterolaemia worldwide every year, yet only 2·1% of adults with familial hypercholesterolaemia were diagnosed before age 18 years via current diagnostic approaches, which are derived from observations in adults. We aimed to characterise children and adolescents with heterozygous familial hypercholesterolaemia (HeFH) and understand current approaches to the identification and management of familial hypercholesterolaemia to inform future public health strategies. Methods: For this cross-sectional study, we assessed children and adolescents younger than 18 years with a clinical or genetic diagnosis of HeFH at the time of entry into the Familial Hypercholesterolaemia Studies Collaboration (FHSC) registry between Oct 1, 2015, and Jan 31, 2021. Data in the registry were collected from 55 regional or national registries in 48 countries. Diagnoses relying on self-reported history of familial hypercholesterolaemia and suspected secondary hypercholesterolaemia were excluded from the registry; people with untreated LDL cholesterol (LDL-C) of at least 13·0 mmol/L were excluded from this study. Data were assessed overall and by WHO region, World Bank country income status, age, diagnostic criteria, and index-case status. The main outcome of this study was to assess current identification and management of children and adolescents with familial hypercholesterolaemia. Findings: Of 63 093 individuals in the FHSC registry, 11 848 (18·8%) were children or adolescents younger than 18 years with HeFH and were included in this study; 5756 (50·2%) of 11 476 included individuals were female and 5720 (49·8%) were male. Sex data were missing for 372 (3·1%) of 11 848 individuals. Median age at registry entry was 9·6 years (IQR 5·8-13·2). 10 099 (89·9%) of 11 235 included individuals had a final genetically confirmed diagnosis of familial hypercholesterolaemia and 1136 (10·1%) had a clinical diagnosis. Genetically confirmed diagnosis data or clinical diagnosis data were missing for 613 (5·2%) of 11 848 individuals. Genetic diagnosis was more common in children and adolescents from high-income countries (9427 [92·4%] of 10 202) than in children and adolescents from non-high-income countries (199 [48·0%] of 415). 3414 (31·6%) of 10 804 children or adolescents were index cases. Familial-hypercholesterolaemia-related physical signs, cardiovascular risk factors, and cardiovascular disease were uncommon, but were more common in non-high-income countries. 7557 (72·4%) of 10 428 included children or adolescents were not taking lipid-lowering medication (LLM) and had a median LDL-C of 5·00 mmol/L (IQR 4·05-6·08). Compared with genetic diagnosis, the use of unadapted clinical criteria intended for use in adults and reliant on more extreme phenotypes could result in 50-75% of children and adolescents with familial hypercholesterolaemia not being identified. Interpretation: Clinical characteristics observed in adults with familial hypercholesterolaemia are uncommon in children and adolescents with familial hypercholesterolaemia, hence detection in this age group relies on measurement of LDL-C and genetic confirmation. Where genetic testing is unavailable, increased availability and use of LDL-C measurements in the first few years of life could help reduce the current gap between prevalence and detection, enabling increased use of combination LLM to reach recommended LDL-C targets early in life