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1.
JCO Oncol Pract ; 16(11): e1332-e1342, 2020 11.
Artículo en Inglés | MEDLINE | ID: mdl-32603251

RESUMEN

PURPOSE: Little information exists on factors that predict opioid misuse in oncology. We adopted the Screener and Opioid Assessment for Patients With Pain-Short Form (SOAPP-SF) and toxicology testing to assess for opioid misuse risk. The primary objective was to (1) identify characteristics associated with a high-risk SOAPP-SF score and noncompliant toxicology test, and (2) determine SOAPP-SF utility to predict noncompliant toxicology tests. METHODS: From July 1, 2017, to December 31, 2017, new patients completed the Edmonton Symptom Assessment Scale (ESAS), SOAPP-SF, and narcotic use agreement. Toxicology test results were collected at subsequent visits. RESULTS: Of 223 distinct patients, 96% completed SOAPP-SF. Mean age was 61 ± 12.7 years, 58% were female, 68% were White, and 28% were Black. Eighty-three eligible patients (38%) completed toxicology testing. Younger age, male sex, and increased ESAS depression scores were associated with high-risk SOAPP-SF scores. Smoking habit was associated with an aberrant test. An SOAPP-SF score ≥ 3 predicted a noncompliant toxicology test. CONCLUSION: Male sex, young age, and higher ESAS depression score were associated with a high SOAPP-SF score. Smoking habit was associated with an aberrant test. An SOAPP-SF of ≥ 3 (sensitivity, 0.74; specificity, 0.64), not ≥ 4, was predictive of an aberrant test; however, performance characteristics were decreased from those published by Inflexxion, for ≥ 4 (sensitivity, 0.86; specificity, 0.67). The specificity warrants caution in falsely labeling patients. The SOAPP-SF may aid in meeting National Comprehensive Cancer Network recommendations to screen oncology patients for opioid misuse.


Asunto(s)
Trastornos Relacionados con Opioides , Medicina Paliativa , Anciano , Analgésicos Opioides/efectos adversos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Trastornos Relacionados con Opioides/tratamiento farmacológico , Trastornos Relacionados con Opioides/epidemiología , Dolor/tratamiento farmacológico , Medición de Riesgo
2.
Lipids ; 38(6): 683-6, 2003 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-12934680

RESUMEN

The effect of dietary n-3 FA deficiency on bone tissue FA composition was evaluated in growing rats. Two mixtures combining hydrogenated coconut oil with safflower oil served as the n-3-deficient dietary treatments and provided two levels of linoleic acid (LA). The n-3 treatments were formulated with added alpha-linolenic acid (LNA) from flaxseed oil (diet LNA) or LNA plus DHA, and both were balanced for LA. This study showed that bone is sensitive to changes in dietary n-3 FA and that DHA is more effective than LNA in maintaining DHA levels in these tissues.


Asunto(s)
Huesos/química , Ácidos Grasos Omega-3/administración & dosificación , Ácidos Grasos Omega-3/análisis , Ácidos Grasos/análisis , Animales , Médula Ósea/química , Médula Ósea/efectos de los fármacos , Huesos/efectos de los fármacos , Huesos/metabolismo , Ácidos Docosahexaenoicos/administración & dosificación , Ácidos Docosahexaenoicos/farmacología , Femenino , Fémur/química , Fémur/efectos de los fármacos , Aceite de Linaza/administración & dosificación , Aceite de Linaza/farmacología , Ratas , Ratas Long-Evans , Tibia/química , Tibia/efectos de los fármacos , Ácido alfa-Linolénico/administración & dosificación , Ácido alfa-Linolénico/farmacología
3.
Lipids ; 38(4): 431-5, 2003 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-12848290

