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1.
Environ Monit Assess ; 186(8): 4697-708, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24729178

ABSTRACT

Decline of pedunculate oak (Quercus robur L.) was studied in SW Finland. This is a region where the species is growing near its northern distributional limit globally and a recent decline of mature trees has been described regionally. Tree rings of declining oaks were compared to the chronologies of healthy and oaks that died, climate series and stable isotope discrimination of carbon (δ(13)C) of comparable mature trees. The radial growth (earlywood, latewood, and annual ring width) of declining oaks was clearly deteriorated in comparison to healthy oaks, but recuperated, compared to oaks that died, through all index types. Comparison of climate relationships between growth and δ(13)C, expected to reflect oaks' intrinsic water use efficiency, indicated enhancing resistance to droughts through the growing season. The growth and the climatic growth response was differentiated in declining oaks as compared with the healthy and oaks that died revealing that: (1) declining oaks exhibited decreasing competitive strength as indicated by reduced overall growth relative to healthy oaks, (2) the growth of declining oaks was more sensitive to winter conditions, but less restricted by summer droughts than the growth of other oaks, and (3) healthy oaks were seen having benefitted from the ongoing lengthening of the growing season. Lack of correlativity between growth and δ(13)C became evident as their responses to temperature and precipitation variations deviated drastically during the other but summer months. Our results indicate that several different ecological factors, rather than a single climatic factor (e.g., drought), are controlling the oak decline in the studied environment.


Subject(s)
Climate , Environmental Monitoring/methods , Quercus/growth & development , Carbon Isotopes/analysis , Climate Change , Droughts , Environment , Finland , Seasons , Temperature
2.
Phys Rev Lett ; 99(19): 190408, 2007 Nov 09.
Article in English | MEDLINE | ID: mdl-18233055

ABSTRACT

We present a simple but efficient geometrical method for determining the inert states of spin-S systems. It can be used if the system is described by a spin vector of a spin-S particle and its energy is invariant in spin rotations and phase changes. Our method is applicable to an arbitrary S and it is based on the representation of a pure spin state of a spin-S particle in terms of 2S points on the surface of a sphere. We use this method to find candidates for some of the ground states of spinor Bose-Einstein condensates.

3.
Cochrane Database Syst Rev ; (4): CD004977, 2004 Oct 18.
Article in English | MEDLINE | ID: mdl-15495133

ABSTRACT

BACKGROUND: Pneumonia, most commonly caused by Streptococcus pneumoniae (Pnc), is a major cause of morbidity and mortality among young children especially in developing countries. Recently, the prevalence of antibiotic-resistant Pnc has increased worldwide such that the effectiveness of preventive strategies, like the new pneumococcal conjugate vaccines (PCV) on rates of invasive pneumococcal disease (IPD) and pneumonia, needs to be evaluated. OBJECTIVES: To determine the efficacy of PCV in reducing the incidence of IPD due to vaccine serotypes (VT) and x-ray confirmed pneumonia with consolidation of unspecified etiology in children who received PCV before 12 months of age. SEARCH STRATEGY: We searched the following databases: the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library, Issue 1 2004), MEDLINE (1990 to March 2004) and EMBASE (1990 to December 2003). Reference list of articles, and books of abstracts of relevant symposia, were hand searched. Researchers in the field were also contacted. SELECTION CRITERIA: Randomised controlled trials (RCTs) comparing PCV with placebo, or another vaccine, among children below two years with IPD and clinical/radiographic pneumonia as outcomes. DATA COLLECTION AND ANALYSIS: Two reviewers independently identified eligible studies, assessed trial quality, and extracted data. Differences were resolved by discussion. The inverse variance method was used to pool effect sizes. MAIN RESULTS: We identified four trials assessing the efficacy of PCV in reducing the incidence of IPD, two on x-ray confirmed pneumonia as outcome, and one on clinical pneumonia, with or without x-ray confirmation. Results from pooling HIV-1 negative children from the South African study with the other studies were as follows: the pooled vaccine efficacy (VE) for vaccine-type IPD was 88% (95% confidence interval (CI) 73% to 94%; fixed effect and random effects models), the effect measure was statistically significant (p <0.00001) and there was no heterogeneity (p = 0.77I2 0%); the pooled VE for all-serotype IPD was 66% (95% CI 46% to 79%; fixed effect model), the effect measure was statistically significant (p <0.00001) and there was no statistical heterogeneity (p = 0.09, I2 51%); the pooled VE for x-ray confirmed pneumonia was 22% (95% CI 11% to 31%; both fixed effect and random effects models) and there was no statistical heterogeneity (p = 0.80, I2 0%). Analyses that included all the children in the South African study (HIV-1 negative and HIV-1 positive children) and pooled with data from the other studies gave very similar results. REVIEWERS' CONCLUSIONS: PCV is effective in reducing the incidence of IPD from all serotypes but exerts a greater effect in reducing VT IPD. Although PCV is also effective in reducing the incidence of x-ray confirmed pneumonia, there are still uncertainties about the definition of this outcome. Additional randomised controlled trials are currently in progress.


