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1.
Int Nurs Rev ; 66(3): 346-355, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31016729

ABSTRACT

BACKGROUND: Childhood obesity is a complex and multifaceted problem involving interactions among child, family and community environment. AIM: The purpose of this study was to examine the contributing factors to early childhood obesity within a multilevel context, including child and family, childcare setting and community. METHODS: A cross-sectional, quantitative research design was employed. A total of 129 preschoolers and their parents in northwest Florida participated in this study. Child height and weight were measured, and body mass index (BMI) was calculated. Parents and directors of preschools completed survey questionnaires to assess child/family, childcare setting and community factors, respectively. Hierarchical multiple regression was used to evaluate the association of each level of factors with child BMI z-score. RESULTS: Twenty-one per cent of children were overweight or obese (≥85th BMI percentile). In hierarchical multiple regression, household income, parent beliefs, attitudes and practices for child feeding, family obesogenic environment, child routines (screen time on weekends, sleep hours, bedtime) and physical activity environment were significantly related to child BMI z-score. CONCLUSIONS: The findings of this study provide a broader understanding of factors that influence child BMI z-score. Shaping a non-obesogenic environment by establishing healthy routines for children in the home, childcare setting and community is essential in childhood obesity prevention. IMPLICATIONS FOR NURSING PRACTICE AND HEALTH POLICY: Paediatric nurses should routinely assess accurate parental perception of child weight, feeding style and child routines in well-child care visits. Healthcare professionals and health policymakers should enact policies that build a healthy environment for preschoolers in their childcare setting and community.


Subject(s)
Family Relations/psychology , Feeding Behavior/psychology , Parenting/psychology , Pediatric Obesity/prevention & control , Body Mass Index , Child Nutritional Physiological Phenomena , Child, Preschool , Cross-Sectional Studies , Female , Humans , Male , Parents/psychology , Pediatric Obesity/psychology
3.
Am J Transplant ; 15(11): 2837-50, 2015 11.
Article in English | MEDLINE | ID: mdl-26096041

ABSTRACT

Pig islets are an alternative source for islet transplantation to treat type 1 diabetes (T1D), but reproducible curative potential in the pig-to-nonhuman primate (NHP) model has not been demonstrated. Here, we report that pig islet grafts survived and maintained normoglycemia for >6 months in four of five consecutive immunosuppressed NHPs. Pig islets were isolated from designated pathogen-free (DPF) miniature pigs and infused intraportally into streptozotocin-induced diabetic rhesus monkeys under pretreatment with cobra venom factor (CVF), anti-thymocyte globulin (ATG) induction and maintenance with anti-CD154 monoclonal antibody and low-dose sirolimus. Ex vivo expanded autologous regulatory T cells were adoptively transferred in three recipients. Blood glucose levels were promptly normalized in all five monkeys and normoglycemia (90-110 mg/dL) was maintained for >6 months in four cases, the longest currently up to 603 days. Intravenous glucose tolerance tests during the follow-up period showed excellent glucose disposal capacity and porcine C-peptide responses. Adoptive transfer of autologous regulatory T cells was likely to be associated with more stable and durable normoglycemia. Importantly, the recipients showed no serious adverse effects. Taken together, our results confirm the clinical feasibility of pig islet transplantation to treat T1D patients without the need for excessive immunosuppressive therapy.


Subject(s)
Diabetes Mellitus, Type 1/immunology , Diabetes Mellitus, Type 1/surgery , Islets of Langerhans Transplantation/methods , Sirolimus/pharmacology , Transplantation Conditioning/methods , Analysis of Variance , Animals , Biopsy, Needle , Disease Models, Animal , Enzyme-Linked Immunospot Assay , Female , Flow Cytometry , Graft Rejection/immunology , Graft Survival/immunology , Immunocompromised Host , Immunohistochemistry , Islets of Langerhans Transplantation/immunology , Macaca mulatta , Male , Statistics, Nonparametric , Swine , Transplantation, Heterologous
4.
Asian-Australas J Anim Sci ; 27(12): 1721-5, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25358365

