Strength and isometric torque control in individuals with Parkinson’s disease

It has been previously reported that patients with Parkinson’s disease (PD) struggle with fine adjustments of finger forces while manipulating an object. However, impairments in everyday activities can not only be attributed to difficulties with the linear forces applied on an object, but also to the application of rotational forces (torque). This study examined finger strength and isometric torque control in elderly persons with PD. Six individuals with PD (66.1 ± 0.7 years), six elderly healthy controls (65.3 ± 0.2 years) matched by age, gender and handedness, and six young adults (22.3 ± 0.2 years) participated in this study. The subjects were asked to perform two tasks: maximum voluntary thumb-index pinching torque production (MVT) and constant isometric thumb-index torque control at 40% of their MVT for 20 s. The results showed decreased strength and increased difficulty in isometric torque control in individuals with PD as compared to their healthy peers. This study demonstrates that PD affects isometric finger torque production and control. An erratum to this article can be found at     

Influence of muscle architecture on the torque and power–velocity characteristics of young and elderly men

This study investigated the contribution of muscle architecture to the differences in the torque–velocity and power–velocity relationships between older (OM n = 9, aged 69–82 years) and younger men (YM n = 15, aged 19–35 years). Plantarflexors’ (PF) maximal isometric and concentric torques were recorded at 0.87, 1.75, 2.62, 3.49 and 4.36 rad s⁻¹. Physiological cross-sectional area (PCSA) was calculated as the ratio of muscle volume (determined by magnetic resonance imaging) to muscle fascicle length (L _f, measured by ultrasonography). GM PCSA and L _f of the OM were, respectively, 14.3% (P < 0.05) and 19.3% (P < 0.05) smaller than of the YM. In the OM, GM maximum isometric torque and maximum contraction velocity (V _max), estimated from Hill’s equation were, respectively, 48.5 and 38.2% lower (P < 0.001) than in the YM. At all contraction velocities, the OM produced less torque than the YM (46.3% of YM at 0.87 rad s⁻¹ to 14.7% at 4.36 rad s⁻¹, P < 0.001). Peak power (PP) of the OM was 80% lower than that of the YM and normalisation of PP to muscle volume only reduced this difference by 10%. Normalisation of torque to PCSA reduced, but did not eliminate, differences in torque between YM and OM (9.6%) and differences in torque/PCSA increased with contraction velocity (P < 0.05). After normalisation of velocity to L _f, the difference in V _max between the OM and the YM was reduced to 15.9%. Thus, although muscle architecture contributes significantly to the differences in the torque– and power–velocity properties of OM and YM, other contractile factors, intrinsic to the muscle, seem to play a role. It is noteworthy that the deficit in PP between OM and YM is far greater than that of muscle torque, even after normalisation of PP to muscle volume. This finding likely plays an important role in the loss of mobility in old age.     

High prevalence of torque teno sus virus in China and genetic diversity of the 5’ non-coding region

Members of the family Anelloviridae are emerging circular DNA viruses infecting many species of vertebrates including pigs. To date, members of two distinct genera, Iotatorquevirus, including torque teno sus virus 1a and torque teno sus virus 1b (TTSuV1a and TTSuV1b), and Kappatorquevirus, including torque teno sus virus k2a and torque teno sus virus k2b (TTSuVk2a and TTSuVk2b), have been identified in domestic pigs and wild boars. The goal of this study was to evaluate the prevalence and genetic diversity of these viruses based on 5’ non-coding genes in Chinese swine herds experiencing clinical symptoms. One hundred eighty-five clinical samples from 11 different regions, collected during 2008-2009, were analyzed using a PCR method, and the results revealed a high TTSuV-positive rate of 78.9 % (146/185) in pigs. Moreover, we detected co-infection with multiple TTSuV strains in the same pig. Nucleotide sequencing results revealed greater genetic diversity within the genus Kappatorquevirus than within the genus Iotatorquevirus. In addition, TTSuVk2b, a novel virus discovered in New Zealand in 2012, was also identified in this study. In summary, the present work helps us obtain more knowledge about the epidemiology and genetic diversity of TTSuVs.     

Effects of 17 days bedrest on the maximal voluntary isometric torque and neuromuscular activation of the plantar and dorsal flexors of the ankle

Maximal voluntary isometric torque values of the ankle plantar (T _im,_PF) and dorsal flexors (T _im,_DF) were assessed in eight healthy adult males at 5° and 15° of dorsal flexion (DF) and at 5°, 15° and 25° of plantar flexion (PF) with the knee at right angles, before (two times), during (three times) and after (three times) 17 days of 6° head-down tilt bedrest (BR). Integrated electromyograms (iEMG) were also recorded from the gastrocnemius medialis and tibialis anterior. T _im,_PF and the iEMG of the gastrocnemius medialis were significantly larger (by 14% and by 27%, respectively) at the end of recovery than before BR. This was probably the consequence of training and/or habituation leading to: (1) increased activation of the plantar flexors; and (2) decreased co-activation of the antagonist muscles. Neither T _im,_DF nor the tibialis anterior iEMG changed significantly. The effects of BR on muscle performance were evaluated as follows. The net torque generated by a given muscle group was assumed to be the algebraic sum of the torque generated by the agonists and by the antagonists. Thus, for the plantar flexors T_im,PF=αiEMG_Gm − βiEMG_Ta, where: (1) iEMG_Gm and iEMG_Ta are the iEMGs of gastrocnemius medialis and of tibialis anterior during maximal PF; and (2) the constants α and β represent the electromechanical coupling of the plantar (α) and dorsal (β) flexors. Similarly for the dorsal flexors: T_im,DF=βiEMG_Ta − αiEMG_Gm, where iEMG_Ta and iEMG_Gm are the iEMGs of tibialis anterior and gastrocnemius medialis during maximal DF. Torque and iEMG values were assessed for all subjects under all experimental conditions. Thus, since the biomechanical leverage of the system was constant, α and β could be calculated. During BR, α decreased by 25% and it dropped by a further 30% during recovery. In contrast, β remained almost unchanged. This suggests that, in spite of training and/or habituation, BR significantly impaired the maximal isometric performance of the plantar flexors, an effect that continued during the initial 10 days of recovery. Accepted: 4 February 2000