Subject(s)
Pneumococcal Infections/prevention & control , Pneumococcal Vaccines/therapeutic use , Humans , Infant , Pneumonia, Pneumococcal/diagnostic imaging , Pneumonia, Pneumococcal/prevention & control , Radiography , Vaccines, Conjugate/therapeutic use
4.
J Med Genet ; 40(10): 741-6, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14569119

ABSTRACT

BACKGROUND: The Schmid type of metaphyseal chondrodysplasia (MCDS) is generally due to mutations in COL10A1 encoding for type X collagen of cartilage. METHODS: We performed a study on the genes coding for the RNA components of RNase MRP (MRPR) and RNase P (H1RNA) among 20 patients with diagnosis of MCDS and no mutations in COL10A1. RESULTS: Two patients were found to be homozygous for a base substitution G for A at nucleotide 70 of RMRP, which is the major mutation causing cartilage-hair hypoplasia. No pathogenic mutations were detected in H1RNA. CONCLUSION: Cartilage-hair hypoplasia diagnosis should be considered in patients with metaphyseal chondrodysplasia even in the absence of any extra-skeletal manifestations if no mutation in COL10A1 can be found and the family history is compatible with autosomal recessive inheritance. Correct diagnosis is important for genetic counselling and for proper follow up of the patients.


Subject(s)
Endoribonucleases/genetics , Mutation , Osteochondrodysplasias/genetics , RNA, Catalytic/genetics , Child, Preschool , Humans , Male , Osteochondrodysplasias/diagnosis , Osteochondrodysplasias/diagnostic imaging , RNA/genetics , Radiography , Ribonuclease P
5.
Biochem Biophys Res Commun ; 289(4): 813-8, 2001 Dec 14.
Article in English | MEDLINE | ID: mdl-11735118

ABSTRACT

T1 relaxation in the rotating frame (T1rho) is a sensitive magnetic resonance imaging (MRI) contrast for acute brain insults. Biophysical mechanisms affecting T1rho relaxation rate (R1rho) and R1rho dispersion (dependency of R1rho on the spin-lock field) were studied in protein solutions by varying their chemical environment and pH in native, heat-denatured, and glutaraldehyde (GA) cross-linked samples. Low pH strongly reduced R1rho in heat-denatured phantoms displaying proton resonances from a number of side-chain chemical groups in high-resolution 1H NMR spectra. At pH of 5.5, R1rho dispersion was completely absent. In contrast, in the GA-treated phantoms with very few NMR visible side chain groups, acidic pH showed virtually no effect on R1rho. The present data point to a crucial role of proton exchange on R1rho and R1rho dispersion in immobilized protein solution mimicking tissue relaxation properties.


Subject(s)
Magnetic Resonance Spectroscopy/methods , Proteins/chemistry , Animals , Biophysical Phenomena , Biophysics , Brain Ischemia/metabolism , Cattle , Cross-Linking Reagents , Glutaral , Hydrogen-Ion Concentration , In Vitro Techniques , Magnetic Resonance Imaging , Phantoms, Imaging , Protein Denaturation , Protons , Serum Albumin, Bovine/chemistry , Solutions
6.
J Cereb Blood Flow Metab ; 20(10): 1457-66, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11043908

ABSTRACT

The impact of brain imaging on the assessment of tissue status is likely to increase with the advent of treatment methods for acute cerebral ischemia. Multimodal magnetic resonance imaging (MRI) demonstrates potential for selecting stroke therapy patients by identifying the presence of acute ischemia, delineating the perfusion defect, and excluding hemorrhage. Yet, the identification of tissue subject to reversible or irreversible ischemia has proven to be difficult. Here, the authors show that T1 relaxation time in the rotating frame, so-called T1rho, serves as a sensitive MRI indicator of cerebral ischemia in the rat. The T1rho prolongs within minutes after a drop in the CBF of less than 22 mL 100 g(-1) min(-1). Dependence of T1rho on spin-lock amplitude, termed as T1rho dispersion, increases by approximately 20% on middle cerebral artery (MCA) occlusion, comparable with the magnitude of diffusion reduction. The T1rho dispersion change dynamically increases to be 38% +/- 10% by the first 60 minutes of ischemia in the brain region destined to develop infarction. Following reperfusion after 45 minutes of MCA occlusion, the tissue with elevated T1rho dispersion (yet normal diffusion) develops severe histologically verified neuronal damage; thus, the former parameter unveils an irreversible condition earlier than currently available MRI methods. The T1rho dispersion as a novel MRI index of cerebral ischemia may be useful in determination of the therapeutic window for acute ischemic stroke.


