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2.
J Endocrinol Invest ; 46(2): 261-269, 2023 Feb.
Article de Anglais | MEDLINE | ID: mdl-36064879

RÉSUMÉ

PURPOSE: To retrospectively describe the association between thyroid hormones (TH) and platelet activation, as represented by mean platelet volume (MPV), in a cohort of patients hospitalized for COVID-19 with no known thyroid disease, and to correlate these data with the severity of COVID-19 and the occurrence of death/ARDS (Acute Respiratory Distress Syndrome). METHODS: 103 patients with real-time polymerase chain reaction (RT-PCR) testing-confirmed COVID-19 and hospitalized were enrolled. Serum samples were collected from patients upon admission before starting any treatment. Chi-squared test was used to determine the association between euthyroid sick syndrome (ESS) and COVID-19 severity. Multivariate logistic regression was performed to evaluate the best independent predictors of COVID-19 deaths/ARDS. RESULTS: 39/103 (37.9%) of patients were found to have ESS, and this condition was an independent predictor for the severity of COVID-19 (p = 0.003). Lower TSH and lower FT3/FT4 ratio correlated with higher MPV (p = 0,001 and p = 0.010), with an opposite trend with respect to what has been documented in non-COVID patients. Increasing MPV and lower FT3 significantly increased the risk, in COVID-19 patients, of an adverse outcome of death/ARDS. CONCLUSION: Increased platelet activation, as represented by increased MPV, has already been reported to correlate with COVID-19 severity, possibly as a consequence of cytokine release. We demonstrated, in a cohort of 103 patients with COVID-19, that MPV is inversely correlated to TH levels, in particular in the case of ESS, where downregulation of TH axis may occur in case of systemic cytokine inflammation and more severe outcomes (death/ARDS). That ESS itself may directly cause platelet activation, as demonstrated by higher MPV in these patients, is an interesting hypothesis which deserves further investigation.


Sujet(s)
COVID-19 , Humains , Études rétrospectives , Hormones thyroïdiennes , Hospitalisation , Activation plaquettaire
3.
Microbes Infect ; 23(4-5): 104808, 2021.
Article de Anglais | MEDLINE | ID: mdl-33753206

RÉSUMÉ

An unusual clonal gammopathy was reported in COVID-19 patient but whether this anomaly is related or not to the disease has not yet been clarified. To this aim, we selected a cohort of 35 COVID-19 patients swab positive and investigated serological levels of IL-6, immune response to major viral antigens and electrophoretic profile. Elevated levels of IL-6 were accompanied by a significative humoral response to viral Spike protein, revealing an altered electrophoretic profile in the gamma region. We can conclude that elevated levels of IL-6 triggers humoral response inducing a transient plasma cell dyscrasia in severe COVID-19 patients.


Sujet(s)
COVID-19/complications , Interleukine-6/immunologie , Paraprotéinémies/virologie , Sujet âgé , Anticorps antiviraux/sang , COVID-19/immunologie , Protéines de la nucléocapside des coronavirus/immunologie , Femelle , Humains , Italie , Mâle , Paraprotéinémies/immunologie , Phosphoprotéines/immunologie , Glycoprotéine de spicule des coronavirus/immunologie
8.
Parkinsonism Relat Disord ; 64: 342-345, 2019 07.
Article de Anglais | MEDLINE | ID: mdl-30956058

RÉSUMÉ

PNKP gene encodes for a kinase/phosphatase involved in DNA damage response, controlled and stabilized by ATM phosphorylation. PNKP deficiency, thus far described in 40 subjects, has been associated with a complex neurological phenotype encompassing microcephaly, seizures, developmental delay, ataxia, oculomotor apraxia and polyneuropathy. We report a new case expanding the clinical phenotype of this rare disorder. This 25 years old girl presented with chorea at the age of 2 years and remained stable up to the adult age when the emergence of fatigability and asthenia of lower limbs prompted a new examination disclosing a sensory-motor axonal demyelinating neuropathy. Clinical exome sequencing revealed two previously described variants in PNKP gene. This case highlights the phenotypic variability of PNKP associated disorders, showing that an early onset apparently non progressive chorea can be the presenting symptoms of this rare condition.


Sujet(s)
Enzymes de réparation de l'ADN/déficit , Enzymes de réparation de l'ADN/génétique , Troubles de la motricité/diagnostic , Maladies neurodégénératives/diagnostic , Phosphotransferases (Alcohol Group Acceptor)/déficit , Phosphotransferases (Alcohol Group Acceptor)/génétique , Polyneuropathies/diagnostic , Adulte , Chorée/diagnostic , Chorée/génétique , Femelle , Humains , Troubles de la motricité/génétique , Phénotype , Polyneuropathies/génétique
9.
Transplant Proc ; 51(1): 157-159, 2019.
Article de Anglais | MEDLINE | ID: mdl-30661898

RÉSUMÉ

BACKGROUND: BK virus (BKV)-associated nephropathy is definitely involved in allograft failure after kidney transplant. Thus, the need for an early control of viral reactivation in immunocompromised patients is well established. Determination of urinary release of decoy cells (DC) and BK viral load in plasma and urine by polymerase chain reaction (PCR) usually precedes renal biopsy. The aim of the study is to assess viral reactivation by BKV-DNA PCR and DC detection in urinary sediment using automated intelligent microscopy. METHODS: Seventy-eight kidney transplant patients were analyzed for the presence of plasma BKV-DNA by quantitative TaqMan real-time PCR. Additionally, automated intelligent microscopy was used for urine sediment analysis, allowing to count cells with decoy feature, confirmed by phase contrast microscopic review. RESULTS: Plasma BKV-DNA PCR was detected in 14 (17.9%) patients. DC were identified in 19 (24.3%) urine sediments by automated analyzers and confirmed by microscopic observation. Two patients were BKV-DNA-positive/DC-negative; conversely, 7 subjects were DC-positive/BKV-DNA-negative. CONCLUSIONS: Plasma quantification of BK viral load is currently the best noninvasive method for the detection of viral reactivation. Nevertheless, automated methods to screen for the presence of DC in urine could facilitate early BK virus replication diagnosis and patient follow-up by quantitative and visual results.


Sujet(s)
Maladies du rein/urine , Transplantation rénale , Microscopie/méthodes , Infections à polyomavirus/urine , Infections à virus oncogènes/urine , Adulte , Virus BK , ADN viral/sang , Femelle , Humains , Interprétation d'images assistée par ordinateur/instrumentation , Interprétation d'images assistée par ordinateur/méthodes , Sujet immunodéprimé , Maladies du rein/diagnostic , Maladies du rein/virologie , Mâle , Microscopie/instrumentation , Adulte d'âge moyen , Infections à polyomavirus/diagnostic , Infections à polyomavirus/immunologie , Réaction de polymérisation en chaine en temps réel , Transplantation homologue , Infections à virus oncogènes/diagnostic , Infections à virus oncogènes/immunologie , Examen des urines/instrumentation , Examen des urines/méthodes
10.
J Biol Regul Homeost Agents ; 32(6): 1599-1604, 2018.
Article de Anglais | MEDLINE | ID: mdl-30574772

RÉSUMÉ

Vitamin D may have prognostic value in hypertension patients and, in addition to conventional biomarkers, could be a valuable tool for disease management. The aim of this study was to assess the association of vitamin D status in patients with essential hypertension and to evaluate its prognostic utility. Forty-eight consecutive patients (40 Caucasian and 8 Asian) aged between 30 and 80 years (mean 61.5, range 34-84 years), were enrolled in the study. The main exclusion criteria were age less than 18 years, kidney failure, onco-hematologic disease, hypo-hyperparathyroidism, osteoporosis, treatment with bisphosphonate or 25(OH) vitamin D supplementation. Of the 48 patients included in the study, hyperlipidemia was described in 28, diabetes type 2 in 8, and ischemic heart disease in 14. Serum electrolytes, calcium, sodium, and potassium concentrations were within normal range. Low 25(OH) vitamin D levels inversely correlated with essential hypertension values (p less than 0.001) were considered extremely significant. The determination of 25(OH) vitamin D levels in patients with essential hypertension could improve the research for possible underlying conditions, which should be managed meticulously according to current guidelines.


