Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 28
Filter
1.
Scand J Rheumatol ; 47(1): 71-78, 2018 Jan.
Article in English | MEDLINE | ID: mdl-28812414

ABSTRACT

OBJECTIVES: Available evidence suggests that genetic factors and overweight play major roles in the aetiology of osteoarthritis (OA). We analysed the association of 18 single-nucleotide polymorphisms (SNPs) from nine adipokine and adipokine receptor genes (LEP, LEPR, ADIPOQ, RETN, NAMPT, SERPINA12, ITLN1, RARRES2, and APLN) with radiographic hand OA. METHOD: The study design was cross-sectional. Bilateral hand radiographs of 542 occupationally active Finnish female dentists and teachers aged 45-63 years were examined and classified for the presence of hand OA using reference images. Hand OA was defined as at least three finger joints with radiographic OA of grade 2-4. The genotypes were determined using polymerase chain reaction-based methods. Body mass index (BMI) was calculated based on self-reported height and measured weight. Associations of the individual SNPs and their haplotypes with hand OA were tested using logistic regression analysis. RESULTS: The minor allele of RETN rs10401670 was associated with a decreased [odds ratio (OR) = 0.73, 95% confidence interval (CI) 0.55-0.97, p = 0.03] and RARRES2 rs4721 with an increased (OR 1.41, 95% CI 1.07-1.87, p = 0.01) prevalence of hand OA. Also, LEPR AC (OR 1.54, 95% CI 1.01-2.35, p = 0.05) and RETN GGTT (OR 0.58, 95% CI 0.37-0.93, p = 0.02) haplotypes were associated with hand OA. These associations were modified by BMI when comparing normal and overweight women. However, the associations lost their statistical significance after adjusting for multiple testing. CONCLUSION: Our results suggest weak associations between the studied variations in LEPR, RARRES2, and RETN genes and hand OA in Finnish women, and that the associations are modified by BMI. However, these associations could not be verified in the current study.


Subject(s)
Adipokines/genetics , Osteoarthritis/genetics , Alleles , Cross-Sectional Studies , Female , Finland , Genetic Predisposition to Disease , Genotype , Hand/pathology , Humans , Middle Aged , Polymerase Chain Reaction , Polymorphism, Single Nucleotide
2.
Phys Rev Lett ; 117(14): 147201, 2016 Sep 30.
Article in English | MEDLINE | ID: mdl-27740785

ABSTRACT

We report a spin valve with a few-layer graphene flake bridging highly spin-polarized La_{0.67}Sr_{0.33}MnO_{3} electrodes, whose surfaces are kept clean during lithographic definition. Sharp magnetic switching is verified using photoemission electron microscopy with x-ray magnetic circular dichroism contrast. A naturally occurring high interfacial resistance ∼12 MΩ facilitates spin injection, and a large resistive switching (0.8 MΩ at 10 K) implies a 70-130 µm spin diffusion length that exceeds previous values obtained with sharp-switching electrodes.

3.
New Microbes New Infect ; 9: 50-3, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26862435

ABSTRACT

Bloodstream recurrent infections have been reported for a variety of opportunistic bacteria. These are often either catheter related or are caused by indwelling devices. A case of relapsing sepsis with two Escherichia coli strains carrying extended-spectrum ß-lactamase and derepressed ampC genes is reported. The patient had seven episodes of bloodstream infections within 1 year and was diagnosed with chronic autoimmune pancreatitis and IgG4 hypergammaglobulinaemia. Abscesses were found in his spleen and pancreas cauda, which was finally resected. Relapses of bacteraemia with resistant enterobacteria should be considered during perioperative protection. Surgical removal of the infective focus could be curative.

4.
Scand J Immunol ; 82(6): 539-46, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26346780

ABSTRACT

There is an increasing need for novel biomarkers that enable better diagnostic and prognostic stratification of patients with suspected infection. A proprotein convertase enzyme FURIN is upregulated upon immune cell activation, and it promotes infectivity by cleaving and activating pathogens. In this study, we determined FURIN levels in plasma using ELISA from 537 patients that were admitted to emergency room with suspected infection. Patients were sorted to high- and low-level FURIN groups with a cut-off level of 370 pg/ml. The study cohort included five diagnostic groups: Group 1, no systemic inflammatory response syndrome (SIRS, n = 59 patients); Group 2, bacterial infection without SIRS (n = 67); Group 3, SIRS, but no bacterial infection (n = 308); Group 4, sepsis without organ failure (n = 308); and Group 5, severe sepsis (n = 49). Statistically significant associations were not found between the plasma level of FURIN and the prevalence of sepsis (P = 0.957), diagnostic group of a patient (P = 0.737) or the bacteria in blood culture (P = 0.499). Additionally, the concentration of FURIN did not predict the severity or case fatality of the infectious disease. However, statistically significant associations were found between high plasma level of FURIN and diagnosed rheumatic disease (P < 0.001) as well as with the prevalence of non-smokers (P = 0.034). Thus, albeit the plasma level of FURIN does not predict the severity of infectious disease, it may be of use in the diagnostics of autoimmune diseases.