RESUMEN

The reciprocal replacement of DHA by docosapentaenoic acid (DPAn-6) was studied in rats that consumed an n-3 FA-deficient or n-3 FA-adequate diet. Dams were fed the two experimental diets from weaning and throughout pregnancy and lactation. Their pups were then fed the respective diets after weaning. Cortex FA analysis was performed at various times (0, 5, 10, 20, 50, and 91 d) after birth to determine whether DPAn-6 completely replaced DHA in the n-3-deficient group. Cortical DHA levels were significantly lower (average 86%) in the n-3-deficient rats. DPAn-6 increased significantly in the n-3-deficient rats starting with a 6.5-fold increase at day 0 up to a 54-fold increase at day 91 compared with the n-3-adequate group. However, this significant increase did not completely replace the loss of DHA at postnatal days 5, 10, and 20 in which there was still an 11.5, 10.3, and 8.0% deficit in the sum of DHA and DPAn-6, respectively, in the n-3-deficient group. Once docosatetraenoic (DTA) and arachidonic acids (AA) were included in the sum (DHA + DPAn-6 + DTA + AA), the levels between the two groups were similar. These results suggest that not only DPAn-6 but also other n-6 FA, including DTA and AA, replace DHA in n-3-deficient rats. The lack of total 22-carbon (22C) FA in the brain during the rapid membrane biogenesis that occurs during early development could be a factor in the nervous system functional deficits associated with n-3 FA deficiency.


Asunto(s)
Fenómenos Fisiológicos Nutricionales de los Animales , Corteza Cerebral/crecimiento & desarrollo , Corteza Cerebral/metabolismo , Ácidos Docosahexaenoicos/metabolismo , Ácidos Grasos Omega-3/administración & dosificación , Ácidos Grasos Insaturados/metabolismo , Alimentación Animal , Animales , Ácido Araquidónico/análisis , Ácido Araquidónico/metabolismo , Corteza Cerebral/química , Ácidos Docosahexaenoicos/análisis , Ácidos Erucicos/análisis , Ácidos Erucicos/química , Ácidos Erucicos/metabolismo , Ácidos Grasos/análisis , Ácidos Grasos/química , Ácidos Grasos Omega-3/metabolismo , Ácidos Grasos Insaturados/análisis , Femenino , Masculino , Ratas , Ratas Long-Evans
4.
Behav Neurosci ; 116(6): 1022-31, 2002 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-12492301

RESUMEN

This study investigated the influence of brain docosahexaenoic acid (DHA) deficiency on simple and complex olfactory-based learning and memory in 2nd generation (F2) adult male rats. Rats raised and maintained on either an n-3-adequate or an n-3-deficient diet were tested for acquisition of an olfactory learning set and an olfactory memory task, and for motivation to obtain a water reward. Despite a 76% decrease in brain DHA, n-3-deficient rats were able to acquire most simple 2-odor discrimination tasks but were deficient in the acquisition of a 20-problem olfactory learning set. This deficit could not be attributed to changes in sensory capacity but, instead, appeared to represent a deficit in higher order learning.


Asunto(s)
Trastornos del Conocimiento/fisiopatología , Enfermedades Carenciales/complicaciones , Aprendizaje Discriminativo , Ácidos Docosahexaenoicos/farmacología , Trastornos de la Memoria/etiología , Animales , Química Encefálica , Enfermedades Carenciales/fisiopatología , Enfermedades Carenciales/veterinaria , Masculino , Ratas , Ratas Long-Evans , Olfato
5.
Nutr Neurosci ; 5(2): 103-13, 2002 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-12004794

RESUMEN

Rats raised on n-3 essential fatty acid deficient diets demonstrate spatial memory deficits. To investigate neuroanatomical correlates of these deficits, morphological analysis of the hippocampus were carried out. Adult, female rats were raised for three generations on n-3 deficient or n-3 supplemented diets. Two n-3 deficient diets contained adequate linoleic acid (LA), or high linoleic acid (high LA), and two supplemented diets contained LA supplemented with alpha-linolenic acid (+LNA), or linoleic supplementation with alpha-linolenic and docosahexaenoic acids (+LNA/DHA). The total fatty acid composition of the hippocampus revealed a profound loss (90%) in docosahexaenoic acid (DHA) in the hippocampi of LA and high LA animals compared to those on +LNA and +LNA/DHA diets with a reciprocal increase in docosapentaenoic acid (DPAn-6) in all phospholipid species. The volume, density, total number, and cell body size of neurons in CA1-3, granular and hilar layers of the hippocampus were measured at septal and temporal locations using unbiased stereology. No differences were detected in any of these measures except for in cell body size; CA1 pyramidal neurons in the LA group were significantly (p < 0.04) smaller than neurons in the +LNA/DHA group at the septal location.


