Abstract: Background The Millennium Declaration in 2000 brought special global attention to HIV, tuberculosis and malaria through the formulation of Millennium Development Goal 6 (MDG 6). The Global Burden of Disease 2013 study provides a consistent and comprehensive approach to disease estimation 1990 to 2013, and an opportunity to assess if there has been accelerated progress since the Millennium Declaration. Methods To estimate incidence and mortality for HIV, we used the UNAIDS Spectrum model appropriately modified based on a systematic review of the literature on mortality with and without out antiretroviral therapy (ART). For concentrated epidemics, we calibrated Spectrum models to fit vital registration data corrected for misclassification of HIV deaths. In generalized epidemics, we minimized a loss function to select epidemic curves most consistent with prevalence data and demographic data on all-cause mortality. We analyzed counterfactual scenarios for HIV to assess years of life saved through prevention of mother to child transmission (PMTCT) and anti-retroviral therapy (ART). For tuberculosis, we analyzed vital registration and verbal autopsy data to estimate mortality using cause of death ensemble modeling. We analyzed data on corrected case-notifications, expert opinions on the case-detection rate, prevalence surveys and estimated cause-specific mortality using Bayesian metaregression to generate consistent trends in all parameters. Malaria mortality and incidence were analyzed using an updated cause of death database, a systematic analysis of verbal autopsy validation studies for malaria and recent literature on incidence, drug resistance and coverage of insecticide treated bed nets. Findings Globally in 2013, there were 1.8 million new HIV infections (95% uncertainty interval 1.7 million to 2.1 million), 29.0 million prevalent HIV cases (27.9 to 31.4) and 1.3 million HIV deaths (1.2 to 1.5). At the peak of the epidemic in 2005, HIV caused 1.7 million deaths (1.6 to 1.9). Concentrated epidemics in Latin America and Eastern Europe are substantially smaller than previously estimated. Through interventions including PMTCT and ART, 19.3 million life years have been saved, 68.9% in the developing world. From 2000 to 2011, the ratio of development assistance for health for HIV to years of life saved through intervention was $4,647-$7,137 in the developing world. All-forms tuberculosis (including Individuals who are HIV-positive) incidence, prevalence and death numbers in 2013 were 6.6 million (6.4 to 6.7), 10.1 million (9.8 to 10.4) and 1.4 million (1.3 to 1.5), the same figures in Individuals who are HIV-negative were 6.1 million (6.0 to 6.3), 9.5 million (9.2 to 9.8) and 1.3 million
Many studies in Western societies have shown that women prefer relatively taller men as potential partners, whereas men prefer women who are slightly shorter than themselves. Here, we discuss possible limitations of previous results within the context of the stimuli used (i.e., differences in the perceived body size of female silhouettes). Our results show that, at least in a Polish sample (N= 231), modified stimuli did not essentially change the observed male-taller preferences. In contrast, we report height preferences in a traditional ethnic group, the Datoga people from Tanzania (N= 107), in which men and women preferred extreme sexual dimorphism in stature (SDS) sets (i.e., men and women chose women much taller or much shorter than themselves). Thus, our data do not accord with the suggestion of a universal preference for taller men, but rather suggests that height preferences may be influenced by cultural, environmental, and ecological conditions.
Interaction between transmembrane helices often determines biological activity of membrane proteins. Bitopic proteins, a broad subclass of membrane proteins, form dimers containing two membrane-spanning helices. Some aspects of their structure-function relationship cannot be fully understood without considering the protein-lipid interaction, which can determine the protein conformational ensemble. Experimental and computer modeling data concerning transmembrane parts of bitopic proteins are reviewed in the present paper. They highlight the importance of lipid-protein interactions and resolve certain paradoxes in the behavior of such proteins. Besides, some properties of membrane organization provided a clue to understanding of allosteric interactions between distant parts of proteins. Interactions of these kinds appear to underlie a signaling mechanism, which could be widely employed in the functioning of many membrane proteins. Treatment of membrane proteins as parts of integrated fine-tuned proteolipid system promises new insights into biological function mechanisms and approaches to drug design. This article is part of a Special Issue entitled: Lipid order/lipid defects and lipid-control of protein activity edited by Dirk Schneider.