Influence of Changes in Body Weight on Peak Vertical Force in Osteoarthritic Dogs: A Possible Bias in Study Outcome

Objective— Force platform gait analysis is a recognized clinical evaluation tool that captures and documents the in vivo pathomechanics of osteoarthritis (OA). In a clinical trial designed to evaluate the impact of 2 specific diets, an increase in body weight (BW) was observed in lame client-owned dogs. Covariance analysis was used to evaluate the interference of BW changes toward the evolution of peak vertical force (PVF) values. These secondary findings are reported in this study.
Study Design— Prospective study.
Animals— Lame dogs (n=26).
Methods— Dogs with radiographic evidence of OA and low PVF values were fed with 2 specific diets for 30 and 60 days. PVF and BW were recorded at baseline, day 30 (D30), and D90.
Results— Mean (±SD) PVF values (%BW) did not differ significantly over time (D0: 63.9±17.2; D30: 65.5±17.4; and D90: 66.5±20.1). In contrast, BW (kg) was significantly higher at D90 (41.3±7.9) when compared with D30 (39.9±8.4) and D0 (40.0±8.7). Upon covariance analyses, BW changes interfere significantly with PVF values already normalized in %BW ( P =.013). Values of PVF adjusted using BW as a covariate were then 63.4±17.1 (D0), 65.0±17.3 (D30), and 67.6±20.5 (D90), whereas D90 was significantly higher than D0.
Conclusion— These findings highlighted the interference of changes in BW toward locomotor function of OA dogs when using PVF values normalized in %BW. Exacerbation of lameness when a gain in BW occurred was also sustained, raising a possible bias in clinical study outcomes.
Clinical Relevance— A BW increase in dogs with OA could exacerbate a preexisting lameness and induce a bias in clinical trials.     

Fluctuations in European eel (Anguilla anguilla) recruitment resulting from environmental changes in the Sargasso Sea

European eel decline is now widely observed and involves a large number of factors such as overfishing, pollution, habitat loss, dam construction, river obstruction, parasitism and environmental changes. In the present study, we analyzed the influence of environmental conditions in the Sargasso Sea and Atlantic ocean circulation on European glass eel recruitment success. Over a recent 11‐yr period, we showed a strong positive correlation between an original index of glass eel recruitment and primary production (PP) in eel spawning area. Moreover, PP was negatively correlated with temperature in the Sargasso Sea. Therefore, we used sea temperature as an inverse proxy of marine production. A close negative relationship has been found over the last four decades between long‐term fluctuations in recruitment and in sea temperature. These findings were reinforced by the detection of a regime shift in sea temperature that preceded the start of the decline in glass eel recruitment in the early 1980s. By contrast, variations in integrative indices measuring ocean circulation, i.e. latitude and strength of the Gulf Stream, did not seem to explain variations in glass eel recruitment. Our results support the hypothesis of a strong bottom‐up control of leptocephali survival and growth by PP in the Sargasso Sea on short and long time scales. We argue that sea warming in the eel spawning area since the early 1980s has modified marine production and eventually affected the survival rate of European eels at early life stages.     

How fast can the European eel (Anguilla anguilla) larvae cross the Atlantic Ocean?

The migration duration of European eel ( Anguilla anguilla ) larvae (leptocephali) from the spawning areas in the Sargasso Sea to the European continental shelf remains highly controversial, with estimates varying from 6 months to more than 2 yr. We estimated the fastest migration period and the shortest distance travelled by eel larvae by simulating Lagrangian particles released in the Sargasso Sea and by simulating a range of larval behaviours (fixed-depth drift, vertical diurnal migration and active-depth selection to maximize current velocity). This enabled us to compute (i) a passive drift speed, and (ii) a hypothetic swimming speed needed for European eel larvae to cross the Atlantic in 6 months (i.e., the migration duration estimated from otolith daily growth increments). Our results show that the minimum travel time for an eel larva that is passively drifting was 10 months and 3 days. Active behaviours (vertical diurnal migration and rheotaxis) paradoxically increased the migration period. We found that for leptocephali to cross the Atlantic Ocean in 6 months, they would need to swim a minimum of 3.4 body lengths per second for 8200 km. No larvae have been observed with such swimming capabilities. These results provide evidence that leptocephali cannot cross the Atlantic in 6 months.