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1.
J Nutr Health Aging ; 27(1): 67-74, 2023.
Article in English | MEDLINE | ID: mdl-36651488

ABSTRACT

OBJECTIVES: To investigate associations between nutrition risk (determined by SCREEN-II) and malnutrition (diagnosed by the GLIM criteria) with five-year mortality in Maori and non-Maori of advanced age. DESIGN: A longitudinal cohort study. SETTING: Bay of Plenty and Lakes regions of New Zealand. PARTICIPANTS: 255 Maori; 400 non-Maori octogenarians. MEASUREMENTS: All participants were screened for nutrition risk using the Seniors in the Community: Risk Evaluation for Eating and Nutrition (SCREEN-II). Those at high nutrition risk (SCREEN-II score <49) had the Global Leadership Initiative in Malnutrition (GLIM) criteria applied to diagnose malnutrition or not. Demographic, physical and health characteristics were obtained by trained research nurses using a standardised questionnaire. Five-year mortality was calculated from Government data. The association of nutrition risk (SCREEN-II) and a malnutrition diagnosis (GLIM) with five-year mortality was examined using logistic regression and cox proportional hazard models of increasing complexity. RESULTS: 56% of Maori and 46% of non-Maori participants had low SCREEN-II scores indicative of nutrition risk. The prevalence of GLIM diagnosed malnutrition was lower for both Maori and non-Maori (15% and 19% of all participants). Approximately one-third of participants (37% Maori and 32% non-Maori) died within the five-year follow-up period. The odds of death for both Maori and non-Maori was significantly lower with greater SCREEN II scores (better nutrition status), (OR (95% CI); 0.58 (0.38, 0.88), P < 0.05 and 0.53 (0.38, 0.75), P < 0.001, respectively). GLIM diagnosed malnutrition was not significantly associated with five-year mortality for Maori (OR (95% CI); 0.88 (0.41, 1.91), P >0.05) but was for non-Maori. This association remained significant after adjustment for other predictors of death (OR (95% CI); 0.50 (0.29, 0.86), P< 0.05). Reduced food intake was the only GLIM criterion predictive of five-year mortality for Maori (HR (95% CI); 10.77 (4.76, 24.38), P <0.001). For non-Maori, both aetiologic and phenotypic GLIM criteria were associated with five-year mortality. CONCLUSION: Nutrition risk, but not malnutrition diagnosed by the GLIM criteria was significantly associated with mortality for Maori. Conversely, both nutrition risk and malnutrition were significantly associated with mortality for non-Maori. Appropriate phenotypic criteria for diverse populations are needed within the GLIM framework.


Subject(s)
Leadership , Malnutrition , Aged, 80 and over , Humans , Cohort Studies , Longitudinal Studies , New Zealand/epidemiology , Malnutrition/diagnosis , Malnutrition/epidemiology , Nutritional Status , Nutrition Assessment
2.
Sci Rep ; 8(1): 13943, 2018 09 17.
Article in English | MEDLINE | ID: mdl-30224772

ABSTRACT

Soiling by dry deposition affects the power output of photovoltaic (PV) modules, especially under dry and arid conditions that favor natural atmospheric aerosols (wind-blown dust). In this paper, we report on measurements of the soiling effect on the energy yield of grid-connected crystalline silicon PV modules deployed in five cities across a north-south transect of approximately 1300 km in the Atacama Desert ranging from latitude 18°S to latitude 30°S. Energy losses were assessed by comparing side-by-side outputs of four co-planar PV modules. Two of the PV modules of the array were kept clean as a control, while we allowed the other two to naturally accumulate soiling for 12 months (from January 2017 to January 2018). We found that the combination of high deposition rates and infrequent rainfalls led to annual energy losses that peaked at 39% in the northern coastal part of the desert. In contrast, annual energy losses of 3% or less were measured at relatively high-altitude sites and also at locations in the southern part of the desert. For comparison, soiling-induced annual energy losses of about 7% were measured in Santiago, Chile (33°S), a major city with higher rainfall frequency but where urban pollution plays a significant role.

3.
J Cell Sci ; 113 ( Pt 1): 45-57, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10591624

ABSTRACT

Intercellular junctions have long been considered the main sites through which adherent neutrophils (PMNs) penetrate the endothelium. Tight junctions (TJs; zonula occludens) are the most apical component of the intercellular cleft and they form circumferential belt-like regions of intimate contact between adjacent endothelial cells. Whether PMN transmigration involves disruption of the TJ complex is unknown. We report here that endothelial TJs appear to remain intact during PMN adhesion and transmigration. Human umbilical vein endothelial cell (HUVEC) monolayers, a commonly used model for studying leukocyte trafficking, were cultured in astrocyte-conditioned medium to enhance TJ expression. Immunofluorescence microscopy and immunoblot analysis showed that activated PMN adhesion to resting monolayers or PMN migration across interleukin-1-treated monolayers does not result in widespread proteolytic loss of TJ proteins (ZO-1, ZO-2, and occludin) from endothelial borders. Ultrastructurally, TJs appear intact during and immediately following PMN transendothelial migration. Similarly, transendothelial electrical resistance is unaffected by PMN adhesion and migration. Previously, we showed that TJs are inherently discontinuous at tricellular corners where the borders of three endothelial cells meet and PMNs migrate preferentially at tricellular corners. Collectively, these results suggest that PMN migration at tricellular corners preserves the barrier properties of the endothelium and does not involve widespread disruption of endothelial TJs.


Subject(s)
Cell Movement , Endothelium, Vascular/cytology , Neutrophils/cytology , Tight Junctions/metabolism , Cell Adhesion/drug effects , Cell Movement/drug effects , Cells, Cultured , Culture Media, Conditioned , Electric Conductivity , Endopeptidases/metabolism , Endothelium, Vascular/drug effects , Endothelium, Vascular/metabolism , Endothelium, Vascular/ultrastructure , Freeze Fracturing , Hot Temperature , Humans , Interleukins/pharmacology , Membrane Proteins/chemistry , Membrane Proteins/metabolism , Microscopy, Electron , Microscopy, Fluorescence , Neutrophil Activation/drug effects , Neutrophils/drug effects , Neutrophils/enzymology , Neutrophils/ultrastructure , Occludin , Phosphoproteins/metabolism , Platelet Activating Factor/pharmacology , Tight Junctions/drug effects , Tight Junctions/ultrastructure , Zonula Occludens-1 Protein , Zonula Occludens-2 Protein
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