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1.
Br J Dermatol ; 184(1): 14-24, 2021 01.
Article in English | MEDLINE | ID: mdl-32628773

ABSTRACT

Psoriasis is a chronic inflammatory disease with a strong genetic component that can be triggered by environmental factors. Disease pathogenesis is mainly driven by type 1 and type 17 cytokine-producing cells which, in healthy individuals, are modulated by regulatory T cells (Tregs). Tregs play a fundamental role in immune homeostasis and contribute to the prevention of autoimmune disease by suppressing immune responses. In psoriasis, Tregs are impaired in their suppressive function leading to an altered T-helper 17/Treg balance. Although Treg dysfunction in patients with psoriasis is associated with disease exacerbation, it is unknown how they are functionally regulated. In this review, we discuss recent insights into Tregs in the setting of psoriasis with an emphasis on the effect of current treatments on Tregs and how already available therapeutics that modulate Treg frequency or functionality could be exploited for treatment of psoriasis.


Subject(s)
Autoimmune Diseases , Psoriasis , Cytokines , Disease Progression , Humans , Psoriasis/therapy , T-Lymphocytes, Regulatory
2.
Eur Child Adolesc Psychiatry ; 29(1): 29-39, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31227911

ABSTRACT

There is very limited information available on child and adolescent psychiatry (CAP) training in the Southeast European (SEE) region. The objective of this study was to fill in this gap by presenting descriptive data on CAP training and national mental health services for children and adolescent in 11 SEE countries. On the initiative of World Psychiatric Association-CAP section, national CAP association boards from each SEE country allocated one member to the Consortium on Academic Child and Adolescent Psychiatry in SEE (CACAP SEE) in 2018. Using an internally distributed questionnaire, CACAP SEE members provided information on the CAP training structure and mental health care. Ten out of eleven SEE countries recognized CAP as a separate specialty. Duration of training did not differ much between the SEE countries. Other components were more variable (availability of rotations, overseas electives, and inclusion of psychotherapy). Ten countries were familiar with the CAP requirements of the European Union of Medical Specialists (UEMS-CAP) and five provided the training in accordance with it. Nine countries had less than 36 board-certified child and adolescent psychiatrists practicing in the country. The number of general psychiatrists treating children and adolescents with mental disorders was higher than the number of CAP specialists in five of the countries. Although CAP was recognized as a separate specialty in the vast majority of SEE countries, there was a substantial variation among them in available CAP training. In most of the countries, there is a considerable lack of CAP specialists for several reasons, including loss of trained specialists to other countries.


Subject(s)
Adolescent Psychiatry/education , Child Psychiatry/education , Education, Medical/methods , Mental Health/education , Adolescent , Adult , Child , Europe , Female , Humans , Male , Young Adult
3.
Epidemiol Psychiatr Sci ; 26(4): 430-440, 2017 Aug.
Article in English | MEDLINE | ID: mdl-27353487

ABSTRACT

BACKGROUND: In order to compare estimates by one assessment scale across various cultures/ethnic groups, an important aspect that needs to be demonstrated is that its construct across these groups is invariant when measured using a similar and simultaneous approach (i.e., demonstrated cross-cultural measurement invariance). One of the methods for evaluating measurement invariance is testing for differential item functioning (DIF), which assesses whether different groups respond differently to particular items. The aim of this study was to evaluate the cross-cultural measurement invariance of the Revised Child Anxiety and Depression Scale (RCADS) in societies with different socioeconomic, cultural, and religious backgrounds. METHODS: The study was organised by the International Child Mental Health Study Group. Self-reported data were collected from adolescents residing in 11 countries: Brazil, Bulgaria, Croatia, Indonesia, Montenegro, Nigeria, Palestinian Territories, the Philippines, Portugal, Romania and Serbia. The multiple-indicators multiple-causes model was used to test the RCADS items for DIF across the countries. RESULTS: Ten items exhibited DIF considering all cross-country comparisons. Only one or two items were flagged with DIF in the head-to-head comparisons, while there were three to five items flagged with DIF, when one country was compared with the others. Even with all cross-culturally non-invariant items removed from nine language versions tested, the original factor model representing six anxiety and depressive symptoms subscales was not significantly violated. CONCLUSIONS: There is clear evidence that relatively small number of the RCADS items is non-invariant, especially when comparing two different cultural/ethnic groups, which indicates on its sound cross-cultural validity and suitability for cross-cultural comparisons in adolescent anxiety and depressive symptoms.