Asunto(s)
Tamaño de la Célula , Ácidos Docosahexaenoicos/análisis , Hipocampo/química , Hipocampo/citología , Animales , Recuento de Células , Grasas de la Dieta/administración & dosificación , Ácidos Docosahexaenoicos/administración & dosificación , Ácidos Grasos/análisis , Ácidos Grasos Omega-3/administración & dosificación , Femenino , Ácido Linoleico/administración & dosificación , Neuronas/citología , Ratas , Ratas Long-Evans , Ácido alfa-Linolénico/administración & dosificación
6.
Lipids ; 37(4): 367-74, 2002 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-12030317

RESUMEN

Peroxisomal proliferator-activated receptors (PPAR) are a FA-response system involved in diverse cellular responses. FA regulate PPAR activity and modulate PPAR mRNA abundance. Increasing evidence indicates that PUFA are required for optimal neuronal development and function. To gain insight into the mechanism for nutrition-induced impairment of neuronal development and function we investigated the effect of chronic n-3 FA deficiency on PPAR mRNA levels in rat brain and ocular tissues. Rats were fed for three generations a diet designed to reduce DHA levels in tissues, and the abundance of PPARalpha and PPARbeta transcripts was measured by hybridization with specific probes. Chronic consumption of the a-linolenic acid (LNA)-insufficient diet caused a remarkable modification in DHA content in membrane phospholipids. The results reported here indicate that PPARa mRNA levels did not exhibit significant variation in ocular, hepatic, or nervous tissues from rats fed the experimental diet. In contrast, PPARalpha mRNA normalized to beta-actin mRNA was 21% higher in ocular tissue from F3 generation rats consuming the LNA-deficient diet but was independent of diet in hepatic and nervous tissues. The absolute abundance of PPARbeta transcripts showed a 17% increase in ocular tissue from rats consuming the LNA-deficient diet (F3 generation). The biological significance of the reported changes in PPARbeta mRNA in ocular tissue remains to be determined.


Asunto(s)
Ojo/metabolismo , Ácidos Grasos Omega-3/administración & dosificación , ARN Mensajero/genética , Receptores Citoplasmáticos y Nucleares/genética , Factores de Transcripción/genética , Actinas/genética , Animales , Femenino , Gliceraldehído-3-Fosfato Deshidrogenasas/genética , ARN Mensajero/metabolismo , Ratas , Ratas Long-Evans
7.
J Lipid Res ; 43(4): 611-7, 2002 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-11907144

RESUMEN

In this study, we have examined the effects of n-3 fatty acid deficient diets on the phospholipids (PL) molecular species composition in the hippocampus. Female rats were raised for two generations on diets containing linoleic acid (18:2n-6), with or without supplementation of alpha-linolenic acid (18:3n-3) or 18:3n-3 plus docosahexaenoic acid (22:6n-3). At 84 days of age, the hippocampal phospholipids were analyzed by reversed phase HPLC-electrospray ionization mass spectrometry. Depleting n-3 fatty acids from the diet led to a reduction of 22:6n-3 molecular species in phosphatidylcholine (PC), phosphatidylethanolamine (PE), PE-plasmalogens (PLE), and phosphatidylserine (PS) by 70-80%. In general, 22:6n-3 was replaced with 22:5n-6 but the replacement at the molecular species level did not always occur in a reciprocal manner, especially in PC and PLE. In PC, the 16:0,22:6n-3 species was replaced by 16:0,22:5n-6 and 18:0,22:5n-6. In PLE, substantial increases of both 22:5n-6 and 22:4n-6 species compensated for the decreases in 22:6n-3 species in n-3 fatty acid deficient groups. While the total PL content was not affected by n-3 deficiency, the relative distribution of PS decreased by 28% with a concomitant increase in PC. The observed decrease of 22:6n-3 species along with PS reduction may represent key biochemical changes underlying losses in brain-hippocampal function associated with n-3 deficiency.


Asunto(s)
Ácidos Grasos Omega-3/metabolismo , Hipocampo/química , Fosfatidilcolinas/química , Fosfatidiletanolaminas/química , Fosfatidilserinas/química , Plasmalógenos/química , Análisis de Varianza , Animales , Grasas Insaturadas en la Dieta/metabolismo , Femenino , Hipocampo/metabolismo , Fosfatidilcolinas/metabolismo , Fosfatidiletanolaminas/metabolismo , Fosfatidilserinas/metabolismo , Fosfolípidos/química , Fosfolípidos/metabolismo , Plasmalógenos/metabolismo , Ratas , Ratas Long-Evans
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