Sujet(s)
Hypertension essentielle/sang , Vitamine D/sang , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Marqueurs biologiques/sang , Calcium/sang , Humains , Adulte d'âge moyen , Potassium/sang , Sodium/sang
11.
J Biol Regul Homeost Agents ; 32(4): 1039-1043, 2018.
Article de Anglais | MEDLINE | ID: mdl-30043591

RÉSUMÉ

The altered expression levels of S100 proteins can lead to four different categories of diseases: diseases of the heart and of the central nervous system, inflammatory disorders and cancer. Various studies have shown the lack of harmonization of the results obtained with different methods, mainly due to different performances and measurements of S100B. The purpose of this work was to compare quantitatively the fully automated Elecsys® immunoassay with the reference immunoenzimatic method CanAg® EIA for serum S100B protein. In the study serum samples were analyzed of 161 patients: 85 females (aged 22-83 years) and 76 males (aged 16-90 years), affected by oncological and non-oncological pathologies. Passing–Bablok regression was used to analyze the comparison between the assays; it showed a strong interassay correlation: r = 0.9350 (95% CI =0.9122 – 0.9520), with an intercept of 0.02063 (95% CI=-0.02850 – 0.01400) and a slope of 1.1125 (95% CI=1.0200 – 1.2417). Elecsys® S100 assay should be preferred to CanAg® S100 for better standardization, good reliability and precision but also with the aim to reduce costs and obtain results in a shorter time.


Sujet(s)
Marqueurs biologiques/sang , Test ELISA/méthodes , Mesures de luminescence/méthodes , Sous-unité bêta de la protéine liant le calcium S100/sang , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Techniques électrochimiques/méthodes , Femelle , Humains , Mâle , Adulte d'âge moyen , Jeune adulte
12.
J Biol Regul Homeost Agents ; 31(4): 1147-1154, 2017.
Article de Anglais | MEDLINE | ID: mdl-29254328

RÉSUMÉ

This study measured Procalcitonin (PCT), Presepsin (PRE-S) and pro-Adrenomedullin (pro-ADM) in intensive care unit (ICU) patient’s blood to assess their contribution to accurate diagnosis of sepsis and potential predictive impact on prognosis. The final aim was to improve the use of infection biomarkers for optimizing the impact of laboratory medicine on clinical outcomes, focusing on the good management of resources designed to produce maximum effectiveness and efficiency. Sixty-four adult patients were studied during their hospitalization in ICU; blood samples were collected and categorized according to their clinical diagnosis and illness severity, and sepsis marker levels were measured on automated immunoassay platforms. PCT, PRE-S and pro-ADM infection markers were significantly lower in controls than in sepsis or septic shock groups. The area under the curve, by ROC curve analysis, was 0.945 for PCT, 0.756 for PRE-S and 0.741 for pro-ADM. Sepsis diagnostic accuracy was not improved by combining PCT, PRE-S and pro-ADM measures. Preliminary data demonstrated that, despite PRE-S and pro-ADM being able to differentiate between septic and non-septic patients with accuracy, PCT remains the most reliable marker available. The results obtained still do not allow us to consider a combination of markers, because it would merely increase laboratory costs without improving diagnostic performance. Furthermore, the results confirm a possible prognostic role of pro-ADM in septic states, but no correlation between biomarker levels and survival at 48 h was detected. Hence PCT, PRE-S, nor pro-ADM can be used to predict short-term prognosis.


