Dietary flavonoids are associated with health benefits, including improved cognitive function and reduced risks associated with aging, such as the risk of dementia. Flavonoids, or the subclass flavanols, are present in green tea, red wine, cocoa, and some fruits. Evidence has also shown that flavanols are linked to lower blood pressure due to vasodilation in the peripheral vasculature and brain. The author conducted a study in which he used chocolate consumption as a surrogate for flavonoid consumption and determined whether there is an association between a population’s cognitive function and chocolate intake. As a surrogate marker for cognitive function for a given country, the author used the total number of Nobel laureates per capita, with the assumption that this reflected the proportion of people in the country with superior intelligence. The study concluded that there was a close significant linear correlation between chocolate consumption per capita and the number of Nobel laureates per 10 million people in 23 countries. The only outlier was Sweden, with more Nobel laureates than predicted based on chocolate consumption. Switzerland ranked first with regard to chocolate consumption and number of Nobel laureates. The author noted that based on the slope of the regression line, chocolate consumption would need to increase by 0.4 kg of chocolate per capita per year to increase the number of Nobel laureates. Therefore, in the United States, the population would need to consume an additional 125 million kg of chocolate per year to increase the number of Nobel laureates by one. There are many limitations to the interpretation of this study, including the cause versus effect of chocolate consumption.
Messerli FH. Chocolate consumption, cognitive function, and Nobel laureates. N Engl J Med. 2012;367:1562–1564.
Correspondence information not provided.
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Vitamin D has been associated with the development of autoimmune diseases, such as type 1 diabetes mellitus. Vitamin D is produced in the skin by ultraviolet B radiation and 25-hydroxy vitamin D (25OHD), which is a serum marker for vitamin D concentrations. Some studies have shown an association between low serum 25OHD concentrations and type 1 diabetes mellitus (T1DM), and others have shown an inverse relationship between latitude and the incidence of T1DM. The authors conducted a case-control study in Australia, a sub-tropical environment with abundant sunlight, to determine if children with T1DM have lower serum vitamin D compared to children without T1DM. They studied 56 children with T1DM (14 newly diagnosed) and 46 unrelated control subjects and measured serum 25OHD and 1,25-dihydroxy vitamin D (1,25(OH)2D). They also genotyped in each participant the vitamin D receptor polymorphisms Tqa1, Fok1, and Apa1. These vitamin D receptor polymorphisms were shown in previous studies to influence susceptibility to T1DM. The authors also collected data on the Fitzpatrick skin classification, self-reported daily hours of outdoor exposure, and mean ultraviolet index over a 35-day period. They found that serum 25OHD levels were lower in children with T1DM versus controls. The children with T1DM also had lower self-reported outdoor exposure and mean ultraviolet exposure, and there was no significant difference in distribution of vitamin D receptor polymorphisms. The children with newly diagnosed T1DM had lower 1,25(OH)2D than did controls or children with established diabetes. The authors concluded that low concentrations of vitamin D associated with T1DM are found even in environments with abundant sunlight. They noted, however, that it is unknown if vitamin D is a risk factor or consequence of T1DM.
Greer RM, Portelli SL, Hung BSM, et al. Serum vitamin D levels are lower in Australian children and adolescents with type 1 diabetes than in children without diabetes. Pediatr Diabetes. 2012;1–111.
Correspondence: Dr. Ristan M. Greer at firstname.lastname@example.org
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Glioblastoma multiforme is the most common and most malignant of the primary brain tumors. There has been recent interest in use of immunotherapy, or vaccines targeted against the tumor, as a therapy for glioblastoma multiforme (GBM). The authors reported on an open-label, single-institution, phase-one study that evaluated a new autologous vaccine, ICT-107, for safety and response in patients with GBM or brain-stem glioma. The ICT-107 vaccine targeted antigens that were overexpressed on cancer stem cells and other tumor-specific antigens. These tumor-associated antigens on GBM and cancer stem cells included Her2/neu, TRP-2, AIM-2, gp100, MAGE-1, and IL13Rα2. The vaccine was created using patient dendritic cells obtained through leukapheresis collection. Because dendritic cells are the most potent antigen-presenting cells, they were pulsed with synthetic class-one peptides from the tumor-specific antigens. Following culturing of the dendritic cells with the peptides, the vaccination was give to the patients and immune response was monitored. Study results showed that the 16 newly diagnosed adult GBM patients had a progression-free survival rate of 16.9 months, two-year survival rate of 43.8 percent (95 percent confidence interval [CI], 19.8–66.0), and overall three-year survival rate of 55.6 percent (95 percent CI, 28.6–75.9). Six patients showed no tumor recurrence at 49 to 66 months. Four ICT-107–targeted antigens in the pre-vaccine tumors correlated with prolonged progression-free and overall survival rates. The dendritic cell vaccine did not exhibit toxicity in this study. The authors concluded that this phase-one study of ICT-107 demonstrated the safety, feasibility, and bioactivity of a dendritic cell vaccine for GBM patients. A phase-two randomized controlled trial is underway.
Phuphanich S, Wheeler CJ, Rudnick JD, et al. Phase 1 trial of a multi-epitope-pulsed dendritic cell vaccine for patients with newly diagnosed glioblastoma. Cancer Immunol Immunother. 2012. doi:10.1007/s00262–012–1319–0.
Correspondence: S. Phuphanich at email@example.com and C. J. Wheeler at firstname.lastname@example.org
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Clinical pathology abstracts editors: Deborah Sesok-Pizzini, MD, MBA, associate professor, Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, and medical director, Blood Bank and Transfusion Medicine, Children’s Hospital of Philadelphia; Tina Ipe, MD, MPH, resident, Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania.