35 research outputs found
Right Ventricular Adaptation Is Associated with the Glu298Asp Variant of the NOS3 Gene in Elite Athletes
Nitric oxide (NO), an important endogenous pulmonary vasodilator is synthetized by the endothelial NO synthase (NOS3). Reduced NO bioavailability and thus the Glu298Asp polymorphism of NOS3 may enhance right ventricular (RV) afterload and hypertrophic remodeling and influence athletic performance. To test this hypothesis world class level athletes (water polo players, kayakers, canoeists, rowers, swimmers, n = 126) with a VO2 maximum greater than 50ml/kg/min were compared with non-athletic volunteers (n = 155). Cardiopulmonary exercise tests and cardiac magnetic resonance imaging (cMRI) were performed to determine structural or functional changes. Genotype distribution of the NOS3 Glu298Asp polymorphism was not affected by gender or physical performance. Cardiac MRI showed increased stroke volume with eccentric hypertrophy in all athletes regardless of their genotype. However, the Asp allelic variant carriers had increased RV mass index (32+/-6g versus 27+/-6g, p<0.01) and larger RV stroke volume index (71+/-10ml versus 64+/-10ml, p<0.01) than athletes with a Glu/Glu genotype. Genotype was not significantly associated with athletic performance. In the non-athletic group no genotype related differences were detected. The association between the NOS3 Glu298Asp polymorphism and RV structure and dimension in elite athletes emphasizes the importance of NOS3 gene function and NO bioavailability in sport related cardiac adaptation
Global assessment of marine plastic exposure risk for oceanic birds
Plastic pollution is distributed patchily around the worldâs oceans. Likewise, marine organisms that are vulnerable to plastic ingestion or entanglement have uneven distributions. Understanding where wildlife encounters plastic is crucial for targeting research and mitigation. Oceanic seabirds, particularly petrels, frequently ingest plastic, are highly threatened, and cover vast distances during foraging and migration. However, the spatial overlap between petrels and plastics is poorly understood. Here we combine marine plastic density estimates with individual movement data for 7137 birds of 77 petrel species to estimate relative exposure risk. We identify high exposure risk areas in the Mediterranean and Black seas, and the northeast Pacific, northwest Pacific, South Atlantic and southwest Indian oceans. Plastic exposure risk varies greatly among species and populations, and between breeding and non-breeding seasons. Exposure risk is disproportionately high for Threatened species. Outside the Mediterranean and Black seas, exposure risk is highest in the high seas and Exclusive Economic Zones (EEZs) of the USA, Japan, and the UK. Birds generally had higher plastic exposure risk outside the EEZ of the country where they breed. We identify conservation and research priorities, and highlight that international collaboration is key to addressing the impacts of marine plastic on wide-ranging species
Global assessment of marine plastic exposure risk for oceanic birds
Plastic pollution is distributed patchily around the worldâs oceans. Likewise, marine organisms that are vulnerable to plastic ingestion or entanglement have uneven distributions. Understanding where wildlife encounters plastic is crucial for targeting research and mitigation. Oceanic seabirds, particularly petrels, frequently ingest plastic, are highly threatened, and cover vast distances during foraging and migration. However, the spatial overlap between petrels and plastics is poorly understood. Here we combine marine plastic density estimates with individual movement data for 7137 birds of 77 petrel species to estimate relative exposure risk. We identify high exposure risk areas in the Mediterranean and Black seas, and the northeast Pacific, northwest Pacific, South Atlantic and southwest Indian oceans. Plastic exposure risk varies greatly among species and populations, and between breeding and non-breeding seasons. Exposure risk is disproportionately high for Threatened species. Outside the Mediterranean and Black seas, exposure risk is highest in the high seas and Exclusive Economic Zones (EEZs) of the USA, Japan, and the UK. Birds generally had higher plastic exposure risk outside the EEZ of the country where they breed. We identify conservation and research priorities, and highlight that international collaboration is key to addressing the impacts of marine plastic on wide-ranging species
THE FRACTION OF EXALED NITRIC OXIDE IN THE MONITORING OF ASTHMA THERAPY: PRELIMINARY CONSIDERATIONS.
TNF-Alpha Levels in Tears: A Novel Biomarker to Assess the Degree of Diabetic Retinopathy
We assess the level of tumour necrosis factor alpha (TNF-alpha) in tear fluids and other serum
parameters associated with diabetes in different degrees of diabetic retinopathy. We have performed a prospective,
nonrandomized, observational study. Study population consisted of 16 healthy subjects (controls) and 32 type 2
diabetic patients: 16 affected by proliferative diabetic retinopathy (PDR) and 16 with nonproliferative retinopathy
(NDPR, background/preproliferative). Body mass index, urinary albumin, blood glucose, HbA1c, and tear levels
of TNF-alpha were measured in all subjects. The value of glycaemia, microalbuminurea, and Body mass index
in diabetic retinopathy groups were higher than those in control group ().
Glycemia in NPDR: 6.6âmmol/L (range: 5.8â6.3); in PDR: 6.7âmmol/L
(range: 6.1â7.2); in control: 5.7âmmol/L (range: 4.9â6.1); microalbuminurea in
NPDR: 10.6âmg/L (range: 5.6â20); in PDR: 25.2âmg/L
(range: 17â40); in control: 5.3âmg/L (range: 2.6â10); Body mass index in
NPDR: 26âKg/m2 (range: 20.3â40);
in PDR: 28âKg/m2 (range 20.3â52);
in control: 21âKg/m2 (range 19â26).
The TNF-alpha concentrations in tears increase with the severity of pathology
and were lower in control group than in diabetic subjects. In the end, the level of TNF-alpha
is highly correlated with severity of diabetic retinopathy and with nephropathy.
Tear fluid collection may be a useful noninvasive method for the detection of proliferative diabetic retinopathy