Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 71
Filter
1.
HIV Med ; 22(8): 674-681, 2021 09.
Article in English | MEDLINE | ID: mdl-34288357

ABSTRACT

BACKGROUND: Persistent inflammation and immune activation are associated with lymph node fibrosis and end-organ diseases in treatment-suppressed people living with HIV (PLWH). We investigated the effect of switching to raltegravir and/or adding losartan on lymphoid tissue fibrosis and on the inflammatory/immune-activation mediators in treated HIV patients. METHODS: Chronic HIV-infected patients treated with two nucleoside reverse transcriptase inhibitors (2NRTI) and one non-NRTI (NNRTI) or protease inhibitor (PI) during at least 48 weeks were randomized to four groups (n = 48): 2NRTI + efavirenz (EFV), 2NRTI + EFV + losartan, 2NRTI + raltegravir and 2NRTI + raltegravir + losartan for 48 weeks. Tonsillar biopsy and peripheral blood markers of CD4 and CD8 T-lymphocyte activation and senescence, monocyte activation and soluble markers of inflammation were determined at baseline and at week 48 and compared between groups. RESULTS: No changes in lymphoid tissue architecture were observed. Adding losartan had no impact on lymphocyte subsets. Conversely, patients who switched to raltegravir showed a higher decrease in all activated [CD4+CD38+HLA-DR+, -0.3 vs. 0.48 (P = 0.033); CD8+CD38+ HLA-DR+, -1.6 vs. 1.3 (P = 0.02)] and senescent [CD4+CD28-CD57+, -0.3 vs. 0.26 (P = 0.04); CD8+CD28-CD57+, -6.1 vs. 3.8 (P = 0.002)] T lymphocytes. In addition, the median CD4/CD8 ratio increased by 0.35 in patients in the raltegravir group vs. 0.03 in the other arms (P = 0.002). Differences between groups in monocyte subpopulations or soluble inflammation markers were not observed. CONCLUSIONS: Losartan had no effect on lymphoid fibrosis or immune activation/inflammation. Conversely, switching to a regimen with raltegravir significantly decreased activated and senescent T-lymphocyte subpopulations and increased CD4/CD8 ratio in successfully treated PLWH.


Subject(s)
Anti-HIV Agents , HIV Infections , Anti-HIV Agents/therapeutic use , Fibrosis , HIV Infections/complications , HIV Infections/drug therapy , Humans , Inflammation/chemically induced , Inflammation/drug therapy , Losartan/therapeutic use , Lymphoid Tissue , Raltegravir Potassium/therapeutic use , Viral Load
2.
Lupus ; 28(4): 555-559, 2019 Apr.
Article in English | MEDLINE | ID: mdl-30755141

ABSTRACT

OBJECTIVE: The objective of this report is to analyse retinal changes over a five-year period, assessed by spectral domain-optical coherence tomography (SD-OCT), in patients from the Lupus-Cruces cohort treated with hydroxychloroquine (HCQ). METHODS: SD-OCT screening was performed annually between 2012 and 2017. Average macular thickness (AMT), ganglion cell layer thickness (GCLT) and qualitative data of retinal pigment epithelium (RPE) and external retina (ExtR) were collected prospectively. We compared data from 2012 (first) and 2017 (second) SD-OCT. RESULTS: We studied 110 patients and 195 eyes. No cases of HCQ toxicity were detected. At the time of the second SD-OCT, 99% patients had taken a daily dose of HCQ ≤5 mg/kg/day. The median time on HCQ was 133 months. The mean AMT and GCLT were significantly lower in both eyes at the second SD-OCT; however, all the differences were clinically insignificant at less than 1%. Qualitative analysis of RPE and ExtR showed no significant changes. Similar results were found among patients with risk factors for retinopathy. The comparison of patients with and without risk factors showed no differences. CONCLUSIONS: This study shows clinically irrelevant retinal changes in an SLE cohort on HCQ treatment over a five-year follow-up. Our findings support the safety of long-term HCQ at doses ≤5 mg/kg/day.