Subject(s)
Adolescent Psychiatry/standards , Anxiety/diagnosis , Child Psychiatry/standards , Cross-Cultural Comparison , Depression/diagnosis , Language , Psychiatric Status Rating Scales/standards , Adolescent , Adolescent Psychiatry/methods , Child , Child Psychiatry/methods , Female , Humans , Male , Psychometrics , Quality of Life/psychology , Reproducibility of Results , Surveys and Questionnaires
4.
J Vet Intern Med ; 29(4): 1069-73, 2015.
Article in English | MEDLINE | ID: mdl-26118570

ABSTRACT

BACKGROUND: The prevalence of concurrent disease in hyperthyroid cats is unknown. OBJECTIVES: To identify the prevalence of concurrent intra-abdominal disease using abdominal ultrasound examination (AUS) in hyperthyroid cats referred for radioactive iodine treatment (RIT) and to determine whether the requirement for pretreatment AUS is justified. ANIMALS: Five hundred and thirty-four client-owned cats diagnosed with hyperthyroidism and referred for RIT. METHODS: Retrospective study. Age, breed, sex, body weight, clinical signs, total serum T4 concentration, blood urea nitrogen (BUN) concentration, serum creatinine concentration, urine specific gravity (USG), AUS results, and biopsy or cytology results, or both (if obtained) were collected from the medical records. RESULTS: The prevalence of concurrent disease identified using AUS in hyperthyroid cats referred for RIT was 36.1%; 22.8% of the cats in the study had renal disease and 2.4% had confirmed neoplasia. Significant differences in median USG (P value 0.032) and median BUN (P value 0.028) were found between cats that had abnormal kidneys on AUS compared to those with normal-appearing kidneys. Only 2.2% of the cats were not treated with RIT as a result of changes identified on AUS and subsequently obtained cytology or biopsy results. CONCLUSIONS AND CLINICAL IMPORTANCE: The results indicate that pretreatment AUS in hyperthyroid cats referred for RIT is unnecessary in most patients.


Subject(s)
Cat Diseases/diagnostic imaging , Hyperthyroidism/veterinary , Iodine Radioisotopes/therapeutic use , Abdomen/diagnostic imaging , Animals , Cat Diseases/radiotherapy , Cats , Female , Hyperthyroidism/complications , Hyperthyroidism/diagnostic imaging , Hyperthyroidism/radiotherapy , Kidney Diseases/complications , Kidney Diseases/diagnostic imaging , Kidney Diseases/veterinary , Male , Retrospective Studies , Ultrasonography
5.
Am J Ophthalmol ; 127(2): 142-7, 1999 Feb.
Article in English | MEDLINE | ID: mdl-10030554

ABSTRACT

PURPOSE: To determine the effect on serum lipid levels of carteolol hydrochloride 1.0% or timolol maleate 0.5% given twice a day to women age 60 years and older with primary open-angle glaucoma or ocular hypertension. METHOD: We included 112 patients in this double-masked, randomized, multicenter trial. Fasting clinical laboratory studies were evaluated at baseline and at 12 weeks. Patients were instructed not to change their dietary, alcohol consumption, or exercise habits during the study. RESULTS: For the carteolol group, the high-density lipoprotein (HDL) and total cholesterol/high-density lipoprotein (TC/HDL) ratio at baseline of 50.1 +/- 1.5 mg/dl and 4.7 +/- 0.2 changed by the 12-week visit to 51.3 +/- 1.9 mg/dl (P = .25) and 4.6 +/- .02 (P = .47), respectively. For the timolol maleate group, the baseline HDL and TC/HDL ratio of 53.6 +/- 2.2 mg/dl and 4.4 +/- 0.2 changed to 50.2 +/- 1.9 mg/dl (P < .001) and 4.7 +/- 0.2 (P = .001), respectively, at the 12-week visit. Carteolol patients showed no significant change from baseline, whereas the HDL (P < .001) and TC/HDL ratio decreased (P = .001) significantly in the timolol maleate group. There also was a significant difference in the change from baseline at 12 weeks between carteolol and timolol maleate groups for the HDL and TC/HDL ratio (P = .01 and .012, respectively). No differences in TC, low-density lipoprotein (LDL), or triglycerides (TG) or in changes from baseline were observed between groups at 12 weeks (P > .05). At 12 weeks, no differences were observed between carteolol and timolol maleate groups in intraocular pressure or safety (P > .05), except that patients given carteolol demonstrated fewer solicited ocular symptoms (P = .007). CONCLUSIONS: Carteolol appears to be neutral in its effect on serum lipid levels, whereas timolol maleate adversely affects the HDL and TC/HDL ratio in women age 60 years and older with ocular hypertension or primary open-angle glaucoma.