Subject(s)
Brain Ischemia/diagnosis , Magnetic Resonance Imaging/methods , Animals , Arterial Occlusive Diseases/diagnosis , Arterial Occlusive Diseases/pathology , Arterial Occlusive Diseases/physiopathology , Body Temperature , Brain/physiopathology , Brain Ischemia/physiopathology , Cerebral Arteries , Cerebrovascular Circulation , Male , Nerve Tissue Proteins/metabolism , Phantoms, Imaging , Rats , Rats, Wistar , Time Factors
7.
Int Psychogeriatr ; 12(4): 473-81, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11263714

ABSTRACT

BACKGROUND: The etiologic factors of delirium have been frequently studied in hospitalized elderly patients who usually have an underlying disorder, i.e., hip fracture or dementia predisposing to delirium. The etiologic factors of delirium and prognosis in healthy elderly remain unstudied. The aim of our study was to detect the primary and additional etiologic factors contributing to delirium among community-dwelling healthy elderly people without predisposing disorders to delirium and to evaluate 1-year prognosis after discharge to home. METHOD: The study subjects consisted of 51 community-dwelling people over 65 years of age, without severe underlying disorders predisposing to delirium, admitted consecutively to the hospital because of a delirious state. The diagnosis of delirium was based on the DSM-III-R criteria. After discharge to home, the subjects were followed up for 1 year. RESULTS: The most important primary causes of delirium were infections in 22 cases (43%) and cerebrovascular attacks in 13 cases (25%). After the 1-year follow-up period, 10 patients (20%) had been taken into long-term care and 5 patients (10%) had died. DISCUSSION: The plausible etiologic factor of delirium was detected in all cases. Among healthy elderly people, infections and cerebrovascular attacks were the most important etiologic factors for delirium. After discharge to home, 30% of the patients had to be taken into long-term care or had died within 1 year of the delirium.


Subject(s)
Cerebrovascular Disorders/complications , Delirium/etiology , Infections/complications , Acute Disease , Aged , Aged, 80 and over , Cause of Death , Delirium/diagnosis , Delirium/mortality , Diagnosis, Differential , Female , Finland/epidemiology , Follow-Up Studies , Humans , Institutionalization/statistics & numerical data , Male , Survival Analysis
8.
Int J Surg Investig ; 2(1): 33-9, 2000.
Article in English | MEDLINE | ID: mdl-12774336

ABSTRACT

BACKGROUND: Laparoscopic operation has replaced conventional operation in the treatment of reflux disease. This change has been mostly based on excellent results from highly experienced antireflux surgeons rather than on randomized clinical trials. AIMS: The objective of this study was to compare the short-term symptomatic outcome and patient quality of life costs after laparoscopic (LNF) or open Nissen fundoplication (ONF) in a community hospital setting with less experienced surgeons. METHODS: Forty-two patients with documented gastroesophageal reflux disease (GERD) were randomized to either LNF or ONF. Symptomatic outcome using a custom questionnaire and the Gastrointestinal Quality of Life Index (GIQLI) were measured pre- and postoperatively at one and three months. RESULTS: Esophagitis was cured among all patients in LNF group compared to 90% in the ONF group. The symptoms observed preoperatively were significantly improved in both groups, except for dysphagia and flatulence. Dysphagia was more common after LNF. The GIQLI (scale 0-144) was equally normalized in both groups. The mean GIQLI-change among all patients was 37.9 points. Patient satisfaction did not differ between the groups. CONCLUSIONS: LNF and ONF are effective methods in the operative treatment of GERD in short-term and result in a significant improvement in patients gastrointestinal symptoms and quality of life.