ABSTRACT

The objective of this study was to evaluate the in vitro effects of coconut materials on ruminal methanogenesis and fermentation characteristics, in particular their effectiveness for mitigating ruminal methanogenesis. Fistulated Holstein cows were used as the donor of rumen fluid. Coconut materials were added to an in vitro fermentation incubated with rumen fluid-buffer mixture and timothy substrate for 24 h incubation. Total gas production, gas profiles, total volatile fatty acids (tVFAs) and the ruminal methanogens diversity were measured. Although gas profiles in added coconut oil and coconut powder were not significantly different, in vitro ruminal methane production was decreased with the level of reduction between 15% and 19% as compared to control, respectively. Coconut oil and coconut powder also inhibited gas production. The tVFAs concentration was increased by coconut materials, but was not affected significantly as compared to control. Acetate concentration was significantly lower (p<0.05), while propionate was significantly higher (p<0.05) by addition of the coconut materials than that of the control. The acetate:propionate ratio was significantly lowered with addition of coconut oil and coconut powder (p<0.05). The methanogens and ciliate-associated methanogens in all added coconut materials were shown to decrease as compared with control. This study showed that ciliate-associated methanogens diversity was reduced by more than 50% in both coconut oil and coconut powder treatments. In conclusion, these results indicate that coconut powder is a potential agent for decreasing in vitro ruminal methane production and as effective as coconut oil.

5.
Am J Transplant ; 13(6): 1429-40, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23601171

ABSTRACT

Bone marrow-derived early endothelial progenitor cells (BM-EPCs) are a clinical tool for enhancing revascularization. However, the therapeutic efficacy of co-transplantation of BM-EPC with islets has not been investigated. In this study, marginal mass islets were co-transplanted with or without BM-EPCs under the kidney capsules of syngeneic streptozotocin-induced diabetic mice. Using green fluorescent protein transgenic (GFP-Tg) mice as BM-EPC and islet donors or recipients, the role of EPCs in revascularization was assessed for graft morphology, vascular density and fate of EPCs by immunohistochemistry. Islet-EPC co-transplantation improved the outcome of islet transplantation as measured by glucose tolerance, serum insulin level and diabetes reversal rate, compared with transplantation of islets alone. Between groups, the morphology of islet grafts showed significant differences in size and composition of grafted endocrine tissues. Significantly more vessel density derived from donors and recipients was detected with islet-EPC co-transplantation. Abundant GFP-Tg mice-derived BM-EPCs (GFP-EPCs) were observed in or around islet grafts and incorporated into CD31-positive capillaries. Remaining GFP-EPCs expressed VEGF. In conclusion, co-transplantation of islets with BM-EPCs could improve the outcome of marginal mass islet transplantation by promoting revascularization and preserving islet morphology.


Subject(s)
Bone Marrow Cells/cytology , Endothelium, Vascular/cytology , Graft Survival/physiology , Islets of Langerhans Transplantation , Islets of Langerhans/blood supply , Stem Cell Transplantation/methods , Stem Cells/cytology , Animals , Disease Models, Animal , Endothelial Cells , Male , Mice , Mice, Inbred C57BL
6.
AIDS Care ; 25(4): 488-95, 2013.
Article in English | MEDLINE | ID: mdl-22909386

ABSTRACT

Identifying both Human immunodeficiency virus (HIV)-related and co-morbid symptoms experienced by people living with HIV (PLWH) who are receiving antiretroviral therapy (ART) treatment is a major challenge for healthcare providers globally. Yet, little research to date has examined the symptoms of illness experienced by PLWH including patients living in Central and South American. To address this gap, this study was designed to identify symptoms of HIV by socio-demographic and/or clinical characteristics among Chilean patients living with the virus. A convenience sample of 209 Chilean PLWH was recruited from an outpatient clinic in Santiago, Chile. A structured interview was used to elicit socio-demographic information and HIV symptoms status. Additional clinical information was obtained through a review of the participants' medical records. Results show that patients' most commonly reported HIV-related symptoms were fear/worries (66%), anxiety (52%), gas/bloating (50%), and thirst (50%). Multivariate analysis revealed a positive association between the number of reported HIV-related symptoms and number of years living with HIV. Having completed college was negatively associated with number of symptoms. Latent class analysis indicated that PLWH in the sample who had completed college were two times more likely to experience a mild intensity of HIV-related symptoms than their lesser educated counterparts. Similarly, logistic regression revealed that college-educated PLWH were twice as likely to be classified in the subgroup reporting mild intensity of symptoms than those who lacked a college degree. Overall, the study's results reveal that many Chilean PLWH, even those with high CD4 counts and low or undetectable viral loads, are not symptom free. The findings point to the need for clinicians to tailor a plan of care for individuals living with HIV that is based on their symptomatology.


Subject(s)
Anxiety/epidemiology , HIV Infections/epidemiology , Adolescent , Adult , Aged , Anxiety/etiology , CD4 Lymphocyte Count , Chile/epidemiology , Cluster Analysis , Comorbidity , Cross-Sectional Studies , Female , HIV Infections/complications , Humans , Male , Middle Aged , Surveys and Questionnaires , Thirst , Time Factors , Viral Load
7.
Horm Metab Res ; 43(9): 642-5, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21823060

ABSTRACT

Metabolic syndrome is a complex clinical disorder characterized by obesity, a disturbance of glucose metabolism, dyslipidemia, and hypertension, leading to increased cardiovascular risk. Macrophage migration inhibitory factor (MIF) is a proinflammatory cytokine produced both by innate immune cells and by adipocytes, and it plays an important role in inflammatory and cardiovascular diseases. The goal of this study was to evaluate the expression of circulating MIF in patients with metabolic syndrome. A study was conducted involving 172 persons who attended the Jeju National University Hospital Health Promotion Center. Among the 172 subjects, 88 patients with metabolic syndrome and 84 healthy control subjects were included. Serum MIF levels were considerably higher in patients with metabolic syndrome than in healthy subjects (mean±SEM, 1413.0-pg/ml±102.6 vs. 1077.0-pg/ml±-91.3, p=0.016). Among the metabolic syndrome patients, MIF levels were significantly increased in women (1403.0-pg/ml±114.2 vs. 921.3 pg/ml±117.3, p=0.005), but not in men. Even after further linear regression adjustment for age and body mass index, the expression of MIF for women with metabolic syndrome was still clearly elevated when compared to healthy subjects (p=0.011). Circulating MIF concentrations showed a gender disparity between healthy and metabolic syndrome subjects. An elevation of systemic MIF in women with metabolic syndrome may contribute to pathogenesis of metabolic syndrome or to the development of metabolic syndrome-related diseases, such as atherosclerosis and type 2 diabetes mellitus.


Subject(s)
Macrophage Migration-Inhibitory Factors/blood , Metabolic Syndrome/blood , Adult , Case-Control Studies , Cross-Sectional Studies , Female , Humans , Male , Middle Aged , Sex Factors
8.
J Med Primatol ; 40(3): 188-93, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21332756

ABSTRACT

BACKGROUND: A newly acquired rhesus macaque was suffering from rapid destruction of the left cheek caused by necrotizing stomatitis. METHODS: To restore reconstructive surgery and intensive care with antibiotics, wound protection, wound healing agents, and debridement were applied. RESULTS: Staphylococcus aureus and Enterococcus faecalis were isolated from the culture of the lesion, and the antibiotic susceptibility test revealed methicillin-resistant Staphylococcus aureus infection. Vancomycin and ampicillin-sulbactam effectively treated the bacterial infections, and reconstructive surgery was performed once the infection was cleared. Topical application of recombinant human epidermal growth factor (rhEGF) was useful to treat exposed wound of the noma lesion. CONCLUSIONS: Simian noma associated with methicillin-resistant Staphylococcus aureus (MRSA) had not previously been reported in non-human primates. Although noma associated with MRSA is hard to cure because of its rapid and destructive progress, the aggressive therapy used in this study led to the successful resolution of an acute necrotic stomatitis lesion in a rhesus macaque.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Enterococcus faecalis/isolation & purification , Gram-Positive Bacterial Infections/microbiology , Macaca mulatta , Methicillin-Resistant Staphylococcus aureus/isolation & purification , Monkey Diseases/microbiology , Noma/veterinary , Staphylococcal Infections/veterinary , Ampicillin/therapeutic use , Animals , Enterococcus faecalis/classification , Enterococcus faecalis/drug effects , Epidermal Growth Factor/therapeutic use , Gram-Positive Bacterial Infections/drug therapy , Gram-Positive Bacterial Infections/surgery , Humans , Male , Methicillin-Resistant Staphylococcus aureus/classification , Methicillin-Resistant Staphylococcus aureus/drug effects , Monkey Diseases/drug therapy , Monkey Diseases/surgery , Mouth/pathology , Mouth/surgery , Necrosis/drug therapy , Necrosis/microbiology , Necrosis/surgery , Necrosis/veterinary , Noma/drug therapy , Noma/microbiology , Noma/surgery , Oral Surgical Procedures/veterinary , Plastic Surgery Procedures/veterinary , Staphylococcal Infections/drug therapy , Staphylococcal Infections/microbiology , Staphylococcal Infections/surgery , Stomatitis/drug therapy , Stomatitis/microbiology , Stomatitis/surgery , Stomatitis/veterinary , Sulbactam/therapeutic use , Vancomycin/therapeutic use , Wound Healing
9.
J Exp Med ; 183(2): 669-74, 1996 Feb 01.
Article in English | MEDLINE | ID: mdl-8627180

