Impact des mutations germinales du gène AIP sur les caractéristiques tumorales et la prise en charge médicale chez les patients acromégales jeunes : résultats d'une étude sur des populations appariées pour l'âge et le diamètre de la tumeurBeckers, Albert ; ; et alin Annales d'Endocrinologie - 28ème congrès de la société Française d'Endocrinologie (2011) Detailed reference viewed: 15 (0 ULg) Drospirenone and interference with renin-antiotensin systemVROONEN, Laurent ; Cavalier, Etienne ; et alin Annales d'Endocrinologie - 28ème congrès de la société Française d'Endocrinologie (2011) Detailed reference viewed: 37 (1 ULg) The Thyro-gastric syndrome : its prevalence, clinical, pathological and predictive factors in a prospective series of 360 patients with Hashimoto's Thyroiditis; VALDES SOCIN, Hernan Gonzalo ; LUTTERI, