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1.
Rev Gastroenterol Mex (Engl Ed) ; 88(2): 125-131, 2023.
Article in English | MEDLINE | ID: mdl-35523683

ABSTRACT

INTRODUCTION AND AIMS: Celiac disease (CD) is a complex condition, whose main genetic determinant involves HLA molecules, specifically the HLA-DQ2 and/or HLA-DQ8 heterodimers. Nevertheless, the frequency of the alleles encoding those molecules has not been reported in Venezuelan celiac patients. Therefore, the aim of our study was to evaluate the frequency of the HLA-DQB1 alleles in individuals with symptoms suggestive of CD and define the diagnostic markers of the condition in a Venezuelan population. MATERIAL AND METHODS: A cross-sectional study included 516 individuals with symptoms suggestive of CD. Molecular typing of the HLA-DQB1 locus was performed using a polymerase chain reaction-sequence-specific oligonucleotide procedure (PCR-SSO). RESULTS: A total of 58.3% of the individuals with clinical manifestations consistent with CD presented with at least one risk allele (DQB1*0201 and/or DQB1*0302), and the diagnosis was confirmed in 40 of them. The patients with CD had a higher frequency of the DQB1*0201 risk allele (26.25%), followed by the DQB1*0302 (17.5%) allele. There was an association between the presence of risk alleles and the presence of lesions characteristic of CD (P = 0.001), and a correlation was found between the genetic predisposition to develop CD and the presence of anti-tissue transglutaminase antibodies (P = 0.0127). CONCLUSIONS: The results support the role of the DQB1*02 and DQB1*0302 alleles in CD susceptibility and the histologic alterations of the intestinal mucosa, in a Venezuelan population.


Subject(s)
Celiac Disease , Humans , Alleles , Celiac Disease/diagnosis , Celiac Disease/genetics , Cross-Sectional Studies , HLA-DQ beta-Chains/genetics
2.
Haemophilia ; 24(4): e179-e186, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29855125

ABSTRACT

INTRODUCTION: Jamaica has an estimated 200 persons with haemophilia (PWH), who face significant constraints in access to specialized haemophilia care, including access to clotting factor concentrates. AIM: The aim of this paper is to establish the current burden of disease in PWH in Jamaica. METHODS: PWH were enrolled through the University Hospital of the West Indies, Jamaica. The impact of haemophilia was assessed using a comprehensive battery of heath outcome measures that included the following: laboratory, clinical information and validated outcome measures of joint structure and function, activity, and health-related quality of life (HRQoL) to provide a health profile of the Jamaican haemophilia population. RESULTS: In all, 45 PWH were registered (mean age: 29, range: 0.17-69 years), including 13 children (<18 years of age) and 32 adults. In this sample, 41 had haemophilia A (30 severe) and 4 had haemophilia B (3 severe); 10 patients with haemophilia A were inhibitor positive. The results indicate that adults with haemophilia in Jamaica have significant joint damage: mean Haemophilia Joint Health Score (HJHS) = 42.1 (SD = 17.3); moderate activity levels - mean Haemophilia Activities List (HAL) score = 64.8 (SD = 17.8); and low HRQoL scores - mean Haemo-QoL-A score = 62.3 (SD = 19.4). Results for children are also reported but should be interpreted with caution due to the small sample size. CONCLUSIONS: There is a very high burden of disease in PWH in Jamaica. The health profiles reported in this paper are an essential first step in advocating for a multidisciplinary Comprehensive Care Program for assessment and care of PWH in Jamaica.