Sujet(s)
Adrénomédulline/sang , Calcitonine/sang , Antigènes CD14/sang , Fragments peptidiques/sang , Sepsie/sang , Sepsie/diagnostic , Adulte , Sujet âgé , Aire sous la courbe , Marqueurs biologiques/sang , Études cas-témoins , Femelle , Hospitalisation , Humains , Unités de soins intensifs , Mâle , Adulte d'âge moyen , Projets pilotes , Pronostic , Courbe ROC , Sepsie/mortalité , Sepsie/anatomopathologie , Indice de gravité de la maladie , Analyse de survie
13.
J Biol Regul Homeost Agents ; 31(3): 823-827, 2017.
Article de Anglais | MEDLINE | ID: mdl-28958142

RÉSUMÉ

Vitamin D may have prognostic value in cardiovascular disease (CVD) patients and, in addition to conventional biomarkers, could be a valuable tool for disease management. The aim of this study was to assess the association of vitamin D status in patients with acute coronary syndrome (ACS) and to evaluate its prognostic utility. The levels of 25(OH) vitamin D were correlated with troponin T hs. Forty-eight consecutive outpatients (40 Caucasian and 8 Asian) aged between 40 and 70 years (mean 61.5, range 43-77 years) were enrolled in the study. All patients were admitted to the Emergency Department with chest pain and suspected ACS. The main exclusion criteria were age <18 years, kidney failure, onco-haematological disease, hypo-hyperparathyroidism, hypo/hyperthyroidism, osteoporosis, treatment with bisphosphonate or 25(OH) vitamin D supplementation. Of the 48 subjects included in the study, thoracic pain symptoms were described in 12 patients with unstable angina (UA) and in 6 patients with ST elevation myocardial infarction (STEMI) and in 30 patients with non-ST-elevation myocardial infarction (NSTEMI). Low 25(OH) vitamin D levels correlated with the presence of ACS (p< 0.02) and inversely correlated with Troponin T hs (TnT hs) levels (p< 0.03). The determination of 25(OH) vitamin D levels in combination with TnT hs could improve the research for possible underlying conditions, and these should be managed meticulously according to current guidelines.


Sujet(s)
Syndrome coronarien aigu/sang , Infarctus du myocarde/sang , Vitamine D/analogues et dérivés , Adulte , Sujet âgé , Femelle , Humains , Mâle , Adulte d'âge moyen , Troponine T/sang , Vitamine D/sang
14.
J Biol Regul Homeost Agents ; 30(4): 1165-1171, 2016.
Article de Anglais | MEDLINE | ID: mdl-28078870

RÉSUMÉ

The “Risk of Malignancy Algorithm” (ROMA) combines the diagnostic power of the CA125 and HE4 markers with menopausal status to predict the risk for developing epithelial ovarian cancer (EOC). The aim of this study was to evaluate the association between 25-OH vitamin D levels and ROMA score in obese women. One hundred and eighteen patients with a Body Mass Index (BMI) > 30 kg/m2 (Group 1) and 80 women with a BMI less than 25 kg / m² (Group 2) were studied. The 25-OH vitamin D was quantified with LUMIPULSE® G 1200. As a threshold value, identified by ROC curve analysis, 20.2 ng/ mL (sensitivity 73.3%, specificity 84%) was chosen corresponding to the limit between sufficient and insufficient 25-OH vitamin D according to the World Health Organization (WHO). Low 25-OH vitamin D levels were observed in 64% of obese women and in 11% of normal-weight women (p less than 0.001). ROMA score above 13% was detected only in obese women (19%). An association between low levels of 25-OH vitamin D and ROMA score was observed. Indeed, 64% of obese women with ROMA score >13% had concomitant insufficient levels of 25-OH vitamin D, while only 36% of obese women with ROMA score >13% had sufficient 25-OH vitamin D levels (p less than 0.0001). This study suggests that the deficiency of 25- OH vitamin D in obese women has a possible correlation with high ROMA score.