Subject(s)
Fundoplication/methods , Gastroesophageal Reflux/surgery , Laparoscopy , Quality of Life , Adult , Aged , Female , Gastroesophageal Reflux/diagnosis , Humans , Male , Middle Aged , Prospective Studies , Treatment Outcome
9.
J Am Coll Surg ; 188(4): 368-76, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10195720

ABSTRACT

BACKGROUND: Laparoscopic antireflux surgery has replaced conventional operation despite the fact that currently no randomized trials have been published regarding its cost effectiveness. The objective of the present study was to compare costs and some short-term outcomes of laparoscopic and open Nissen fundoplication. STUDY DESIGN: Forty-two patients with documented gastroesophageal reflux disease were randomized between October 1995 and October 1996 to either laparoscopic (LNF) or open (ONF) Nissen fundoplication. Some short-term outcomes, Gastrointestinal Quality of Life Index (GIQLI) hospital costs, and costs to society were assessed. Followup was 3 months. RESULTS: Medians of operation times in the LNF and ONF groups were 98 min and 74 min, respectively. Hospital stay was 2.5 days shorter after laparoscopic operation (LNF 3 days versus ONF 5.5 days). Both operations were equally safe and effective, but the LNF group experienced significantly less pain and fatigue during the first 3 postoperative weeks. Improvement in the GIQLI and overall patient satisfaction were comparable between the methods. Convalescence was faster in the LNF group: return to normal life being 14 versus 31 days and return to work being 21 versus 44 days in the LNF and ONF groups, respectively. Hospital costs were similar, $2,981 and $3,140 in the LNF and ONF groups, respectively, but total costs were lower ($7,506 versus $13,118) in the LNF group as a result of an earlier return to work. CONCLUSIONS: LNF is superior in cost effectiveness, assuming that the longterm results between the methods are comparable.


Subject(s)
Fundoplication/economics , Fundoplication/methods , Gastroesophageal Reflux/economics , Gastroesophageal Reflux/surgery , Laparoscopy/economics , Costs and Cost Analysis , Follow-Up Studies , Humans , Prospective Studies
11.
Leuk Lymphoma ; 2(1-2): 127-9, 1990.
Article in English | MEDLINE | ID: mdl-27456579

ABSTRACT

The actual use of hospital beds for patients with multiple myeloma was calculated from a randomised trial of primary treatment with either melphalan and prednisone (MP, 66 patients) or intensive combination chemotherapy with vincristine, cyclophosphamide, lomustine, melphalan and methylprednisolone (MOCCA, 64 patients). The survival of the patients was similar in both arms, and the samples, 20 and 32 patients, respectively, were well representative for the whole arms. The average numbers of hospital days were similar fur both arms. For the first year MP 33.2 (SD 27.6) vs. MOCCA 32.1 (SD 19.0), and during the first to 4th years 78.5 (SD 45.9) vs. 67.8 (SD 34.1). For the year of death it was 50.4 (SD 33.1) vii. 36.3 (SD 27.0), respectivelly. Thus the choice of primary chemotherapy whether conventional or more aggressive had no influence on the actual number of in-patient hospital days concerned. When the combination chemotherapy schedule is well tolerated it can be administered just as well on an ambulatory basis or by using it with very short admissions. It seems that the need for inpatient care for patients with multiple myeloma is mostly related to the complications of the disease itself and to intercurrent disorders including infections.

12.
J Infect ; 11(2): 139-44, 1985 Sep.
Article in English | MEDLINE | ID: mdl-4056448

ABSTRACT

Twelve patients who had recovered from pneumococcal infections and 12 household controls were given a polyvalent pneumococcal vaccine. Adequate amounts of antibody were detected by radioimmunoassay before immunisation in controls and patients. More controls responded to nine pneumococcal polysaccharides than did patients. A transient state of unresponsiveness to vaccine may exist in some patients for a period of 4-6 weeks after infection. The high concentrations of antibody before immunisation in adult controls suggest adequate herd immunity to the endemic serotypes in the adult population.


Subject(s)
Antibodies, Bacterial/analysis , Pneumococcal Infections/prevention & control , Vaccination , Adolescent , Adult , Child , Female , Humans , Immunoglobulin A/analysis , Immunoglobulin G/analysis , Immunoglobulin M/analysis , Male , Meningitis, Pneumococcal/immunology , Nigeria , Pneumococcal Infections/immunology , Pneumonia, Pneumococcal/immunology , Serotyping , Streptococcus pneumoniae/classification , Streptococcus pneumoniae/immunology
13.
Am J Otolaryngol ; 6(3): 173-84, 1985.
Article in English | MEDLINE | ID: mdl-3893185