Subject(s)
Antirheumatic Agents/adverse effects , Hydroxychloroquine/adverse effects , Lupus Erythematosus, Systemic/drug therapy , Lupus Erythematosus, Systemic/pathology , Retina/pathology , Adult , Aged , Antirheumatic Agents/administration & dosage , Cohort Studies , Female , Follow-Up Studies , Hospitals, University , Humans , Hydroxychloroquine/administration & dosage , Incidence , Male , Middle Aged , New Mexico/epidemiology , Prospective Studies , Retina/drug effects , Retinal Diseases/chemically induced , Retinal Diseases/pathology , Statistics, Nonparametric , Tomography, Optical Coherence , White People
3.
BJOG ; 126(5): 656-661, 2019 Apr.
Article in English | MEDLINE | ID: mdl-30222236

ABSTRACT

OBJECTIVE: To evaluate the subsequent rate of thrombosis among women with obstetric antiphospholipid syndrome (Ob-APS) in a multicentre database of antiphospholipid antibody (aPL)-positive patients, and the clinical utility of the adjusted Global Antiphospholipid Syndrome Score (aGAPSS), a validated tool to assess the likelihood of developing new thrombosis, in this group of patients. DESIGN: Retrospective study. SETTING: The Antiphospholipid Syndrome Alliance for Clinical Trials and International Networking Clinical Database and Repository. POPULATION: Women with Ob-APS. METHODS: Comparison of clinical and laboratory characteristics and measurement of aGAPSS in women with Ob-APS, with or without thrombosis, after initial pregnancy morbidity (PM). MAIN OUTCOME MEASURES: Risk factors for thrombosis and aGAPSS. RESULTS: Of 550 patients, 126 had Ob-APS; 74/126 (59%) presented with thrombosis, and 47 (63%) of these women developed thrombosis after initial PM, in a mean time of 7.6 ± 8.2 years (4.9/100 patient years). Younger age at diagnosis of Ob-APS, additional cardiovascular risk factors, superficial vein thrombosis, heart valve disease, and multiple aPL positivity increased the risk of first thrombosis after PM. Women with thrombosis after PM had a higher aGAPSS compared with women with Ob-APS alone [median 11.5 (4-16) versus 9 (4-13); P = 0.0089]. CONCLUSION: Based on a retrospective analysis of our multicentre aPL database, 63% of women with Ob-APS developed thrombosis after initial obstetric morbidity; additional thrombosis risk factors, selected clinical manifestations, and high-risk aPL profile increased the risk. Women with subsequent thrombosis after Ob-APS had a higher aGAPSS at entry to the registry. We believe that aGAPSS is a valid tool to improve risk stratification in aPL-positive women. TWEETABLE ABSTRACT: More than 60% of women with obstetric antiphospholipid syndrome had thrombosis after initial pregnancy morbidity.


Subject(s)
Antiphospholipid Syndrome/complications , Pregnancy Complications, Cardiovascular/immunology , Thrombosis/immunology , Adult , Antibodies, Antiphospholipid/blood , Antibodies, Antiphospholipid/immunology , Antiphospholipid Syndrome/blood , Clinical Trials as Topic , Databases, Factual , Female , Humans , Pregnancy , Registries , Retrospective Studies , Risk Factors
4.
Int J Endocrinol ; 2018: 5718782, 2018.
Article in English | MEDLINE | ID: mdl-30363667

ABSTRACT

Infertility and reproductive problems have been reported in women with several neurological disorders, for example, demyelination. However, the physiology of such problems has remained unknown so far. The taiep rats are an animal neurological model that initially shows a hypomyelination followed by a progressive demyelination of the central nervous system. This animal has reproductive problems, and the aim of this work is to characterize the follicular development, secretion of ovarian hormones, and presence of noradrenaline in the ovaries of the female taiep rats in the juvenile and adult stages. The taiep rats have low body weight (approximately 19% less than that of SD rats), a delay of 4 days in the age of vaginal opening, and an irregularity in the estrous cycle by the absence or prolongation of some estral cycle stage. In the juvenile stage, we observed a decrease of approximately 44% in the total number of follicles with a 15% increase of atresia and an 80% decrease in the fluorescence intensity of catecholamines in the ovaries, with a 21% increment in plasma concentrations of testosterone. In the adult stage, we observed follicular cysts and a 50% decrease in fluorescence intensity of catecholamines in the ovaries, with changes in the secretion of ovarian hormones, an increase of 20 times in progesterone, and a decrement of a half in estradiol. The demyelination in taiep rats affects follicular development and steroidogenesis in the early stages of the animal's life, and this is maintained until adulthood.