ABSTRACT

CD30 is a member of the tumor necrosis factor superfamily and a surface marker for Hodgkin's disease. Normal activated T cells and several virally transformed T or B cell lines also show CD30 expression. The interaction of CD30 with its ligand induces cell death or proliferation, depending on the cell type. In this report we characterize the signals mediated by the intracellular domain of CD30 and show that, in combination with signal(s) transduced by the T cell receptor, the multimerization of CD30 cytoplasmic domain induces Fas(CD95)-independent cell death in T cell hybridomas. Deletion analysis shows that the COOH-terminal 66 amino acids of CD30 are required to induce cell death. Using the yeast two-hybrid system, we have identified that the same region of CD30 interacts with tumor necrosis factor receptor-associated factor (TRAF)1 and TRAF2. These results indicate that TRAF1 and/or TRAF2 play an important role in cell death in addition to their previously identified roles in cell proliferation.


Subject(s)
Cell Death/physiology , Ki-1 Antigen/metabolism , Receptors, Antigen, T-Cell/metabolism , Signal Transduction , T-Lymphocytes/physiology , Base Sequence , Hybridomas/physiology , Ki-1 Antigen/genetics , Molecular Sequence Data , Protein Binding , Proteins/metabolism , Receptors, Tumor Necrosis Factor/metabolism , Recombinant Fusion Proteins , Structure-Activity Relationship , TNF Receptor-Associated Factor 1 , TNF Receptor-Associated Factor 2 , Transfection
10.
J Exp Med ; 178(2): 737-41, 1993 Aug 01.
Article in English | MEDLINE | ID: mdl-7688034

ABSTRACT

It has recently been shown that open reading frames in the 3' long terminal repeats of mouse mammary tumor viruses encode superantigens. These viral superantigens (vSAGs) stimulate most T cells expressing appropriate V beta s almost regardless of the rest of the variable components of the T cell receptors (TCR) expressed by those cells. vSAGs produce a type II integral membrane protein with a nonessential short cytoplasmic domain and a large glycosylated extracellular COOH-terminal domain, which is predicted to interact with major histocompatibility complex class II molecules and the TCR. The transmembrane region of vSAG also has an internal positively charged lysine residue of unknown significance. A set of chimeric and mutant vSAG genes has been used in transfection experiments to show that only the extreme COOH-terminal portion of vSAGs determine their TCR V beta specificities, and to show that the lysine residue in the transmembrane domain is not essential for the function of vSAG.


Subject(s)
Antigens, Viral/immunology , Mammary Tumor Virus, Mouse/immunology , Receptors, Antigen, T-Cell, alpha-beta/immunology , Amino Acid Sequence , Antigens, Viral/chemistry , Antigens, Viral/genetics , Base Sequence , Carboxylic Acids/chemistry , Cell Membrane , DNA, Single-Stranded , Electrochemistry , Epitopes/chemistry , Histocompatibility Antigens Class II/immunology , Lysine/chemistry , Lysine/immunology , Mammary Tumor Virus, Mouse/genetics , Molecular Sequence Data , Mutation , Tumor Cells, Cultured
11.
J Exp Med ; 181(5): 1899-904, 1995 May 01.
Article in English | MEDLINE | ID: mdl-7722465

ABSTRACT

The mouse mammary tumor virus-7 superantigen (vSAG7) is proteolytically processed in B cells at as many as three positions. Proteolytic processing appears to be important for superantigen activity because a processed form of vSAG7 was predominant among those forms that were found to bind to major histocompatibility complex class II molecules. To determine the functional significance of proteolytic processing, a mutation was introduced in vSAG7 at one of the sites where proteolytic cleavage is thought to take place in B cells. Elimination of the putative processing site at position 171 abrogated detectable vSAG7 surface expression in B cells, indicating that proteolytic processing is required for vSAG7 function. Coexpression in insect cells of vSAG7 and furin, a proprotein-processing enzyme, also demonstrated that furin could process vSAG7 at position 171.