Subject(s)
Adrenergic beta-Antagonists/therapeutic use , Carteolol/therapeutic use , Glaucoma, Open-Angle/drug therapy , Lipids/blood , Ocular Hypertension/drug therapy , Timolol/therapeutic use , Adrenergic beta-Antagonists/administration & dosage , Adrenergic beta-Antagonists/adverse effects , Aged , Aged, 80 and over , Carteolol/administration & dosage , Carteolol/adverse effects , Double-Blind Method , Female , Glaucoma, Open-Angle/blood , Humans , Middle Aged , Ocular Hypertension/blood , Ophthalmic Solutions/administration & dosage , Ophthalmic Solutions/adverse effects , Ophthalmic Solutions/therapeutic use , Prospective Studies , Timolol/administration & dosage , Timolol/adverse effects
6.
Am J Ophthalmol ; 124(4): 498-505, 1997 Oct.
Article in English | MEDLINE | ID: mdl-9323940

ABSTRACT

PURPOSE: To evaluate the ocular hypotensive effect and safety of carteolol hydrochloride 1% vs timolol maleate 0.5%. METHODS: One hundred seventy-six patients with ocular hypertension or primary open-angle glaucoma were randomly assigned to receive either carteolol 1% twice a day or timolol maleate 0.5% solution twice a day in a randomized, double-masked, multicenter, parallel-group, active-control comparison trial during a 3-month period. RESULTS: After 12 weeks, carteolol 1% reduced the mean +/- SE intraocular pressure from 25.0 +/- 0.3 to 19.5 +/- 0.3 mm Hg; timolol maleate 0.5% reduced the mean intraocular pressure from 25.2 +/- 0.3 to 19.6 +/- 0.3 mm Hg. The mean difference in trough intraocular pressure between carteolol and timolol maleate of -0.14 mm Hg was not significantly (P = .745) different (95% confidence limits, -0.97 to 0.70 mm Hg). Trough pulse and blood pressure also showed no consistent statistically significant differences between groups. The 2-hour postdose pulse, however, demonstrated a greater decrease in the timolol maleate than in the carteolol group (P < .001). Systemic and ocular signs and symptoms were similar between the groups except that the number of treatment-emergent reports of bradycardia was greater in the timolol maleate group (P = .039), and the carteolol group reported fewer ocular symptoms than the timolol maleate group did (P < .01). CONCLUSIONS: Both carteolol 1% and timolol maleate 0.5% are highly effective in lowering intraocular pressure when measured at the end of the dosing interval. Carteolol 1% demonstrates an ocular hypotensive effect and safety profile similar to those of timolol maleate 0.5% solution.


Subject(s)
Adrenergic beta-Antagonists/therapeutic use , Carteolol/therapeutic use , Intraocular Pressure/drug effects , Ocular Hypertension/drug therapy , Timolol/therapeutic use , Adolescent , Adrenergic beta-Antagonists/adverse effects , Adult , Aged , Aged, 80 and over , Carteolol/adverse effects , Double-Blind Method , Female , Humans , Male , Middle Aged , Ocular Hypertension/physiopathology , Timolol/adverse effects , Treatment Outcome
7.
Am J Ophthalmol ; 123(4): 465-77, 1997 Apr.
Article in English | MEDLINE | ID: mdl-9124243