5.
Lupus ; 27(10): 1718-1722, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29635998

ABSTRACT

Aim The aim of this study was to evaluate the clinical response to combined therapy with hydroxychloroquine and mepacrine in patients with systemic lupus erythematosus and refractory joint and/or skin disease. Methods Mepacrine was added to 46 systemic lupus erythematosus patients unresponsive to treatment with the following drug combinations: hydroxychloroquine + prednisone + immunosuppressive drugs ( n = 24), hydroxychloroquine + prednisone ( n = 16), hydroxychloroquine + prednisone + retinoids ( n = 2), hydroxychloroquine alone ( n = 1), hydroxychloroquine + one immunosuppressive drug ( n = 1), hydroxychloroquine + prednisone + one immunosuppressive drug + belimumab ( n = 1) or hydroxychloroquine + prednisone + belimumab ( n = 1). The outcome variable was the clinical response, either complete or partial, based on clinical judgement. The Cutaneous Lupus Erythematosus Disease Area and Severity Index (CLASI) and the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) score were additionally used. Results A total of 91% patients showed complete/partial response, with similar rates among those with joint or skin disease. In patients with cutaneous activity, a statistically significant decrease in the CLASI was seen. There also was a statistically significant decrease in the SLEDAI. The mean daily dose of prednisone decreased from 5.8 to 3.4 mg/d ( p = 0.001). Prednisone could be discontinued in 20% of patients. No serious adverse events were seen. Smoking was the only predictor of complete response. Conclusion In the setting of refractory skin and/or joint disease, the addition of mepacrine to previous therapy including hydroxychloroquine was safe and effective in reducing disease activity and decreasing prednisone doses. The fact that smokers responded better opens the door to further studying the combination of mepacrine-hydroxychloroquine as a first-line therapy in such patients.


Subject(s)
Antimalarials/therapeutic use , Hydroxychloroquine/therapeutic use , Immunosuppressive Agents/therapeutic use , Joint Diseases/drug therapy , Lupus Erythematosus, Cutaneous/drug therapy , Lupus Erythematosus, Systemic/drug therapy , Quinacrine/therapeutic use , Adult , Antimalarials/adverse effects , Drug Therapy, Combination , Female , Humans , Hydroxychloroquine/adverse effects , Immunosuppressive Agents/adverse effects , Joint Diseases/diagnosis , Joint Diseases/immunology , Lupus Erythematosus, Cutaneous/diagnosis , Lupus Erythematosus, Cutaneous/immunology , Lupus Erythematosus, Discoid/diagnosis , Lupus Erythematosus, Discoid/drug therapy , Lupus Erythematosus, Discoid/immunology , Lupus Erythematosus, Systemic/diagnosis , Lupus Erythematosus, Systemic/immunology , Male , Middle Aged , Quinacrine/adverse effects , Remission Induction , Retrospective Studies , Smokers , Treatment Outcome
6.
Lupus ; 25(12): 1285-7, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27307448

ABSTRACT

Throughout the 20th century, a remarkable improvement in the prognosis of systemic lupus erythematosus (SLE) has been seen, mostly due to a better understanding of the disease and the advent of new therapies. However, a plateau seems to have been reached. Whilst outcomes related to active disease have greatly improved, damage accrual tends to be slowly increasing especially damage secondary to high-dose glucocorticoids, which could lead not only to increased morbidity but also to a worse long-term prognosis. Cardiovascular disease and infections still account for the majority of deaths yet both could potentially be improved, again, by the use of high-dose glucocorticoids. In addition, antimalarials have also demonstrated many beneficial effects on patients with lupus. Thus, the universal use of hydroxychloroquine, a more rational prescription of glucocorticoids and preventive strategies for cardiovascular disease can be used as measures with major impacts on the future prognosis of patients with SLE.


