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1.
Int J Immunopathol Pharmacol ; 24(3): 673-81, 2011.
Article in English | MEDLINE | ID: mdl-21978699

ABSTRACT

Severe fatigue and a significantly reduced health-related quality of life (HRQoL) have been described in patients with chronic fatigue syndrome (CFS) in comparison with patients affected by chronic hepatitis C (CHC) and other chronic medical conditions. We examined 39 CFS and 49 CHC patients to explore whether fatigue and a poor HRQoL represent a greater medical and social problem in CFS than in CHC. The severity of fatigue and the HRQoL were assessed using the Fatigue Impact Scale (FIS) and the Health Status Questionnaire Short Form-36 (SF-36), respectively. The statistical analysis showed both a higher score of fatigue and a lower HRQoL in CFS than in CHC patients. Furthermore, in CHC patients the FIS evaluation showed a significantly reduced score of the psychosocial domain in comparison with the other domains. Multivariate linear regression analysis revealed female gender as the most important positive variable in chronic hepatitis C patients for total score of FIS. In conclusion, CFS was associated with a severe and disabling fatigue and an impaired HRQOL. In particular, both fatigue and all aspects of HRQOL perceived by CFS patients were significantly impaired compared to CHC patients. Consequently, management of fatigue should be considered a priority in order to improve HRQOL in CFS patients. In CHC patients the impact of fatigue on HRQoL was less significant than in CFS patients, even though the FIS evaluation showed a significant impairment of the psychosocial domain.


Subject(s)
Fatigue Syndrome, Chronic/physiopathology , Fatigue Syndrome, Chronic/psychology , Hepatitis C, Chronic/physiopathology , Hepatitis C, Chronic/psychology , Muscle Fatigue/physiology , Quality of Life/psychology , Adult , Aged , Fatigue Syndrome, Chronic/epidemiology , Female , Health Status , Hepatitis C, Chronic/epidemiology , Humans , Linear Models , Male , Middle Aged , Sex Factors , Socioeconomic Factors , Surveys and Questionnaires , Young Adult
2.
Virol J ; 7: 311, 2010 Nov 12.
Article in English | MEDLINE | ID: mdl-21070682

ABSTRACT

There have been reports of in-vitro interferon (IFN)-mediated antiviral activity against the hepatitis C virus (HCV) through microRNAs (miRNAs). The main aim of this study was to evaluate the expression of several miRNAs (miR-1, miR-30, miR-128, miR-196, miR-296) in peripheral blood mononuclear cells (PBMCs) from healthy individuals after in vitro IFN-treatment and in PBMCs from patients with chronic hepatitis C (CHC) before and 12 hours after the first injection of pegylated IFN alpha. We demonstrated that expression of these miRNAs could be recorded in PBMCs collected from healthy individuals before and after in-vitro IFN alpha treatment. Our analysis revealed that the levels of expression of all miRNAs investigated in patients with CHC were different to those in healthy individuals. When levels of the miRNAs were measured 12 hours after the first IFN injection, increases in expression levels of IFN-induced miRNAs were observed in 25-50% of patients, depending on the type of miRNA examined. No correlations were observed between HCV viral load, alanine aminotransferase status and expression of miRNA. Together these findings suggest that: (i) IFN alpha in-vitro treatment of PBMCs leads to a transcriptional induction of all miRNAs investigated; (ii) miRNAs can be induced differentially by IFN treatment in patients with HCV. Given the importance of miRNAs in defending the host against virus infections, it is possible that IFN-induced miRNAs may represent an important determinant of the clinical outcome of IFN therapy in HCV infection.


Subject(s)
Gene Expression , Hepatitis C, Chronic/immunology , Interferon-alpha/immunology , Interferon-alpha/therapeutic use , MicroRNAs/biosynthesis , Polyethylene Glycols/therapeutic use , Adult , Aged , Alanine Transaminase/blood , Female , Gene Expression Profiling , Humans , Interferon alpha-2 , Interferon-alpha/pharmacology , Leukocytes, Mononuclear/immunology , Male , Middle Aged , Polyethylene Glycols/pharmacology , Recombinant Proteins , Viral Load
3.
Infez Med ; 16(2): 91-3, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18622149

ABSTRACT

The bacterium Bartonella henselae causes cat scratch disease, a self-limited zoonotic disease which is common among children and adolescents. The most typical clinical presentation is a regional lymphadenopathy that commonly involves only a single node of cervical and axillary lymph nodes. Inguinal localization is rarely described. We report a case of a 35-year-old Caucasian male complaining of a painless right inguinal mass and slight fever. A diagnosis of Bartonella henselae infection was made according to the histopathological exam of the excised mass, that showed an inflammatory state likely due to Bartonella, and to the titre of antibodies for this agent. Cat scratch disease can occur at any age and may also involve inguinal lymph nodes. Therefore it should always be included in the differential diagnosis of lymphadenopathy for adults. It is important that a meticulous personal history is obtained and that a specific serological test and pathological examination of the lesions are carried out. Often antibiotic treatment is not required because it is a benign disease and often resolves spontaneously.


Subject(s)
Bartonella henselae , Cat-Scratch Disease , Lymphatic Diseases , Adult , Cat-Scratch Disease/diagnosis , Diagnosis, Differential , Groin , Humans , Lymph Nodes/pathology , Lymphatic Diseases/diagnosis , Lymphatic Diseases/pathology , Lymphatic Diseases/surgery , Male
4.
Ann Clin Lab Sci ; 36(1): 59-66, 2006.
Article in English | MEDLINE | ID: mdl-16501238

ABSTRACT

HIV-related metabolic abnormalities include hypertriglyceridemia, hypercholesterolemia, insulin resistance, and diabetes mellitus. Recent studies suggest a role of ghrelin in promoting the deposition of triglycerides (TG) in the liver and regulating the metabolic action of adiponectin. Visceral fat is a key regulator of inflammation and it secretes proinflammatory cytokines (eg, interleukin-18, IL-18), with potential atherogenic activity. The aim of this study was to assay serum concentrations of ghrelin, adiponectin, and IL-18 in HIV+ patients, with and without hypertriglyceridemia, who were receiving highly active antiretroviral therapy (HAART). The 49 HIV+ patients were divided in 2 groups: 17 patients with serum TG concentration >200 mg/dl (group A) and 32 patients with normal serum TG concentration (group B). All subjects underwent viral and immunological evaluations and determinations of serum cholesterol, glucose, ghrelin, adiponectin, and IL-18. No differences of viral and immunological parameters were observed between the 2 groups. Serum levels of ghrelin were 768 +/- 596 pg/dl in group A and 470 +/- 248 pg/dl in group B (p = 0.01). Group A had lower serum adiponectin levels (8.4 +/- 3.6 microg/dl) than group B (18.2 +/- 10.1 microg/dl; p = 0.0001). Serum IL-18 levels were 455 +/- 199 pg/ml in group A and 258 +/- 233 pg/ml in group B (p = 0.005). The patients with hypertriglyceridemia showed a positive correlation between serum triglyceride and ghrelin levels (r = 0.51, p = 0.03). These findings suggest potential roles of ghrelin, adiponectin, and IL-18 in the pathogenesis of metabolic disorders in HIV-infected patients.


Subject(s)
Adiponectin/blood , HIV Infections/blood , Hypertriglyceridemia/blood , Interleukin-18/blood , Peptide Hormones/blood , Adult , Antiretroviral Therapy, Highly Active , Female , Ghrelin , HIV Infections/complications , HIV Infections/drug therapy , Humans , Hypertriglyceridemia/etiology , Male
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