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1.
Eur J Neurol ; 21(2): 267-72, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24238370

ABSTRACT

BACKGROUND AND PURPOSE: Migraine is a common neurological disorder. It can be divided into episodic migraine (EM) and chronic migraine (CM), based on headache frequency. Some studies have shown that insulin sensitivity is impaired in migraine; moreover, hypertension, diabetes and obesity are common in patients with CM. The aim of this study was to assess serum glucose, insulin levels and insulin resistance (IR) in a sample of episodic migraineurs, chronic migraineurs and non-pain healthy controls. METHODS: Eighty-three women with EM, 83 with CM and 83 healthy controls were recruited. Headache was diagnosed according to the latest International Classification of Headache Disorders 2 criteria. Waist circumference, body mass index (BMI) and blood pressure were measured. Checked metabolic parameters included fasting glucose, the 2 h 75 g oral glucose tolerance test (2 h OGTT), serum HbA1c, blood lipid profile, C-reactive protein and prolactin. The homeostasis model assessment formula was used to calculate IR. RESULTS: A significant prevalence of IR in CM was observed (P = 0.002). No significant associations were found with fasting glycaemia, the 2 h OGTT, HbA1c, blood lipid profile, C-reactive protein, prolactin and waist circumference. Obesity (BMI >30 kg/m(2)) was associated with an increased risk of CM [odds ratio (OR) 2.4]. When the outcome of interest was the association between IR and obesity, the OR was significantly increased compared with IR alone (OR = 13.2). CONCLUSION: This may suggest that CM is associated with IR status, particularly when it is in partnership with obesity.


Subject(s)
Blood Glucose/metabolism , Insulin Resistance/physiology , Migraine Disorders/physiopathology , Obesity/physiopathology , Adult , Body Mass Index , Cross-Sectional Studies , Female , Glucose Tolerance Test , Humans , Middle Aged , Migraine Disorders/complications , Obesity/complications , Waist Circumference
2.
Eur J Gynaecol Oncol ; 32(3): 303-6, 2011.
Article in English | MEDLINE | ID: mdl-21797122

ABSTRACT

Uterine cancer is today the upcoming neoplasia in gynaecological oncology. In Western countries endometrial cancer is mostly diagnosed after menopause and often becomes apparent with atypical uterine bleeding. Because of the great importance of such disease a series of accurate diagnostic analyses which require an adequate expenditure by hospital structures become necessary. Transvaginal sonography (TVS) remains the first choice to diagnose atypical bleeding because it is less invasive and highly bearable by the patients. TVS exam allows the selection of all patients who have an endometrial thickness more than 5 mm and/or with an inhomogeneous endometrial line thickness, who would then undergo further analyses. To achieve the diagnosis, office hysteroscopy carried out in an outpatient departments, is the most useful exam. Such exam allows a complete overview of the uterine cavity with possible detection of smaller lesions and a specific sampling of histological material. Hysteroscopy is today an indispensable aid in last resort diagnosis of endometrial cancer and is highly tolerated by patients.


Subject(s)
Carcinoma/diagnosis , Endometrial Neoplasms/diagnosis , Hysteroscopy/methods , Menopause , Uterus/pathology , Aged , Female , Humans , Middle Aged , Outpatients , Uterine Hemorrhage/diagnosis
3.
Acta Neurol (Napoli) ; 13(6): 534-8, 1991 Dec.
Article in English | MEDLINE | ID: mdl-1805554

ABSTRACT

We report the genealogical, clinical and molecular genetic findings of a new family with autosomal dominant early-onset Alzheimer's disease (FAD) discovered in Torino (Italy). Up to now, the pedigree comprises 1500 members, distributed in 8 generations. 22 patients affected with Alzheimer's disease have been identified. The clinical course of the disease was fairly uniform in all the patients. An high incidence of myoclonic jerks and epileptic seizures was found. Molecular genetic studies showed the presence of positive but nonsignificant lod scores between chromosome 21 anonymous DNA markers and the disease. The data obtained from the Torino family were computed together with those of additional 47 pedigrees, with both early-onset and late-onset Alzheimer's disease. A predisposing locus for the disease was found on the pericentromeric region of chromosome 21 only in early-onset FAD pedigrees.


Subject(s)
Alzheimer Disease/genetics , Phenotype , Adult , Alzheimer Disease/diagnosis , Chromosome Aberrations/genetics , Chromosome Disorders , Female , Genes, Dominant/genetics , Genetic Carrier Screening , Genetic Markers/genetics , Humans , Italy
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