Subject(s)
Lupus Erythematosus, Systemic/diagnostic imaging , Humans , Immunosuppressive Agents/adverse effects , Immunosuppressive Agents/therapeutic use , Lupus Erythematosus, Systemic/drug therapy , Prognosis , Survival Analysis , Treatment Outcome
8.
Clin Epigenetics ; 7: 108, 2015.
Article in English | MEDLINE | ID: mdl-26457123

ABSTRACT

BACKGROUND: Given the implication of histone acetylation in memory processes, histone deacetylase inhibitors (HDACIs) have been postulated as potential modulators of cognitive impairment in Alzheimer's disease (AD). However, dose-dependent side effects have been described in patients with the currently available broad-spectrum HDACIs, explaining why their therapeutic potential has not been realized for chronic diseases. Here, by simultaneously targeting two independent enzyme activities, histone deacetylase (HDAC) and phosphodiesterase-5 (PDE5), we propose a novel mode of inhibitory action that might increase the therapeutic specificity of HDACIs. RESULTS: The combination of vorinostat, a pan-HDACI, and tadalafil, a PDE5 inhibitor, rescued the long-term potentiation impaired in slices from APP/PS1 mice. When administered in vivo, the combination of these drugs alleviated the cognitive deficits in AD mice, as well as the amyloid and tau pathology, and it reversed the reduced dendritic spine density on hippocampal neurons. Significantly, the combination of vorinostat and tadalafil was more effective than each drug alone, both against the symptoms and in terms of disease modification, and importantly, these effects persisted after a 4-week washout period. CONCLUSIONS: The results highlight the pharmacological potential of a combination of molecules that inhibit HDAC and PDE5 as a therapeutic approach for AD treatment.

9.
Pharmacol Biochem Behav ; 134: 6-11, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25931266

ABSTRACT

Central administration of oxytocin has been shown to induce yawning, penile erection, grooming and scratching. Yawning and penile erections are due to activation of oxytocinergic neurons in the paraventricular nucleus of the hypothalamus. We selectively bred two sublines from Sprague-Dawley rats, one with a high-yawning frequency (HY) of 20yawns/h, and one with a low-yawning (LY) frequency of 2yawns/h. The aim of the current study was to analyze the behavioral effects of centrally-administered oxytocin [15ng-10µg; intracerebroventricularly (i.c.v.)] on yawning, penile erections, grooming and scratching in adult male rats from both sublines. Oxytocin produced a dose-dependent increase in yawning and penile erection frequencies and this effect was significantly higher in the HY, compared to the LY, subline. However, the number of oxytocin-induced scratching bouts was significantly higher in the LY, compared to the HY group. In conclusion, these sublines represent a suitable model for detailed analysis of behavior induced by oxytocin and other neuropeptides in animals with different spontaneous expression of behavioral traits.


Subject(s)
Grooming/drug effects , Oxytocin/administration & dosage , Penile Erection/drug effects , Yawning/drug effects , Animals , Dose-Response Relationship, Drug , Injections, Intraventricular , Male , Oxytocin/pharmacology , Rats , Rats, Sprague-Dawley
10.
Lupus ; 23(3): 323-6, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24531426

ABSTRACT

Both acute pancreatitis and diffuse alveolar haemorrhage are rare conditions associated with systemic lupus erythematosus (SLE). In this case report, a 23-year-old female with SLE was diagnosed with lupus-associated pancreatitis and, within a few days and despite initial therapy with pulse methyl-prednisolone, subsequently suffered an acute respiratory failure due to a diffuse alveolar haemorrhage. The patient was admitted to the intensive care unit and treatment was intensified with cyclophosphamide and rituximab, which shortly induced the complete remission of SLE with resolution of both clinical conditions. She completed treatment with six pulses of cyclophosphamide followed by azathioprine, hydroxychloroquine and prednisone at initial doses of 20 mg/d with rapid tapering to 5 mg/d, without relapse of the disease during the following year. This case can illustrate that, even in severe, life-threatening SLE flares, it is possible to avoid high-dose prednisone, which has been associated with severe side effects, including infections. Acute pancreatitis and diffuse alveolar haemorrhage are rare conditions caused by SLE. DAH can be a life-threatening complication, with an early mortality of at least 50%. When facing such severe SLE activity, there is a general tendency to use high doses of prednisone as the initial therapy, maintaining such high doses for long periods of time, even after the clinical situation has subsided. We report a case of a young woman with SLE, suffering from acute pancreatitis and diffuse alveolar haemorrhage, who was successfully treated with pulse methyl-prednisolone, hydroxychloroquine, cyclophosphamide and rituximab, combined with medium doses of prednisone.


