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1.
J Gastroenterol Hepatol ; 24(7): 1163-8, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19682190

ABSTRACT

BACKGROUND AND AIM: Thyroid dysfunction is the most common endocrinopathy associated with hepatitis C and its interferon-based treatment. When undergoing treatment, interferon and ribavirin synergize to potently stimulate the immune system in order to eradicate the virus. One of the innocent bystanders in this accentuated response is the thyroid. The present study investigated whether thyroid dysfunction while undergoing combination treatment for hepatitis C is a favorable prognostic maker for a sustained virological response. METHODS: We carried out a prospective clinical audit in 201 patients treated with combination ribavirin and alpha-interferon and determined the prevalence of sustained virological response in patients in association with thyroid disease. A meta-analysis was also carried out pooling 741 patients from four previous studies on this topic. RESULTS: There was positive and significant association between thyroid disease and viral clearance. This was not supported by the meta-analysis, however, and some plausible explanations are proffered for this inconsistency. CONCLUSION: Despite lacking supportive evidence from the meta-analysis, it is important that this information is confirmed (or refuted) in future studies.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis C, Chronic/drug therapy , Interferon-alpha/therapeutic use , Ribavirin/therapeutic use , Thyroid Diseases/chemically induced , Adult , Antiviral Agents/adverse effects , Clinical Audit , Drug Therapy, Combination , Evidence-Based Medicine , Female , Hepacivirus/drug effects , Hepacivirus/genetics , Hepatitis C, Chronic/diagnosis , Humans , Interferon-alpha/adverse effects , Male , Middle Aged , Odds Ratio , Prospective Studies , RNA, Viral/blood , Ribavirin/adverse effects , Risk Assessment , Time Factors , Treatment Outcome , Viral Load
2.
Endocr J ; 52(1): 103-9, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15758565

ABSTRACT

Cushing's syndrome and its various aetiologies is a markedly difficult diagnosis to make given its subtle signs, sometime cyclical nature, and the lack of a single definitive diagnostic test. Although a great variety of diagnostic tests have been developed to assist in the diagnosis, even with the best clinical acumen, biochemistry and medical imaging the diagnosis can remain elusive. The long low and high dose oral dexamethasone suppression test is cumbersome, costly and often requiring an extended inpatient stay. The utility of the dexamethasone suppression test would be greatly enhanced if it could be performed as a short outpatient procedure. In this study we sought to confirm and refine the clinical utility of the high dose 4 mg intravenous dexamethasone suppression test as an alternative diagnostic test for Cushing's syndrome. There were a total of 31 subjects: 8 patients with proven pituitary Cushing's disease, 3 with primary adrenal tumors, 10 with pseudo-Cushing's syndrome and 10 healthy controls. All subjects with pseudo-Cushing's syndrome suppress serum cortisol at +5 and at +24 hours. In subjects with pituitary Cushing's disease, 7 out of 8 (88%) had serum cortisol suppressed at +5 hours but rebounded at +24 hours to at least 70% of the original serum level. Primary adrenal tumors showed a pattern of non-suppression throughout. The 4 mg intravenous dexamethasone suppression test is excellent in ruling out pseudo-Cushing's syndrome. This test is much simpler and more convenient than the oral dexamethasone suppression test in confirming clinical suspicion of pituitary Cushing's disease.


Subject(s)
Cushing Syndrome/blood , Cushing Syndrome/diagnosis , Dexamethasone , Glucocorticoids , Hydrocortisone/blood , Adrenal Gland Neoplasms/blood , Adrenal Gland Neoplasms/diagnosis , Adult , Aged , Dexamethasone/administration & dosage , Diagnosis, Differential , Dose-Response Relationship, Drug , Female , Glucocorticoids/administration & dosage , Humans , Injections, Intravenous , Male , Middle Aged , Time Factors
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