Subject(s)
Antigen Presentation , Antigens, Viral/metabolism , Gammaretrovirus/immunology , Superantigens/metabolism , Amino Acid Sequence , Animals , Base Sequence , Furin , Molecular Sequence Data , Spodoptera , Subtilisins/metabolism , Tumor Cells, Cultured
12.
Int J Clin Pharmacol Ther ; 48(8): 497-503, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20650039

ABSTRACT

OBJECTIVES: To explore if non-concurrent amlodipine dosing results in less drug interaction, the pharmacokinetic profiles, safety and efficacy endpoints were assessed following repeated doses of simvastatin, co-administered concurrently or non-concurrently with amlodipine in patients with coexisting hypertension and hyperlipidemia. METHODS: Seventeen patients randomly received daily doses of 20 mg simvastatin and 5 mg amlodipine for 6 weeks, either with both drugs at 7:00 PM (concurrent) or with simvastatin at 7:00 PM followed by amlodipine at 11:00 PM (non-concurrent). The maximum plasma concentration (Cmax) and the area under the concentration-time curve up to the last quantifiable concentration (AUClast) were estimated at steady state. Lipid profiles and blood pressure values were also compared between the concurrent and non-concurrent groups. RESULTS: The Cmax and AUClast and of simvastatin acid in the non-concurrent amlodipine dosing group were 63.2% and 66.0%, respectively, of the values obtained in the concurrent group (1.2 +/- 1.0 vs. 1.9 +/- 0.9 ng/ml and 10.3 +/- 8.3 vs. 15.6 +/- 7.5 h ng/ml, respectively, mean +/- standard deviation). Changes from baseline in lipid profile and blood pressure were comparable between the groups. CONCLUSIONS: Non-concurrent dosing may be a useful and safe therapeutic option for patients who require two or more drugs administered concomitantly, but who are likely to develop unwanted drug interactions.


Subject(s)
Amlodipine/pharmacology , Antihypertensive Agents/pharmacology , Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacokinetics , Simvastatin/pharmacokinetics , Adult , Aged , Amlodipine/administration & dosage , Antihypertensive Agents/administration & dosage , Area Under Curve , Drug Administration Schedule , Drug Interactions , Female , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/administration & dosage , Hyperlipidemias/complications , Hyperlipidemias/drug therapy , Hypertension/complications , Hypertension/drug therapy , Male , Middle Aged , Simvastatin/administration & dosage
13.
Environ Technol ; 31(1): 15-27, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20232675

ABSTRACT

The major objective of this study was to delineate the oxidation of diethyl phthalate (DEP) in water, using bench-scale UV/H2O2 and O3/H2O2 processes, and to determine the effects of nitrate (NO(3-)-N, 5 mg L(-1)) on this oxidation. The oxidation of DEP was also investigated through a pilot-scale advanced oxidation process (AOP), into which a portion of the effluent from a pilot-scale membrane bioreactor (MBR) plant was pumped. The bench-scale operation showed that DEP could be oxidized via solely UV oxidation or O3 oxidation. The adverse effect of nitrate on the DEP oxidation was remarkable in the UV/H2O2 process, and the nitrate clearly reduced its oxidation. The adverse effect of nitrate on O3 oxidation was also observed. It was noted, however, that the nitrate clearly enhanced the DEP oxidation in the O3/H2O2 process. A series of pilot-scale AOP operations indicated that the addition of H2O2 enhanced DEP oxidation in both the UV/H2O2 and O3/H2O2 processes. No noticeable adverse effect of nitrate was observed in the NO(3-)-N concentration of about 6.0 mg L(-1), which was naturally contained in the treatment stream. About 52% and 61% of the DEP were oxidized by each of these two oxidation processes in this pilot-scale operation. Both the UV/H2O2 and O3/H2O2 processes appeared to be desirable alternatives for DEP oxidation in treatment effluent streams.