Subject(s)
Antibodies, Monoclonal, Murine-Derived/administration & dosage , Cyclophosphamide/administration & dosage , Immunosuppressive Agents/administration & dosage , Lupus Erythematosus, Systemic/drug therapy , Pancreatitis/drug therapy , Prednisone/administration & dosage , Respiratory Insufficiency/drug therapy , Acute Disease , Adult , Antibodies, Monoclonal, Murine-Derived/adverse effects , Cyclophosphamide/adverse effects , Disease Progression , Drug Therapy, Combination , Female , Hemorrhage/immunology , Humans , Immunosuppressive Agents/adverse effects , Lupus Erythematosus, Systemic/complications , Lupus Erythematosus, Systemic/diagnosis , Lupus Erythematosus, Systemic/immunology , Pancreatitis/immunology , Prednisone/adverse effects , Remission Induction , Respiratory Insufficiency/immunology , Rituximab , Severity of Illness Index , Tomography, X-Ray Computed , Treatment Outcome
11.
Rev. clín. esp. (Ed. impr.) ; 212(10): 491-498, nov. 2012. tab, ilus
Article in Spanish | IBECS | ID: ibc-107477

ABSTRACT

Las pacientes con lupus eritematoso sistémico están expuestas a un número no despreciable de potenciales complicaciones materno-fetales durante la gestación. El conocimiento de la influencia recíproca entre el lupus y el embarazo es un importante punto de partida para asegurar la correcta monitorización de las pacientes, así como lo es la realización de una exhaustiva valoración preconcepcional con el fin de evaluar de forma individualizada el riesgo de cada paciente. El perfil inmunológico, los antecedentes de nefropatía, la historia obstétrica previa, el daño crónico y la actividad son puntos clave que condicionarán el perfil de riesgo. Por último, es fundamental asegurar un correcto manejo farmacológico en este período, teniendo en cuenta el perfil de seguridad de los diversos tratamientos durante el embarazo y la lactancia(AU)


Patients with systemic lupus eythematosus are exposed to a remarkably high number of maternal-fetal complications during pregnancy. Knowledge regarding the reciprocal influence between lupus and pregnancy is the starting point to assure that these patients are correctly monitored. It is also important to carry out comprehensive preconception evaluation to individually evaluate the risk of each patient. The immunological profile, history of nephritis, presence of chronic damage and disease activity are the basic data that will determine the specific individual risk profile. Finally, correct drug management must be assured during this period, based on the safety profile of the different treatments during pregnancy and lactation(AU)


Subject(s)
Humans , Female , Pregnancy , Adult , Pregnancy Complications, Hematologic/diagnosis , Pregnancy Complications, Hematologic/surgery , Lupus Erythematosus, Systemic/complications , Prednisone/therapeutic use , Antiphospholipid Syndrome/complications , Proteinuria/complications , Proteinuria/diagnosis , Lupus Nephritis/complications , Lupus Nephritis/diagnosis , Lupus Erythematosus, Systemic/drug therapy , Lupus Erythematosus, Systemic/physiopathology , Biopsy/methods , Biopsy , Lupus Nephritis/physiopathology , Breast Feeding/methods , Breast Feeding/trends , Antibiotic Prophylaxis/methods , Post-Exposure Prophylaxis/methods
12.
Acta Psychiatr Scand ; 125(4): 335-41, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22283440

