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1.
Nutr Metab Cardiovasc Dis ; 25(12): 1104-10, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26615224

ABSTRACT

BACKGROUND AND AIMS: Increased carotid artery intima-media thickness (IMT) and the presence of plaques have been shown to be predictors of cardiovascular disease. The cardiovascular risk in patients with overt thyroid diseases is related to increased risk of atherosclerosis, but there has been no clear evidence about subclinical disorders. We have assessed whether subclinical thyroid dysfunction is associated with arterial thickening and plaque. METHODS AND RESULTS: The SardiNIA study is a population-based survey on the Italian island of Sardinia. We reviewed data from 5815 subjects (aged 14-102 years), none of whom had overt hyperthyroidism or hypothyroidism or was taking thyroid medication. Serum thyrotropin (TSH), free thyroxine, together with carotid ultrasound IMT and the presence of common carotid plaques were analysed in all subjects. Possible association of IMT and carotid plaques with thyroid parameters was evaluated by univariate and multivariate analyses. IMT was significantly associated with age, sex, smoking, low density lipoprotein cholesterol (LDL), high density lipoprotein cholesterol, pulse pressure (PP), history of arterial hypertension, diabetes, and previous cardiovascular events (p = 0.001 or lower, R(2) = 0.47). Carotid plaques were predicted by age, sex, LDL, PP, history of diabetes, previous cardiovascular events, and the use of statins (p = 0.029 or lower). Thyroid hormone was not predictive of carotid atherosclerosis when adjusted for confounders. CONCLUSION: Thyroid hormone is not associated with increased IMT or with the presence of carotid artery plaque. Our data do not support the idea that treating subclinical disorders might help to prevent arterial remodelling or carotid atherosclerosis.


Subject(s)
Cardiovascular Diseases/epidemiology , Carotid Artery Diseases/epidemiology , Carotid Intima-Media Thickness , Carotid Stenosis/epidemiology , Thyroid Diseases/epidemiology , Adult , Age Factors , Aged , Analysis of Variance , Cardiovascular Diseases/diagnosis , Carotid Artery Diseases/diagnostic imaging , Carotid Stenosis/diagnostic imaging , Comorbidity , Confidence Intervals , Cross-Sectional Studies , Female , Humans , Hyperthyroidism/diagnosis , Hyperthyroidism/epidemiology , Hypothyroidism/diagnosis , Hypothyroidism/epidemiology , Longitudinal Studies , Male , Middle Aged , Multivariate Analysis , Odds Ratio , Risk Assessment , Sensitivity and Specificity , Sex Factors , Thyroid Diseases/diagnosis , Thyroid Function Tests
2.
Nutr Metab Cardiovasc Dis ; 19(8): 532-41, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19321325

ABSTRACT

AIM: We investigated the gender-specific control of cardiovascular (CV) risk factors and subclinical vascular lesions in a founder population in Italy. METHODS AND RESULTS: 6148 subjects were enrolled (aged 14-102 years) from four towns. Hypertension (HT), diabetes mellitus (DM) and dyslipidemia (LIP) were defined in accordance with guidelines. A self-reported diagnosis defined awareness of these conditions, and the current use of specific medications as treatment. Prevalence was HT 29.2%, DM 4.8%, LIP 44.1% and was higher in men than in women. Disease prevalence increased with age for every CV risk factor. Men were less likely than women to take anti-HT drugs and to reach BP control (9.9% vs. 16%). Only 17.6% of HT > 65 years had a BP < or =140/90 mmHg, though 48.5% were treated. The use of statins was very low (<1/3 of eligible subjects > 65 years, those with the highest treatment rate). The ratio of control-to-treated HT was lower in subjects with, than in those without, thicker carotid arteries (31.5% vs. 38.8%, p < 0.05) or stiffer aortas (26.0% vs. 40.0%, p < 0.05) or carotid plaques (26.3% vs. 41.1%, p<0.05). CONCLUSION: A large number of subjects at high CV risk are not treated and the management of subclinical vascular lesions is far from optimal.


Subject(s)
Awareness , Cardiovascular Diseases/prevention & control , Diabetes Mellitus/drug therapy , Dyslipidemias/drug therapy , Health Knowledge, Attitudes, Practice , Hypertension/drug therapy , Metabolic Syndrome/drug therapy , Obesity/drug therapy , Adolescent , Adult , Age Factors , Aged , Aged, 80 and over , Antihypertensive Agents/therapeutic use , Atherosclerosis/complications , Atherosclerosis/drug therapy , Atherosclerosis/epidemiology , Cardiovascular Diseases/epidemiology , Cardiovascular Diseases/etiology , Diabetes Mellitus/epidemiology , Drug Utilization , Dyslipidemias/complications , Dyslipidemias/epidemiology , Female , Founder Effect , Guideline Adherence , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Hypertension/complications , Hypertension/epidemiology , Hypoglycemic Agents/therapeutic use , Italy/epidemiology , Male , Metabolic Syndrome/complications , Metabolic Syndrome/epidemiology , Middle Aged , Obesity/complications , Obesity/epidemiology , Practice Guidelines as Topic , Practice Patterns, Physicians' , Prevalence , Risk Assessment , Risk Factors , Sex Factors , Young Adult
3.
J Int Med Res ; 7(5): 351-3, 1979.
Article in English | MEDLINE | ID: mdl-499642

ABSTRACT

In thirty-two patients, divided into four groups: normal, G-6-PD deficient, beta-thalaxemic heterozygote and carriers of both anomalies, the variations in erythrocyte GSH were studied after incubation with APH and a non-steroidal anti-inflammatory drug: tolmetin sodium. The results obtained show a considerable fall in GSH after incubation with APH above all in the G-6-PD deficient patients and in the carriers of both anomalies. On the other hand, after incubation with the drug under examination there were no significant variations in the erythrocyte GSH.


Subject(s)
Erythrocytes/metabolism , Glucosephosphate Dehydrogenase Deficiency/blood , Glutathione/blood , Pyrroles/pharmacology , Tolmetin/pharmacology , Adult , Aged , Depression, Chemical , Erythrocytes/drug effects , Glucosephosphate Dehydrogenase Deficiency/complications , Humans , In Vitro Techniques , Male , Middle Aged , Thalassemia/blood , Thalassemia/complications
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