Sujet(s)
Marqueurs biologiques tumoraux/sang , Obésité/sang , Vitamine D/analogues et dérivés , Adulte , Algorithmes , Densité osseuse , Carcinome épithélial de l'ovaire , Test ELISA , Femelle , Humains , Adulte d'âge moyen , Tumeurs épithéliales épidermoïdes et glandulaires/sang , Tumeurs épithéliales épidermoïdes et glandulaires/complications , Obésité/complications , Tumeurs de l'ovaire/sang , Tumeurs de l'ovaire/complications , Courbe ROC , Facteurs de risque , Sensibilité et spécificité , Vitamine D/sang , Jeune adulte
15.
Article de Anglais | MEDLINE | ID: mdl-24110209

RÉSUMÉ

The time-varying gradient fields generated during Magnetic Resonance Imaging (MRI) procedures have the potential to induce electrical current on implanted endocardial leads. Whether this current can result in undesired cardiac stimulation is unknown. This paper presents an optically coupled system with the potential to quantitatively measure the currents induced by the gradient fields into endocardial leads during MRI procedures. Our system is based on a microcontroller that works as analog-to-digital (A/D) converter and sends the current signal acquired from the lead to an optical high-speed light-emitting-diode transmitter. Plastic fiber guides the light outside the MRI chamber, to a photodiode receiver and then to an acquisition board connected to a PC. The preliminary characterization of the performances of the system is also presented.


Sujet(s)
Défibrillateurs implantables , Pacemaker , Artéfacts , Humains , Champs magnétiques , Imagerie par résonance magnétique , Dispositifs optiques
17.
Med Biol Eng Comput ; 41(5): 550-5, 2003 Sep.
Article de Anglais | MEDLINE | ID: mdl-14572005

RÉSUMÉ

This paper describes a portable heart simulator for the study of electromagnetic interference with active implantable devices. The simulator consists of plexiglas box divided into three chambers simulating the left atrium and the ventricles, plus a lateral compartment for the implantable device. The box is linked to a laptop computer by an analogue-to-digital convertor board, and the three chambers are monitored and driven by dedicated hardware and software interfaces. Synthetic endocardial atrial and ventricle signals for 13 cardiac rhythms are stored in the computer. They are applied to the cardiac chambers by AgCl plates. Sensing electrodes are in the form of AgCl needles inserted in saline. The simulator was able to demonstrate the behaviour of three pacemakers tested in the absence and presence of electromagnetic interference, generated by mobile phones (European GSM 900 and 1800 MHz) that emitted up to 2W (1 W at 1800 MHz). Pacemakers can be programmed with sensitivity from 0.1 mV to 5 mV, pulse width from 0.1 ms to 1.5 ms and pulse amplitude from 0.5 V to 5 V. The structural separation in three cardiac chambers (plus the one for the device) allowed a fast analysis procedure for dual- and tri-chamber implantable devices.


Sujet(s)
Champs électromagnétiques , Modèles cardiovasculaires , Pacemaker , Téléphones portables , Conception d'appareillage , Humains
18.
J Med Virol ; 65(2): 368-72, 2001 Oct.
Article de Anglais | MEDLINE | ID: mdl-11536246