ABSTRACT

OBJECTIVE: The aim of this 1-year follow-up study was to compare functional outcome as well as clinical differences between patients with first- and multiple-episode bipolar disorder. METHOD: Bipolar disorder patients with first (n = 60) and multiple episodes (n = 59) were recruited from two hospitals in Spain. The Functioning Assessment Short Test (FAST) was used to assess functioning. The Hamilton Depression Rating Scale (HAMD) and the Young Mania Rating Scale (YMRS) were administered to assess mood symptoms. RESULTS: As expected, patients with first episode experienced a greater functioning compared to patients with multiple episodes (11.26 ± 10.94 vs. 26.91 ± 13.96; t = 6.436, P < 0.001). There were significant demographic and clinical differences between both groups. Baseline depressive symptoms (F = 9.553, df = 4, 102; P < 0.001) and age (F = 14.145, df = 4, 103; P < 0.001) were significantly associated with poor functional recovery at 6-month and 12-month assessment, respectively, in a group of patients with multiple episodes. CONCLUSION: Our data give support to the model of staging in bipolar disorder, showing that the enduring neurotoxicity of repeated episodes may contribute to sustained impairment in multiple areas of psychosocial functioning.


Subject(s)
Activities of Daily Living/psychology , Bipolar Disorder/physiopathology , Bipolar Disorder/psychology , Cognition , Employment/psychology , Interpersonal Relations , Adult , Disease Progression , Female , Follow-Up Studies , Humans , Leisure Activities/psychology , Male , Middle Aged , Recovery of Function
13.
Rev Clin Esp ; 212(10): 491-8, 2012 Nov.
Article in Spanish | MEDLINE | ID: mdl-22245369

ABSTRACT

Patients with systemic lupus erythematosus are exposed to a remarkably high number of maternal-fetal complications during pregnancy. Knowledge regarding the reciprocal influence between lupus and pregnancy is the starting point to assure that these patients are correctly monitored. It is also important to carry out comprehensive preconception evaluation to individually evaluate the risk of each patient. The immunological profile, history of nephritis, presence of chronic damage and disease activity are the basic data that will determine the specific individual risk profile. Finally, correct drug management must be assured during this period, based on the safety profile of the different treatments during pregnancy and lactation.


Subject(s)
Anti-Inflammatory Agents/therapeutic use , Immunosuppressive Agents/therapeutic use , Lupus Erythematosus, Systemic/drug therapy , Postnatal Care/methods , Pregnancy Complications/drug therapy , Prenatal Care/methods , Adult , Breast Feeding , Female , Humans , Pregnancy , Pregnancy Complications/etiology , Pregnancy Complications/prevention & control
14.
Rev. Asoc. Esp. Espec. Med. Trab ; 20(1): 14-20, abr. 2011. tab
Article in Spanish | IBECS | ID: ibc-91829

ABSTRACT

Como resultado de la vigilancia de la salud, el servicio médico realiza un análisis del trabajador y del puesto a ocupar, emitiendo el certificado de aptitud, que puede contemplar restricciones para determinados puestos. Este proceso conlleva una decisión que en los casos más complicados suele generar dudas en su análisis y conclusiones diferentes entre diferentes médicos e incluso en el mismo profesional. Se presenta una herramienta y una sistemática de actuación que permite valorar el nivel de riesgo personal para cada trabajador y puesto de trabajo, aportando a su vez criterios objetivos que reducen la variabilidad intra- e interobservador, facilitando el análisis, tanto de la decisión sobre la aptitud del trabajador, como en la evaluación y propuestas de mejora (AU)


As a result of the health surveillance, the medical service conducts an analysis of the worker and workers places, issuing the certificate for work, which can have restrictions for work in particular work places. This process involves a decision that the more complicated cases often create doubts in its analysis and conclusions differ among different doctors and even in the same professional. Is a tool and systematic action that allows assess the level of personal risk to each worker and job. This article shows a tool and systematicall behaviour which can evaluate the personal risk value in each worker and work places. Contributing to turn objective criteria that reduce the variability intraand interobserver, making easier analysis and both of the decision on the suitability of the worker, as in the assessment and proposals of the improvements (AU)


Subject(s)
Humans , Occupational Risks , Risk Reduction Behavior , Surveillance of the Workers Health , Safety Management , Aptitude , Accident Prevention/methods
15.
Pediatr. aten. prim ; 12(47): 399-411, jul.-sept. 2010. tab
Article in Spanish | IBECS | ID: ibc-82160