Subject(s)
Autoimmune Diseases/diagnosis , Bacterial Infections/diagnosis , Furin/blood , Sepsis/diagnosis , Adolescent , Adult , Aged , Aged, 80 and over , Autoimmune Diseases/blood , Bacterial Infections/blood , Bacterial Infections/complications , Biomarkers/blood , Emergency Service, Hospital , Female , Humans , Male , Middle Aged , Prospective Studies , Rheumatic Diseases/blood , Sepsis/blood , Sepsis/complications , Young Adult
5.
Strahlenther Onkol ; 189(11): 951-6, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23999735

ABSTRACT

OBJECTIVE: The goal of this work was to evaluate whether the volume reduction related to removal of gas in the rectum could be translated in lower doses to organs at risk (OAR) during vaginal cuff brachytherapy (VBT). MATERIAL AND METHODS: Fourteen pairs of brachytherapy planning CT scans derived from 11 patients were re-segmented and re-planned using the same parameters. The only difference between pairs of CTs was the presence or lack of gas in the rectum. The first CT showed the basal status and the second was carried out after gas removal with a tube. A set of values derived from bladder and rectum dose-volume histograms (DVH) and dose-surface histograms (DSH) were extracted. Moreover the cylinder position related to the patient craniocaudal axis was recorded. RESULTS: Rectum volume decreased significantly from 77.8 ± 45 to 55.43 ± 17.6 ml (p = 0.0052) after gas removal. Such volume diminution represented a significant reduction on all rectal DVH parameters analyzed except D25 % and D50 %. DSH parameter results were similar to previous ones. A nonsignificant increase of the bladder volume was observed and was associated with an increase of the DVH metrics analyzed. CONCLUSION: Removal of gas pockets is a simple and inexpensive maneuver that decreases rectal dose parameters on VBT, which can be translated as a better therapeutic ratio. It also suggests that other actions directed to empty the rectum could have a similar effect.


Subject(s)
Brachytherapy/instrumentation , Gases/isolation & purification , Radiation Protection/methods , Radiotherapy Dosage , Rectum/chemistry , Rectum/diagnostic imaging , Vaginal Neoplasms/radiotherapy , Brachytherapy/methods , Female , Humans , Organ Size , Organs at Risk , Prosthesis Design , Radiography , Radiotherapy Planning, Computer-Assisted/methods , Treatment Outcome , Vaginal Neoplasms/diagnostic imaging
6.
Eur Respir J ; 38(3): 672-8, 2011 Sep.
Article in English | MEDLINE | ID: mdl-20847076

ABSTRACT

The objective of this study was to determine whether genetic polymorphisms in enzymes that metabolise oxidative agents modify the individual susceptibility to developing asbestos and smoking-related pleuropulmonary changes. Nine polymorphisms of six genes (EPHX1, GSTM1, GSTM3, GSTP1, GSTT1 and NAT2) were genotyped from 1,008 Finnish asbestos-exposed workers. The genotype data were compared to signs of lung fibrosis and pleural thickenings, as well as with total lung capacity, single-breath diffusing capacity of the lung for carbon monoxide (D(L,CO)) and specific diffusing capacity (expressed as D(L,CO) per unit of alveolar volume (V(A))). The GSTT1 deletion polymorphism was associated with fibrotic changes (p=0.003), and decreased D(L,CO) (p=0.02) and D(L,CO)/V(A) (p=0.002), and the GSTM1 deletion polymorphism was associated with the greatest thickness of pleural plaques (p=0.009). On further analysis, the GSTT1 null genotype was found to pose over a three-fold risk for severe fibrotic changes (OR 3.12, 95% CI 1.51-6.43), and around two-fold risks for decreased D(L,CO) (OR 1.77, 95% CI 1.06-2.95) and D(L,CO)/V(A) (OR 2.37, 95% CI 1.33-4.23). In addition, the GSTM1 null genotype showed an elevated risk (OR 1.36, 95% CI 1.03-1.80) for thicker pleural plaques. Our data suggest that inherited detoxification capacity may affect the development and severity of asbestos and smoking-related nonmalignant pulmonary changes.