RÉSUMÉ

The human herpesvirus-8 (HHV-8) has been associated with the development of Kaposi's sarcoma. A high incidence of classic Kaposi's sarcoma has been described in Sardinia, an island West of Italy's mainland. Different seroepidemiological analyses have reported that prevalence of HHV-8 infection varies worldwide: a high HHV-8 seroprevalence has been shown in Italy. The present survey was carried out to evaluate the correlation between HHV-8 infection and classic Kaposi's sarcoma incidence in northern Sardinia. Blood samples were collected from 226 healthy donors born and resident in five different areas of North Sardinia. Seroprevalence to HHV-8 was determined searching antibodies to viral lytic proteins by immunofluorescence in sera diluted at 1:10. Classic Kaposi's sarcoma incidence data spanning a period of 23 years were examined in the areas studied. The present screening revealed that seroprevalence was 35%, within a range of 15.3-46.3% in the five areas, although it should be considered that the seroprevalence to HHV-8 can be established more accurately by the combined use of different assays. Age emerged as an important risk factor. Indeed, subjects aged > 50 years showed a higher seroprevalence to HHV-8 as compared with younger individuals. A strong direct correlation between HHV-8 prevalence and classic Kaposi's sarcoma incidence has been also observed. The wide diffusion of HHV-8 in Sardinia appears to represent an important factor in the high incidence of classic Kaposi's sarcoma reported in the island. However, additional co-factors, such as age, sex, genetic traits, or viral strain pathogenicity, are likely to play a role in the development of the disease.


Sujet(s)
Anticorps antiviraux/sang , Herpèsvirus humain de type 8/immunologie , Sarcome de Kaposi/épidémiologie , Adulte , Femelle , Humains , Italie/épidémiologie , Mâle , Adulte d'âge moyen , Facteurs de risque , Sarcome de Kaposi/sang , Études séroépidémiologiques
20.
J Virol ; 74(7): 3235-44, 2000 Apr.
Article de Anglais | MEDLINE | ID: mdl-10708440

RÉSUMÉ

Computer analysis of the Epstein-Barr virus (EBV) genome indicates there are approximately 100 open reading frames (ORFs). Thus far about 30 EBV genes divided into the categories latent and lytic have been identified. The BamHI F region of EBV is abundantly transcribed during lytic replication. This region is highly conserved among herpesviruses, thus suggesting that some common function could be retained in the ORFs encompassed within this viral fragment. To identify putative novel proteins and possible new markers for viral replication, we focused our attention on the first rightward ORF in the BamHI F region (BFRF1). Histidine and glutathione S-transferase-tagged BFRF1 fusion proteins were synthesized to produce a mouse monoclonal antibody (MAb). Analysis of human sera revealed a high seroprevalence of antibodies to BFRF1 in patients affected by nasopharyngeal carcinoma or Burkitt's lymphoma, whereas no humoral response to BFRF1 could be detected among healthy donors. An anti-BFRF1 MAb recognizes a doublet migrating at 37 to 38 kDa in cells extracts from EBV-infected cell lines following lytic cycle activation and in an EBV-negative cell line (DG75) transfected with a plasmid expressing the BFRF1 gene. Northern blot analysis allowed the detection of a major transcript of 3.7 kb highly expressed in EBV-positive lytic cycle-induced cell lines. Treatment with inhibitors of viral DNA polymerase, such as phosphonoacetic acid and acyclovir, reduced but did not abolish the transcription of BFRF1, thus indicating that BFRF1 can be classified as an early gene. Cell fractionation experiments, as well as immunolocalization by immunofluorescence microscopy, immunohistochemistry, and immunoelectron microscopy, showed that BFRF1 is localized on the plasma membrane and nuclear compartments of the cells and is a structural component of the viral particle. Identification of BFRF1 provides a new marker with which to monitor EBV infection and might help us better understand the biology of the virus.


Sujet(s)
Herpèsvirus humain de type 4/génétique , Protéines membranaires/génétique , Protéines virales/génétique , Séquence d'acides aminés , Animaux , Anticorps monoclonaux/génétique , Anticorps monoclonaux/immunologie , Lignée cellulaire , Gènes viraux , Herpèsvirus humain de type 4/physiologie , Humains , Protéines membranaires/composition chimique , Protéines membranaires/immunologie , Souris , Données de séquences moléculaires , Cadres ouverts de lecture , ARN messager/génétique , Protéines recombinantes/génétique , Protéines virales/composition chimique , Protéines virales/immunologie , Réplication virale/génétique
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