This 48-week, randomized, placebo-controlled phase 3 study (DMD114044; NCT01254019) evaluated efficacy and safety of subcutaneous drisapersen 6 mg/kg/week in 186 ambulant boys aged ≥5 years, with Duchenne muscular dystrophy (DMD) resulting from an exon 51 skipping amenable mutation. Drisapersen was generally well tolerated, with injection-site reactions and renal events as most commonly reported adverse events. A nonsignificant treatment difference (P = 0.415) in the change from baseline in six-minute walk distance (6MWD; primary efficacy endpoint) of 10.3 meters in favor of drisapersen was observed at week 48. Key secondary efficacy endpoints (North Star Ambulatory Assessment, 4-stair climb ascent velocity, and 10-meter walk/run velocity) gave consistent findings. Lack of statistical significance was thought to be largely due to greater data variability and subgroup heterogeneity. The increased standard deviation alone, due to less stringent inclusion/exclusion criteria, reduced the statistical power from pre-specified 90% to actual 53%. Therefore, a post-hoc analysis was performed in 80 subjects with a baseline 6MWD 300-400 meters and ability to rise from floor. A statistically significant improvement in 6MWD of 35.4 meters (P = 0.039) in favor of drisapersen was observed in this subpopulation. Results suggest that drisapersen could have benefit in a less impaired population of DMD subjects.
Community-acquired pneumonia (CAP) is amongst the leading causes of death worldwide.
As inflammatory markers, cytokines can predict outcomes, if interpreted together with
clinical data and scoring systems such as CURB-65, CRB, and Acute Physiology and
Chronic Health Evaluation II (APACHE II). The aim of this study was to determine the
impact of inflammatory biomarkers on the early mortality of hospitalized CAP
patients. Twenty-seven CAP patients needing hospitalization were enrolled for the
study and samples of interleukin-1 (IL-1) and interleukin-6 (IL-6), tumor necrosis
factor alpha (TNF-α), C-reactive protein (CRP), and homocystein were collected at the
time of admission (day 1) as well as on the seventh day of the treatment. There was a
significant reduction in the levels of IL-6 between the first and the second
collections. Median IL-6 values decreased from 24 pg/mL (day 1) to 8 pg/mL (day 7)
(P=0.016). The median levels of TNF-α were higher in patients: i) with acute kidney
injury (AKI) (P=0.045), ii) requiring mechanical ventilation (P=0.040), iii) with
short hospital stays (P=0.009), iv) admitted to the intensive care unit (ICU)
(P=0.040), v) who died early (P=0.003), and vi) with worse CRB scores (P=0.013). In
summary, IL-6 and TNF-α levels were associated with early mortality of CAP patients.
Longer admission levels demonstrated greater likelihood of early death and overall
mortality, necessity of mechanical ventilation, and AKI.
Recent studies showed that most cells have receptors and enzymes responsible for metabolism of vitamin D. Several diseases have been linked to vitamin D deficiency, such as hypertension, diabetes, depression, Alzheimer's disease, Parkinson's disease, multiple sclerosis, and chronic pain syndromes such as fibromyalgia. The association between fibromyalgia and vitamin D deficiency is very controversial in the literature with conflicting studies and methodological problems, which leads to more questions than answers. The purpose of this article is to raise questions about the association of hypovitaminosis D with fibromyalgia considering causal relationships, treatment, and pathophysiological explanations.
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