Subject(s)
Asbestos/toxicity , Genetic Predisposition to Disease , Lung Diseases/chemically induced , Lung Diseases/genetics , Pulmonary Fibrosis/chemically induced , Pulmonary Fibrosis/genetics , Aged , Female , Fibrosis , Gene Deletion , Genotype , Glutathione Transferase/genetics , Humans , Lung/pathology , Lung Diseases/diagnosis , Male , Middle Aged , Occupational Exposure , Polymorphism, Genetic , Pulmonary Fibrosis/diagnosis , Quality Control , Risk Factors , Xenobiotics/therapeutic use
7.
Ann Rheum Dis ; 68(10): 1633-7, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19019890

ABSTRACT

OBJECTIVES: To study the role of two COL2A1 single nucleotide polymorphisms (rs3737548 and rs2276455) and their haplotypes in individual susceptibility to osteoarthritis (OA) of the hand in Finnish women. METHODS: Bilateral hand radiographs of 543 Finnish female dentists and teachers aged 45-63 years were examined and classified for the presence of OA by using reference images. The COL2A1 genotypes were determined by PCR-based methods. Data regarding other risk factors were collected by questionnaire. The haplotypes were statistically reconstructed from the genotype data by the PHASE program. Associations between the genotypes/diplotypes and hand OA were studied by logistic regression. RESULTS: Allowing for age and occupation, the carriage of at least one COL2A1 intron 33 minor allele was associated with an increased risk of hand OA (odds ratio (OR) 1.58, 95% CI 1.05 to 2.36) and the number of affected joints. When stratified by occupation, the increased risk associated with the intron 33 minor allele carriage appeared to be mainly attributable to the dentists (OR 2.18, 95% CI 1.18 to 4.06). The 2-1 haplotype (exon 5B minor allele-intron 33 major allele) posed a significantly higher risk of hand OA (OR 3.21, 95% CI 1.08 to 9.55) compared with non-carriers. Moreover, an interaction was observed between intron 33 minor allele carriage and low task variation history in dental work (OR 2.87, 95% CI 1.05 to 7.89 for their joint effect). CONCLUSIONS: The results suggest that the studied COL2A1 gene polymorphisms may play a role in the aetiology of hand OA and that this effect may be enhanced by repetitive loading work tasks.


Subject(s)
Collagen Type II/genetics , Hand Joints , Occupational Diseases/genetics , Osteoarthritis/genetics , Polymorphism, Single Nucleotide , Cumulative Trauma Disorders/complications , Cumulative Trauma Disorders/epidemiology , Cumulative Trauma Disorders/genetics , Dentists, Women/statistics & numerical data , Female , Finland/epidemiology , Genetic Predisposition to Disease , Genotype , Humans , Middle Aged , Occupational Diseases/diagnostic imaging , Occupational Diseases/epidemiology , Osteoarthritis/epidemiology , Osteoarthritis/etiology , Prevalence , Radiography
8.
HIV Med ; 10(1): 1-5, 2009 Jan.
Article in English | MEDLINE | ID: mdl-18795963

ABSTRACT

OBJECTIVE: To study the relationship between antiretroviral (ARV) treatment and abnormal ankle-branch index (ABI) and to compare the risk factors for altered ABI. METHODS: Patients coming to the office from April 2007 until July 2007 were offered the chance to take part in the study. ABI was obtained by the standard technique. Those < or = 0.9 or > or = 1.3 were considered altered ABI. Clinical reports were reviewed to examine traditional vascular risk factors, coinfection with hepatitis C virus and/or hepatitis B virus, tobacco use, highly active antiretroviral therapy use and its components and length of use of each ARV drug. RESULTS: ABI was measured in 147 patients, 82.3% males. Thirty-three patients (22.45%) had an altered ABI, and it was related to CD4 cell nadir, dyslipidaemia and protease inhibitor (PI) use. When logistic regression was carried out, only dyslipidaemia (OR 2.68, CI 95%: 1.06-6.91) and PI use (OR 2.79, CI 95%: 1.15-6.54) remained in the model. CONCLUSIONS: Altered ABI is associated with PI use independently of dyslipidaemia. Probably, it marks patients with high vascular risk not identified with traditional scales.


Subject(s)
Ankle Brachial Index/methods , Ankle/blood supply , Dyslipidemias/etiology , HIV Infections/complications , HIV-1 , Peripheral Vascular Diseases/etiology , Adult , Antiretroviral Therapy, Highly Active , Blood Pressure/physiology , Brachial Artery/drug effects , Dyslipidemias/physiopathology , Female , HIV Infections/drug therapy , HIV Infections/physiopathology , HIV Protease Inhibitors/adverse effects , HIV-1/drug effects , Humans , Male , Peripheral Vascular Diseases/physiopathology , Risk Assessment
SELECTION OF CITATIONS
SEARCH DETAIL
...