Subject(s)
Cost of Illness , Hemophilia A/economics , Hemophilia A/epidemiology , Hemophilia B/economics , Hemophilia B/epidemiology , Registries , Adolescent , Adult , Aged , Child , Child, Preschool , Female , Humans , Infant , Jamaica/epidemiology , Male , Middle Aged , Quality of Life , Surveys and Questionnaires , Young Adult
3.
West Indian med. j ; West Indian med. j;62(7): 575-581, Sept. 2013. graf, tab
Article in English | LILACS | ID: biblio-1045707

ABSTRACT

OBJECTIVES: There have been several modifications to the classification of childhood cancers since the first report (1968-1981) specific to the Jamaican paediatric population was published in 1988. This paper reports on paediatric cancer incidence in Kingston and St Andrew, Jamaica, for the 20-year period 1983-2002 based on these modifications. METHODS: All cases of cancer diagnosed in children (0-14 years), between 1983 and 2002 were extracted from the Jamaica Cancer Registry archives and classified using the International Classification of Childhood Cancer, third edition. Incidence figures were calculated as per the International Agency for Research on Cancer (IARC) reporting format for childhood cancer. RESULTS: There were 272 cases (133 males, 139 females) of childhood cancer identified in the 20-year period. The overall age standardized rate (ASR) was 69.4 per million; that for males was 67.8 per million, and for females, 70.9 per million. The three most common malignancies overall were leukaemia (21.3%), lymphoma (15.8%) and brain and spinal neoplasms (14.0%). In males, the highest ASRs were seen for leukaemia (14.8 per million), lymphoma (12.7 per million), and brain and spinal neoplasms (8.2 per million), and in females, leukaemia (14.4 per million), nephroblastoma (11.3 per million), and brain and spinal neoplasms (10.6 per million). CONCLUSIONS: The rankings of the most common childhood malignancies in Jamaica (leukaemia, brain and spinal neoplasms and lymphomas) have shown few changes since the last review. However, there are differences in frequency and gender distribution of nephroblastoma and brain and spinal neoplasms.


OBJETIVOS: Ha habido varias modificaciones a la clasificación de los cánceres infantiles desde que el primer informe (1968-1981) específico para la población pediátrica jamaicana fue publicado en 1988. Este artículo reporta la incidencia de cáncer pediátrico en Kingston y Saint Andrew, Jamaica, en el período de 20 años de1983-2002, basado en estas modificaciones. MÉTODOS: Todos los casos de cáncer diagnosticados en niños (0-14 años) entre 1983 y 2002 fueron extraídos de los archivos del Registro de Cáncer en Jamaica, y clasificados utilizando la tercera edición de la Clasificación Internacional del Cáncer Infantil. Las cifras de incidencia fueron calculas siguiendo el formato de reporte de cáncer infantil de la Agencia Internacional para la Investigación del Cáncer (IARC, siglas en inglés). RESULTADOS: Hubo 272 casos de cáncer infantil (133 varones y 139 hembras) identificados en el período de 20 años. La tasa general de incidencia estandarizada por edad (ASR. siglas en inglés) fue 69.4 por millón; para los varones fue 67.8 por millón, y para las hembras, 70.9 por millón. En general, los tres tumores malignos más comunes fueron la leucemia (21.3%), el linfoma (15.8%) y las neoplasias del cerebro y la médula espinal (14.0%). En los varones, las tasas de ASR más altas fueron las observadas en relación con la leucemia (14.8 por millón), los linfomas (12.7 por millón), y las neoplasias del cerebro y la médula (8.2 por millón); en las hembras, la leucemia (14.4 por millón), los nefroblastomas (11.3por millón), y las neoplasias de cerebro y médula (10.6por millón). CONCLUSIÓN: Las clasificaciones por nivel de incidencia de los tumores malignos infantiles más comúnes en Jamaica (la leucemia, las neoplasias del cerebro y la médula espinal, y los linfomas) han mostrado pocos cambios desde la última revisión. Sin embargo, existen diferencias en la frecuencia así como en la distribución por sexo con respecto a los nefroblastomas y las neoplasias del cerebro y la médula.


Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Child , Adolescent , Neoplasms/epidemiology , Spinal Neoplasms/epidemiology , Urban Population/statistics & numerical data , Brain Neoplasms/epidemiology , Leukemia/epidemiology , Incidence , Wilms Tumor/epidemiology , Jamaica/epidemiology , Kidney Neoplasms/epidemiology , Lymphoma/epidemiology
4.
West Indian Med J ; 62(7): 575-81, 2013 Sep.
Article in English | MEDLINE | ID: mdl-24831892

ABSTRACT

OBJECTIVES: There have been several modifications to the classification of childhood cancers since the first report (1968-1981) specific to the Jamaican paediatric population was published in 1988. This paper reports on paediatric cancer incidence in Kingston and St Andrew, Jamaica, for the 20-year period 1983-2002 based on these modifications. METHODS: All cases of cancer diagnosed in children (0-14 years), between 1983 and 2002 were extracted from the Jamaica Cancer Registry archives and classified using the International Classification of Childhood Cancer, third edition. Incidence figures were calculated as per the International Agency for Research on Cancer (IARC) reporting format for childhood cancer. RESULTS: There were 272 cases (133 males, 139 females) of childhood cancer identified in the 20-year period. The overall age standardized rate (ASR) was 69.4 per million; that for males was 67.8 per million, and for females, 70.9 per million. The three most common malignancies overall were leukaemia (21.3%), lymphoma (15.8%) and brain and spinal neoplasms (14.0%). In males, the highest ASRs were seen for leukaemia (14.8 per million), lymphoma (12.7 per million), and brain and spinal neoplasms (8.2 per million), and in females, leukaemia (14.4 per million), nephroblastoma (11.3 per million), and brain and spinal neoplasms (10.6 per million). CONCLUSIONS: The rankings of the most common childhood malignancies in Jamaica (leukaemia, brain and spinal neoplasms and lymphomas) have shown few changes since the last review. However, there are differences in frequency and gender distribution of nephroblastoma and brain and spinal neoplasms.


Subject(s)
Neoplasms/epidemiology , Adolescent , Brain Neoplasms/epidemiology , Child , Child, Preschool , Female , Humans , Incidence , Infant , Jamaica/epidemiology , Kidney Neoplasms/epidemiology , Leukemia/epidemiology , Lymphoma/epidemiology , Male , Spinal Neoplasms/epidemiology , Urban Population/statistics & numerical data , Wilms Tumor/epidemiology
5.
Fitoterapia ; 81(8): 1113-6, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20627119

ABSTRACT

We investigated the in vitro effect of dibenzyl trisulfide (DTS), a secondary metabolite of Petiveria alliacea, on erythrocyte elasticity, relaxation time and membrane morphology. Blood samples from 8 volunteers with hemoglobin AA were exposed to 100, 200, 400, 800 and 1000 ng/ml of DTS respectively and the elasticity and relaxation time measured. There were statistically significant, dose-dependent increases in elasticity and relaxation times. The changes in membrane morphology observed also increased with increased concentration of DTS. This suggests that DTS interaction with membrane protein resulted in increased elasticity, relaxation time and deformation of the erythrocyte membrane.


Subject(s)
Benzyl Compounds/chemistry , Benzyl Compounds/pharmacology , Erythrocyte Membrane/drug effects , Phytolaccaceae/chemistry , Phytolaccaceae/metabolism , Sulfides/chemistry , Sulfides/pharmacology , Female , Humans , Male , Molecular Structure
6.
Int. j. tuberc. lung. dis ; 11(9): 1026-1032, Sep 2007. tabgraf
Article in English | MedCarib | ID: med-17744

ABSTRACT

SETTING: Underdiagnosis of chronic obstructive pulmonary disease (COPD) in asthmatics attending specialty care in Trinidad, West Indies. OBJECTIVE: To determine the prevalence of COPD in diagnosed asthmatics receiving specialty respiratory care. DESIGN: In a cross-sectional study, 258 asthmatics were screened for lung function measures to examine forced expiratory volume after 1 second (FEV1), forced vital capacity (FVC) and post-bronchodilator FEV1/FVC (COPD was defined as FEV1/FVC < 70 per cent). RESULTS: Of 165 patients evaluated (response rate 64.0 per cent), 53 (32.1 per cent, 95 per centCI 25.0-39.2) had a study diagnosis of COPD and a mean FEV1/FVC of 60.12 +/- 1.2. Proportionally, more males had COPD (50.9 per cent) than asthma (24.1 per cent, P < 0.001). Patients with COPD were 10 years older than asthmatics (P < 0.001). Persons with asthma who smoked were more likely to have COPD (56.0 per cent) (OR 3.26, 95 per cent CI 1.36-7.80, P = 0.006). In both sexes, FEV1/FVC was lower among older people (P < 0.001), with a greater effect (OR 2.75, 95 per cent CI 1.00-7.56, P < 0.01) seen among men in this cross-sectional study. CONCLUSIONS: One third of diagnosed asthmatics in specialty care also have COPD. Lung function was lower among older persons. Early spirometric evaluation of elderly asthmatics who smoke can determine the presence of COPD and facilitate appropriate management.