Subject(s)
Hydrogen Peroxide/chemistry , Nitrates/chemistry , Oxygen/chemistry , Ozone/chemistry , Phthalic Acids/chemistry , Water Pollutants, Chemical/chemistry , Water Purification/methods , Hydrogen Peroxide/radiation effects , Nitrates/radiation effects , Oxidation-Reduction , Oxygen/radiation effects , Ozone/radiation effects , Phthalic Acids/isolation & purification , Phthalic Acids/radiation effects , Pilot Projects , Ultraviolet Rays , Water Pollutants, Chemical/isolation & purification , Water Pollutants, Chemical/radiation effects
14.
Science ; 200(4343): 727-30, 1978 May 19.
Article in English | MEDLINE | ID: mdl-17743223

ABSTRACT

Radiation from electrical power lines leaks into the magnetosphere and stimulates strong very-low-frequency wave activity out to many earth radii. Observations in Antarctica show that wave activity induced by power lines tends to occur during the daytime when power consumption is high in the source region in eastern Canada. The wave frequency ranges from 1 to 8 kilohertz. This man-made wave activity may have significant effects on energetic electrons trapped in the earth's radiation belts.

15.
Int J Immunogenet ; 36(1): 59-64, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19207937

ABSTRACT

Small ubiquitin-like modifiers (SUMOs) are structurally related to ubiquitin and are ligated to lysine residues within sumoylation target proteins. Currently, a growing body of evidence shows that the SUMO family has evolved as an important modifier of many proteins in a variety of cellular pathways. In this study, we have cloned cDNA encoding for three different pig SUMO isoforms. The full-length cDNA encoding for pig Sumo1, Sumo2 and Sumo4 consists of 306, 288 and 288 nucleotide base pairs of the open reading frame, respectively, and the putative amino acid sequences of pig Sumo1, Sumo2 and Sumo4 are composed of 101, 95 and 95 peptides, respectively. The structures of pig SUMOs are evolutionally well conserved, and their expression has been detected in a broad range of tissues. We also determined that all pig SUMOs are localized within the nucleus. However, the different tissue expression observed in individual pig SUMOs may show the divergent or specialized role of each of the pig SUMO isoforms. Future studies will focus on the identification of targets for sumoylation by different pig SUMO isoforms and the analysis of the functional consequences of sumoylation during the course of infectious diseases in pigs.


Subject(s)
Cell Nucleus/metabolism , Small Ubiquitin-Related Modifier Proteins/biosynthesis , Sus scrofa/metabolism , Amino Acid Sequence , Animals , Base Sequence , CHO Cells , Cloning, Molecular , Cricetinae , Cricetulus , Gene Expression , Molecular Sequence Data , Phylogeny , Protein Isoforms/genetics , Protein Isoforms/metabolism , Sequence Alignment , Small Ubiquitin-Related Modifier Proteins/genetics , Sus scrofa/genetics
16.
Oncogene ; 38(25): 5108-5110, 2019 Jun.
Article in English | MEDLINE | ID: mdl-30926886

ABSTRACT

The original version of this article contained an error in the published figures Fig 2 and Fig 3f, where the information was inadvertently duplicated. This error does not alter the conclusions of the paper. The corrected figures are published in this correction notice. The authors sincerely apologize for this error.

17.
Oncogene ; 38(20): 3970-3971, 2019 May.
Article in English | MEDLINE | ID: mdl-30679788

ABSTRACT

Following the publication of this article the authors noted that images were inadvertently duplicated in Fig. 1b. The corrected Fig. 1 can be found in the associated Correction. The conclusions of this paper are not affected. The authors sincerely apologize for this error. This error has not been corrected in the HTML or PDF of the original Article.

18.
Int J Clin Pract ; 62(9): 1306-12, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18643931

ABSTRACT

A consensus meeting of leading Asian hypertension experts was held in January 2007 in Seoul, Korea, to discuss how to address the growing challenge of hypertension management in the region. This report summarises key recommendations from the group, including: raising public awareness about the impact of hypertension; improving physician education and training; increasing early detection, for example through routine blood pressure measurement; and development and adoption of pan-Asian treatment guidelines, which would greatly facilitate research into hypertension and its management. The group conclude that these challenges can only be met through a collaborative effort of government, healthcare professionals, food and healthcare industries, and patients and the public. Food and healthcare industries need to develop healthy foods and support healthy living programmes, while increasing research into antihypertensive medications in Asia. Government officials and policy makers need to be made aware of the value of investing in hypertension awareness, prevention and management programmes.