ABSTRACT

A total of 3,340 infants, 95 per cent of them 7 to 9 months old, were randomly vaccinated in a double-blind fashion with either the 14-valent pneumococcal (Pn) polysaccharide vaccine or a saline placebo in three urban areas in Finland. The second dose of the vaccine was given 5 months later. Age and sex distribution, recruitment of infants, and their otitis-related treatment and follow-up were similar in the study areas. Side effects after vaccination were mild and fewer than among older children. Antibody responses to vaccine polysaccharides varied from type to type, but were generally poor, especially to types most prevalent in otitis media. After the first dose of vaccine, the occurrence of otitis visits among the Pn-vaccinated, as compared with controls, showed inter-area differences, but ranged from not more than a 30 per cent reduction at its best to an increase in some areas and in some clinical categories. The respective figures for children with acute otitis media were similar between the vaccination groups and the study areas. The effect of the vaccine on acute otitis media caused by specific Pn types/groups represented in the vaccine was variable but generally poor. Group 6 attacks especially seemed to behave problematically. The second dose of the vaccine did not give additional benefit serologically or clinically. The efficacy of currently available pneumococcal vaccine against otitis media seemed poor in infants.


Subject(s)
Bacterial Vaccines/administration & dosage , Otitis Media/prevention & control , Pneumococcal Infections/prevention & control , Streptococcus pneumoniae/immunology , Antibodies, Bacterial/analysis , Bacterial Vaccines/immunology , Bacteriological Techniques , Clinical Trials as Topic , Double-Blind Method , Female , Finland , Humans , Infant , Male , Otitis Media/immunology , Otitis Media with Effusion/prevention & control , Pneumococcal Infections/immunology , Pneumococcal Vaccines
14.
Pediatrics ; 60(5): 730-7, 1977 Nov.
Article in English | MEDLINE | ID: mdl-335348

ABSTRACT

A recently developed Haemophilus influenzae type b capsular polysaccharide vaccine was given to 48,977 children 3 months to 5 years of age; an equal number of children receiving group A meningococcal vaccine served as controls. The protection as well as serum antibody response was strongly age-dependent. Among children who had received the H. influenzae type b vaccine when 18 months of age or older, there were no cases of bacteremic disease caused by H. influenzae type b in the first year after vaccination. At the same time 11 such cases were seen in the control group of the same age, a highly significant difference. In the second year after vaccination two cases occurred in the H. influenzae type b-vaccinated group, five in the meningococcal-group A vaccinated group. No protection was seen among children who had been younger than 18 months when vaccinated, even if they received a booster dose of the vaccine. The serum antibody response to the H. influenzae type b polysaccharide, measured by radioimmunoassay, was poor in children below 18 months of age and good in those above it. No effect of the vaccine could be seen on the nasopharyngeal carriage of H. influenzae type b, which was approximately 6% in this age group. Adverse effects of the vaccine were mild.


Subject(s)
Bacterial Vaccines , Haemophilus Infections/prevention & control , Haemophilus influenzae/immunology , Polysaccharides, Bacterial/immunology , Antibodies, Bacterial , Bacterial Vaccines/adverse effects , Child, Preschool , Clinical Trials as Topic , Double-Blind Method , Finland , Haemophilus Infections/immunology , Humans , Immunity , Infant , Nasopharynx/microbiology
15.
N Engl J Med ; 297(13): 686-91, 1977 Sep 29.
Article in English | MEDLINE | ID: mdl-408682

ABSTRACT

We performed field trials in the course of an epidemic in Finland to learn whether Group A memingococcal capsular polysaccharide vaccine protects infants and young children from meningitis. The first trial involved 130,178 children between the ages of three months and five years; 49,295 children received the vaccine, 48,977 received a control Haemophilus influenzae Type b polysaccharide vaccine, and 31.906 remained unvaccinated. No cases of meningitis or sepsis caused by Group A meningococci were seen in the first year of observation among the children vaccinated with meningococcal vaccine whereas six occurred among those vaccinated with the H. influenzae vaccine and 13 among those not vaccinated. In the second trial 21,007 children of the same ages received the meningococcal vaccine. No cases caused by Group A occurred among those vaccinated, although five to seven would have been expected within the year. Meningococcal Group A vaccine appears efficacious in young infants and children.


Subject(s)
Bacterial Vaccines , Meningitis, Meningococcal/prevention & control , Neisseria meningitidis/immunology , Polysaccharides, Bacterial/immunology , Antibodies, Bacterial/analysis , Bacterial Vaccines/adverse effects , Child, Preschool , Clinical Trials as Topic , Finland , Haemophilus influenzae/immunology , Humans , Infant , Meningitis, Meningococcal/epidemiology , Vaccination/adverse effects
16.
Duodecim ; 83(19): 1074-80, 1967.
Article in Finnish | MEDLINE | ID: mdl-5584402

Subject(s)
Ribosomes
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