Subject(s)
Humans , Pulmonary Disease, Chronic Obstructive , Asthma , Trinidad and Tobago
7.
Int J Tuberc Lung Dis ; 11(9): 1026-32, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17705983

ABSTRACT

SETTING: Underdiagnosis of chronic obstructive pulmonary disease (COPD) in asthmatics attending specialty care in Trinidad, West Indies. OBJECTIVE: To determine the prevalence of COPD in diagnosed asthmatics receiving specialty respiratory care. DESIGN: In a cross-sectional study, 258 asthmatics were screened for lung function measures to examine forced expiratory volume after 1 second (FEV1), forced vital capacity (FVC) and post-bronchodilator FEV1/FVC (COPD was defined as FEV1/FVC < 70%). RESULTS: Of 165 patients evaluated (response rate 64.0%), 53 (32.1%, 95%CI 25.0-39.2) had a study diagnosis of COPD and a mean FEV1/FVC of 60.12 +/- 1.2. Proportionally, more males had COPD (50.9%) than asthma (24.1%, P < 0.001). Patients with COPD were 10 years older than asthmatics (P < 0.001). Persons with asthma who smoked were more likely to have COPD (56.0%) (OR 3.26, 95%CI 1.36-7.80, P = 0.006). In both sexes, FEV1/FVC was lower among older people (P < 0.001), with a greater effect (OR 2.75, 95%CI 1.00-7.56, P < 0.01) seen among men in this cross-sectional study. CONCLUSIONS: One third of diagnosed asthmatics in specialty care also have COPD. Lung function was lower among older persons. Early spirometric evaluation of elderly asthmatics who smoke can determine the presence of COPD and facilitate appropriate management.


Subject(s)
Asthma/complications , Pulmonary Disease, Chronic Obstructive/diagnosis , Pulmonary Disease, Chronic Obstructive/epidemiology , Adolescent , Adult , Aged , Aged, 80 and over , Asthma/epidemiology , Cross-Sectional Studies , Diagnostic Errors , Female , Humans , Linear Models , Male , Middle Aged , Prevalence , Pulmonary Disease, Chronic Obstructive/complications , Respiratory Function Tests , Risk Factors , Smoking/adverse effects , Trinidad and Tobago/epidemiology
8.
J Nutr ; 130(8S Suppl): 2057S-72S, 2000 08.
Article in English | MEDLINE | ID: mdl-10917925

ABSTRACT

The medicinal use of cacao, or chocolate, both as a primary remedy and as a vehicle to deliver other medicines, originated in the New World and diffused to Europe in the mid 1500s. These practices originated among the Olmec, Maya and Mexica (Aztec). The word cacao is derived from Olmec and the subsequent Mayan languages (kakaw); the chocolate-related term cacahuatl is Nahuatl (Aztec language), derived from Olmec/Mayan etymology. Early colonial era documents included instructions for the medicinal use of cacao. The Badianus Codex (1552) noted the use of cacao flowers to treat fatigue, whereas the Florentine Codex (1590) offered a prescription of cacao beans, maize and the herb tlacoxochitl (Calliandra anomala) to alleviate fever and panting of breath and to treat the faint of heart. Subsequent 16th to early 20th century manuscripts produced in Europe and New Spain revealed >100 medicinal uses for cacao/chocolate. Three consistent roles can be identified: 1) to treat emaciated patients to gain weight; 2) to stimulate nervous systems of apathetic, exhausted or feeble patients; and 3) to improve digestion and elimination where cacao/chocolate countered the effects of stagnant or weak stomachs, stimulated kidneys and improved bowel function. Additional medical complaints treated with chocolate/cacao have included anemia, poor appetite, mental fatigue, poor breast milk production, consumption/tuberculosis, fever, gout, kidney stones, reduced longevity and poor sexual appetite/low virility. Chocolate paste was a medium used to administer drugs and to counter the taste of bitter pharmacological additives. In addition to cacao beans, preparations of cacao bark, oil (cacao butter), leaves and flowers have been used to treat burns, bowel dysfunction, cuts and skin irritations.


