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1.
Am J Med Genet B Neuropsychiatr Genet ; 156B(6): 700-8, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21714072

RESUMEN

DNA methylation may mediate persistent changes in gene function following chronic stress. To examine this hypothesis, we evaluated African American subjects matched by age and sex, and stratified into four groups by post-traumatic stress disorder (PTSD) diagnosis and history of child abuse. Total Life Stress (TLS) was also assessed in all subjects. We evaluated DNA extracted from peripheral blood using the HumanMethylation27 BeadChip and analyzed both global and site-specific methylation. Methylation levels were examined for association with PTSD, child abuse history, and TLS using a linear mixed model adjusted for age, sex, and chip effects. Global methylation was increased in subjects with PTSD. CpG sites in five genes (TPR, CLEC9A, APC5, ANXA2, and TLR8) were differentially methylated in subjects with PTSD. Additionally, a CpG site in NPFFR2 was associated with TLS after adjustment for multiple testing. Notably, many of these genes have been previously associated with inflammation. Given these results and reports of immune dysregulation associated with trauma history, we compared plasma cytokine levels in these subjects and found IL4, IL2, and TNFα levels associated with PTSD, child abuse, and TLS. Together, these results suggest that psychosocial stress may alter global and gene-specific DNA methylation patterns potentially associated with peripheral immune dysregulation. Our results suggest the need for further research on the role of DNA methylation in stress-related illnesses.


Asunto(s)
Citocinas/inmunología , Metilación de ADN/genética , Trastornos por Estrés Postraumático/genética , Estrés Psicológico/genética , Adultos Sobrevivientes del Maltrato a los Niños , Negro o Afroamericano , Islas de CpG/genética , Citocinas/biosíntesis , Citocinas/sangre , ADN , Metilación de ADN/inmunología , Humanos , Trastornos por Estrés Postraumático/inmunología , Trastornos por Estrés Postraumático/metabolismo , Estrés Psicológico/inmunología
2.
Endocr Pract ; 10(4): 335-8, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15760777

RESUMEN

OBJECTIVE: To report an uncommon case of osteogenic sarcoma of the sella turcica after radiation treatment of a pituitary adenoma. METHODS: We present the clinical history, physical findings, laboratory data, imaging studies, and pathologic findings in a patient found to have osteogenic sarcoma of the sella after radiation therapy for a nonfunctioning pituitary adenoma. RESULTS: Six years after transsphenoidal resection and postoperative fractionated radiation therapy for a nonfunctioning pituitary adenoma that extended to the cavernous sinus, a 45-year-old man presented with a sinus infection, diplopia, and ophthalmoplegia of the right eye. A computed tomographic scan of the head showed a mass in the sella with involvement of the optic chiasm and right cavernous sinus. Transsphenoidal resection and debulking of the tumor revealed an osteogenic sarcoma. The patient was discharged from the hospital with residual diplopia and ophthalmoplegia. He was treated with levothyroxine, testosterone, and hydrocortisone. Six weeks later, the patient was readmitted after he was found unresponsive, and computed tomographic scans disclosed a massive cerebrovascular accident. He died a few days later. CONCLUSION: Osteogenic sarcoma is a rare, late complication of radiation treatment of pituitary adenoma. Although radiotherapy remains an effective adjunctive treatment in patients with pituitary adenomas, particularly those with residual or recurrent tumor, potential complications must be acknowledged.


Asunto(s)
Neoplasias Inducidas por Radiación/etiología , Osteosarcoma/etiología , Radioterapia/efectos adversos , Neoplasias Craneales/etiología , Adenoma/terapia , Resultado Fatal , Humanos , Masculino , Persona de Mediana Edad , Neoplasias Inducidas por Radiación/terapia , Procedimientos Neuroquirúrgicos/métodos , Osteosarcoma/terapia , Neoplasias Hipofisarias/terapia , Silla Turca , Neoplasias Craneales/terapia
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