Trappolini M
Sapienza University of Rome
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Publication
Featured researches published by Trappolini M.
Annals of Medicine | 2010
Flavia Del Porto; Maria Proietta; Luigi Tritapepe; Fabio Miraldi; Angela Koverech; Patrizia Cardelli; Fabio Tabacco; Vincenzo De Santis; Andrea Vecchione; Anna Paola Mitterhofer; Italo Nofroni; Rachele Amodeo; Trappolini M; Giuseppe Aliberti
Abstract Objective. The aim of our study was to evaluate the lymphocyte subpopulations and the cytokines in the peripheral blood of patients with type-A Stanford acute aortic dissection (AAD group) and to determine whether inflammatory cells are present at the site of aortic dissection. Methods. Thirty-five consecutive patients with type-A Stanford dissection were evaluated for haemochrome and lymphocyte subpopulations (CD3+, CD4+, CD8+, CD19+, CD4+CD25+, CD16+CD56+, CD4+CD28−, CD8+CD28−) by flow cytometry. C-reactive protein (CRP), tumour necrosis factor (TNF)-α, interleukin (IL)-2, IL-4, IL-6, IL-8, IL-10, interferon-gamma (IFN-γ), and monocyte chemoattractant protein (MCP)-1 were measured by ELISA. In addition, immunohistochemical staining with cell type-specific antibodies was performed to study the inflammatory cells detected inside the aortic wall. Results. In the AAD group, a significant increase in natural killer (NK) (P = 0.032), B cells (P = 0.022), and CD8+CD28− (P = 0.045) subpopulations was observed, whereas there was a significant decrease in total T lymphocytes (P = 0.004) and T helper fractions (P = 0.005). Moreover, a significant increase in CRP (P < 0.0001), IL-6 (P < 0.0001), IL-8 (P < 0.0001), IL-10 (P < 0.0001), TNF-α (P < 0.0001), and MCP-1 (P < 0.001) was observed; macrophages represented the main population detected inside the media. Conclusions. Our results strongly support the hypothesis of a pivotal role of innate immunity in type-A Stanford AAD.
Best Practice & Research Clinical Endocrinology & Metabolism | 2010
Antonietta Colatrella; Valentina Loguercio; Luca Mattei; Trappolini M; Camilla Festa; Michela Stoppo; Angela Napoli
Hypertensive disorders in pregnancy can be chronic, pregestational or just diagnosed before the 20th week, or newly diagnosed in the second half of pregnancy. Any type of hypertension is more frequent in diabetic pregnancies with a different distribution among different types of diabetes. Most of the evidence is for pre-eclampsia associated with a marked increase in primary caesarean section, preterm birth and more need for neonatal intensive care. Different risk factors and pregnancy outcomes would support the hypothesis that pre-eclampsia and gestational hypertension might be largely separate entities, but this position is not unanimously accepted. Chronic hypertension increases with age and duration of diabetes, predicting increased rates of prematurity and neonatal morbidity, especially when associated with superimposed pre-eclampsia. Long-term consequences are observed in women whose pregnancy was complicated by hypertension such as chronic hypertension and cardiovascular diseases.
Lupus | 2011
F Del Porto; Maria Proietta; A. Koverech; Trappolini M; Giuseppe Aliberti
Hypercalcaemia is found in more than 90% of the cases of primitive hyperparathyroidism and malignancies. Rarely, D hypervitaminosis, sarcoidosis, other granulomatous diseases, some drugs, and endocrine diseases may be responsible. Nine patients with systemic lupus erythematosus (SLE) and hypercalcaemia, without evidence of primary hyperparathyroidism, have been previously described. Here we report the 10th patient with SLE and hypercalcaemia, along with a brief review of the literature.
Lupus | 2009
F Del Porto; Maria Proietta; A Stoppacciaro; Trappolini M; P Menè; Giuseppe Aliberti
Differential diagnosis in patients presenting with fever of unknown origin (FUO) is often difficult because infectious diseases, neoplasms, infective endocarditis or systemic autoimmune diseases may all be responsible for the condition. Furthermore, vasculitis may generate typical, atypical or limited syndromes depending on the extent of vascular involvement. Here, we report the case of a 73-year-old man with FUO and renal failure due to a rare variant of Wegener’s granulomatosis, limited to the kidneys.
Blood Coagulation & Fibrinolysis | 2010
Giuseppe Aliberti; Maria Proietta; Isabella Pulignano; Flavia Del Porto; Andrea Tammeo; Trappolini M
Minerva Cardioangiologica | 2006
Trappolini M; Scorza A; Chillotti Fm; Trappolini F; Danese A; De Vito F; Luberti E; Angrisani L; Braucci S
Clinica Terapeutica | 2008
Trappolini M; Scorzai A; Loguercio; Stoppo M; Sebastianelli A; Iannotta M; Del Porto F; Proietta M; Aliberti G
Recenti progressi in medicina | 2009
Trappolini M; Michela Stoppo; Marilla Meggiorini; Valentina Loguercio; Ombretta Fabiani; Marco Iannotta; Andrea Negro; Alisa Sebastianelli; Maria Proietta; Flavia Del Porto; Giuseppe Aliberti
Clinica Terapeutica | 2007
Braucci S; Trappolini F; Angrisani L; Luberti E; Clarice A; Proietta M; Pisani D; Trappolini M
Minerva Cardioangiologica | 2001
Matteoli S; Trappolini M; Chillotti Fm