Subject(s)
Cacao/history , Cacao/therapeutic use , Central America , Europe , Female , History, 16th Century , History, 17th Century , History, 18th Century , History, 19th Century , History, 20th Century , Humans , Male , Phytotherapy
9.
London; Wolfe Medical; 1990. 144 p. ilus, tab, graf, 27cm.
Monography in English | LILACS, HANSEN, Hanseníase Leprosy, SESSP-ILSLACERVO, Sec. Est. Saúde SP | ID: biblio-1084966
10.
Cytogenet Cell Genet ; 52(1-2): 19-22, 1989.
Article in English | MEDLINE | ID: mdl-2558855

ABSTRACT

The human gene encoding differentiation-stimulating factor (D-factor) has previously been isolated and shown to be identical to leukemia inhibitory factor (LIF). We have determined a fine structure map of approximately 20-kb surrounding the D-factor/LIF gene. Southern blot analysis using a somatic cell hybrid panel shows that the gene maps to chromosome 22. D-factor/LIF was further sublocalized to 22q11.2----q13.1, distal to a Ewing sarcoma (ES) breakpoint, using a second somatic cell hybrid panel. Probes to the 5' and 3' regions of the locus and the cDNA were used to screen for restriction fragment length polymorphisms, but none were detected. Analysis by pulsed field gel electrophoresis suggests that D-factor/LIF is not near the ES breakpoint.


Subject(s)
Chromosomes, Human, Pair 22 , Growth Inhibitors/genetics , Interleukin-6 , Lymphokines , Sarcoma, Ewing/genetics , Animals , Blotting, Southern , Chromosome Aberrations , Chromosome Disorders , Chromosome Mapping , DNA Probes , DNA Restriction Enzymes , Electrophoresis, Agar Gel , Genetic Linkage , Humans , Hybrid Cells , Leukemia Inhibitory Factor
11.
Science ; 233(4767): 964-7, 1986 Aug 29.
Article in English | MEDLINE | ID: mdl-17732039

ABSTRACT

The 13 November 1985 eruption of Nevado del Ruiz volcano, in Colombia, released a small volume of pyroclastic material and a disproportionately large volume of volcanic gas. Before the eruption, summit fumarole gases became less water-rich, and the sulfur/chlorine ratio increased. Remote measurements of sulfur dioxide flux after the eruption indicated active degassing at levels associated with eruptive or inter-eruptive stages of other volcanoes. Thermal water analyses revealed increases in magnesium, calcium, and potassium and an increase in the magnesium/chlorine ratio, suggesting that these elements may have been leached from new magma. Ash leachate data showed sulfate and chloride concentrations and ratios that would be expected for the late stages ofa major Plinian eruption. Water from the lahar contained high concentrations of sulfate and had a sulfur/chlorine ratio of 4.67, suggesting that water ejected from the crater lake and turbulent mixing of pyroclasts and glacial ice triggered the lahar. Microprobe analyses of pumice from this eruption and the most recent previous event showed similar mixed andesites. The uniform composition of the pumices and the unusually high ratio of gas to magma suggest that, although a new batch of magma triggered this eruption, the pumice that erupted may actually be old. Large volumes of new magma and glacial ice make the volcano dangerous and should stimulate development of an integrated long-term monitoring program to include Tolima volcano, 25 kilometers to the south.

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