ABSTRACT

PURPOSE: To compare the effects of topical timolol maleate 0.5% and carteolol hydrochloride 1% on pulse rate and blood pressure. METHODS: In a randomized, double-masked, parallel-design, multicenter clinical trial, we compared the effects of timolol and carteolol on pulse rate and blood pressure measured by 24-hour ambulatory blood pressure monitoring in 169 adult patients with either ocular hypertension or primary open-angle glaucoma. RESULTS: From noon to 8 PM, baseline mean pulse rate of 82 to 83 beats per minute (bpm) had decreased by 4 to 6 bpm in both groups after 4 weeks of therapy with timolol or carteolol. From midnight to 4 AM, the pulse rate in the carteolol group was significantly above baseline (P = .005), while the timolol group was significantly below baseline (P < .001). Four times as many patients became bradycardic (heart rate, < 60 bpm) on timolol (18.4%) as did patients on carteolol (4.5%) from midnight to 4 AM. More than twice as many patients exhibited a resolution of their bradycardia with carteolol (46.7%) as did patients treated with timolol (18.2%) from midnight to 4 AM. Overall cardiovascular adverse effects were reported significantly more frequently in the timolol than the carteolol group (P = .002). CONCLUSIONS: Timolol causes significantly lower mean heart rate during the nighttime and more nocturnal bradycardia than carteolol does in patients with ocular hypertension and primary open-angle glaucoma. These differences may be because of the intrinsic sympathomimetic activity of carteolol.


Subject(s)
Adrenergic beta-Antagonists/therapeutic use , Blood Pressure/drug effects , Carteolol/therapeutic use , Glaucoma, Open-Angle/drug therapy , Heart Rate/drug effects , Ocular Hypertension/drug therapy , Timolol/therapeutic use , Administration, Topical , Adrenergic beta-Antagonists/administration & dosage , Adrenergic beta-Antagonists/adverse effects , Adult , Aged , Blood Pressure/physiology , Blood Pressure Monitoring, Ambulatory , Carteolol/administration & dosage , Carteolol/adverse effects , Double-Blind Method , Female , Glaucoma, Open-Angle/physiopathology , Heart Rate/physiology , Humans , Male , Middle Aged , Ocular Hypertension/physiopathology , Ophthalmic Solutions , Timolol/administration & dosage , Timolol/adverse effects , Visual Acuity
8.
Brain Cogn ; 21(1): 1-19, 1993 Jan.
Article in English | MEDLINE | ID: mdl-8424858

ABSTRACT

This article reports the neuropsychological sequelae of Wernicke's Encephalopathy in a 20-year-old woman. After amelioration of acute symptoms, the patient showed a range of cognitive impairments the most marked of which was a severe impairment on free recall tasks involving both verbal and nonverbal material. In contrast, recognition memory appeared remarkably well preserved. Some evidence of frontal lobe and general intellectual impairment was also noted. The case is discussed in terms of the pathophysiology of Wernicke-Korsakoff Syndrome, criteria for its diagnosis, and the multicomponent nature of memory deficits.


Subject(s)
Frontal Lobe/physiopathology , Mental Recall/physiology , Neuropsychological Tests , Wernicke Encephalopathy/psychology , Adult , Alcohol Amnestic Disorder/physiopathology , Alcohol Amnestic Disorder/psychology , Anorexia Nervosa/physiopathology , Anorexia Nervosa/psychology , Bulimia/physiopathology , Bulimia/psychology , Female , Humans , Memory, Short-Term/physiology , Neurologic Examination , Tomography, X-Ray Computed , Wernicke Encephalopathy/physiopathology
11.
J Pediatr ; 92(2): 188-93, 1978 Feb.
Article in English | MEDLINE | ID: mdl-621601

ABSTRACT

A prospective study was conducted in children with urinary tract infections to examine the relationship between the presence of antibody-coated bacteria in the urinary sediments and the presence of pyelonephritis. The site of the urinary tract infection was localized as upper or lower urinary tract by the bladder washout technique. Antibody-coated bacteria in the urinary sediments were identified by an immunofluorescent method. In 4 of 12 children with upper urinary tract infections, less than 1% of the bacteria in the urinary sediments were antibody coated. In 10 of 35 children with lower urinary tract infections more than 50% of the bacteria in the urinary sediments were antibody coated. These studies show no significant correlation between the presence of antibody-coated bacteria in urinary sediments and infection of the upper urinary tract.


Subject(s)
Antibodies, Bacterial/urine , Bacteria/immunology , Urinary Tract Infections/diagnosis , Adolescent , Child , Child, Preschool , Female , Humans , Male
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