ABSTRACT

Introducción: la inmigración ha hecho aumentar la prevalencia de la infección tuberculosa latente, por tanto es interesante conocer los resultados de la Prueba de Tuberculina (PT) en la población infantil inmigrada. Pacientes y método: Estudio multicéntrico, transversal y descriptivo. Se realizó la PT a niños de 6 meses a 15 años de Países de Baja Renta (PBR) que hacia menos de 12 meses que habían inmigrado. Se estudió algunos factores relacionados con el resultado de la PT y el cumplimiento de su lectura. Resultados: De 1009 niños, presentaron una PT positiva el 6,1% (Intervalo de confianza 95%: 4,7-7,7). El 83% con cicatriz de BCG tenían 0mm de induración. Hubo mayor prevalencia de PT positiva entre los vacunados BCG hacía más de 3 años. La PT positiva aumentaba con la edad. No hubo asociación significativa entre la PT positiva y el sexo, nivel cultural de los padres ni hacinamiento en nuestro país. Todos los niños con contacto con bacilífero tuvieron la PT positiva. No se leyó la PT en el 3,7%, lo que se asoció con el índice de hacinamiento >2 y con que el padre no trabajase. No se observó diferencia estadísticamente significativa entre la negatividad de la PT y la presencia o no de parasitación intestinal. Conclusiones: Consideramos indicada la realización de la PT a niños inmigrados de PBR(AU)


Subject(s)
Humans , Male , Female , Child, Preschool , Child , Emigrants and Immigrants/statistics & numerical data , Tuberculin/administration & dosage , Tuberculin , Tuberculin Test/methods , Tuberculin Test/statistics & numerical data , Tuberculosis/epidemiology , Tuberculosis/immunology , Vaccination/statistics & numerical data , Cross-Sectional Studies , Confidence Intervals , Vaccination/methods , Vaccination/trends , Signs and Symptoms , Radiography, Thoracic , Primary Health Care/methods
16.
Ann Rheum Dis ; 66(6): 815-7, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17204564

ABSTRACT

BACKGROUND: Recent studies suggest that antimalarials have antineoplastic properties. OBJECTIVE: To investigate whether antimalarials decrease the risk of cancer in systemic lupus erythematosus (SLE). METHODS: An observational prospective cohort study was carried out. 235 patients were included in the study at the time of diagnosis (American College of Rheumatology criteria). The end point was the diagnosis of cancer. Kaplan-Meier cancer-free survival curves for patients treated and not treated with antimalarials were compared. A Cox proportional hazards model was fitted, with cancer as the dependent variable. Age at diagnosis, gender, treatment with azathioprine, cyclophosphamide and methotrexate, smoking, Systemic Lupus International Collaborating Clinics (SLICC) Damage Index 6 months after diagnosis, year of diagnosis and treatment with antimalarials were entered as independent variables. RESULTS: 209 (89%) patients were women. 233 (99%) patients were white. Mean (SD) age at diagnosis was 37 (16) years. Median (range) follow-up was 10 (1-31) years. 156 (66%) patients had ever received antimalarials. 2/156 (1.3%) ever-treated patients compared with 11/79 (13%) never-treated patients had cancer (p<0.001). Cumulative cancer-free survival in treated and not treated patients was 0.98 and 0.73, respectively (p<0.001). Adjusted hazard ratio for cancer among malaria drug users compared with non-users was 0.15 (95% CI 0.02 to 0.99). CONCLUSIONS: This study launches the hypothesis of a protective action of antimalarials against cancer in patients with SLE. This effect should be confirmed in larger multicentre studies.


Subject(s)
Antimalarials/therapeutic use , Antineoplastic Agents/therapeutic use , Lupus Erythematosus, Systemic/drug therapy , Neoplasms/prevention & control , Adolescent , Adult , Antirheumatic Agents/therapeutic use , Drug Therapy, Combination , Epidemiologic Methods , Female , Humans , Immunosuppressive Agents/therapeutic use , Male , Middle Aged
SELECTION OF CITATIONS
SEARCH DETAIL