Subject(s)
Hypertension/therapy , Adult , Asia , Clinical Competence/standards , Early Diagnosis , Education, Medical/standards , Health Personnel/education , Health Personnel/standards , Health Services Accessibility , Humans , Hypertension/mortality , Hypertension/prevention & control , Middle Aged , Patient Compliance , Patient Education as Topic/standards , Practice Guidelines as Topic , Prevalence , Socioeconomic Factors
19.
Water Sci Technol ; 58(5): 1031-7, 2008.
Article in English | MEDLINE | ID: mdl-18824801

ABSTRACT

One of the objectives of this study was to delineate the effect of nitrate on diethyl phthalate (DEP) oxidation by conducting a bench-scale ultraviolet (UV)/H2O2 and O3/H2O2 operations as suggested in a previous study. We also aim to investigate DEP oxidation at various UV doses and H2O2 concentrations by performing a pilot-scale advanced oxidation processes (AOP) system, into which a portion of the effluent from a pilot-scale membrane bioreactor (MBR) plant was pumped. In the bench-scale AOP operation, the O3 oxidation alone as well as the UV irradiation without H2O2 addition could be among the desirable alternatives for the efficient removal of DEP dissolved in aqueous solutions at a low DEP concentration range of 85+/-15 microg/L. The adverse effect in the UV/H2O2 process was significantly greater than that in the UV oxidation alone, and its oxidation was almost halved by the nitrate. However, the nitrate clearly enhanced the DEP oxidation in the O3 oxidation and O3/H2O2 process. Especially, the addition of nitrate almost doubled the DEP oxidation efficiency in the O3/H2O2 process. The series of pilot-scale AOP operations confirmed that about 30-50% of DEP dissolved in the treated MBR effluent streams was, at least, oxidized by the O3 oxidation alone as well as the UV irradiation without H2O2 addition. The UV photolysis of H2O2 was most effective for DEP degradation with an H2O2 concentration of 40 mg/L at a UV dose of 500 mJ/cm2.


Subject(s)
Hydrogen Peroxide/chemistry , Nitrates/chemistry , Phthalic Acids/chemistry , Bioreactors , Oxidation-Reduction/radiation effects , Ultraviolet Rays , Water Purification/instrumentation , Water Purification/methods
20.
J Hum Hypertens ; 21(2): 141-8, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17136108

ABSTRACT

Blood pressure (BP) is one of the most important contributing factors to pulse wave velocity (PWV), a classic measure of arterial stiffness. Although there have been many non-invasive studies to show the relation between arterial stiffness and BP, the results are controversial. The aim of this study is to evaluate the role of BP as an influencing factor on PWV using invasive method. We observed 174 normotensive and untreated hypertensive subjects using coronary angiography. Arterial stiffness was assessed through aorto-femoral PWV by foot-to-foot velocity method using fluid-filled system. And BP was measured by pressure wave at the right common femoral artery. From univariate analysis, age, diabetes mellitus (DM), hypertension, waist, waist-to-hip ratio, total cholesterol-to-high-density lipoprotein cholesterol ratio, systolic BP (SBP), pulse pressure (PP) and mean arterial pressure (MAP) showed significant association with PWV. To avoid multiple colinearity among SBP, PP and MAP, we performed multiple regression analysis predicting PWV thrice. Age, DM and each BP were significantly and consistently correlated to PWV. In the first and third modules, compared to age, SBP and MAP were less strong predictors, respectively. However, PP was the stronger predictor than age and DM in the second module. Lastly, we simultaneously forced MAP and PP with other variables in the fourth multivariate analysis. Age, DM and PP remained significantly correlated with PWV, but the significance of MAP was lost. This is the first invasive study to suggest that PP has the strongest correlation with PWV among a variety of BP parameters.


Subject(s)
Blood Flow Velocity/physiology , Blood Pressure , Hypertension/physiopathology , Pulsatile Flow/physiology , Adult , Age Factors , Aged , Cholesterol, HDL/blood , Diabetes Mellitus/physiopathology , Elasticity , Female , Heart Rate , Humans , Male , Middle Aged , Sex Characteristics
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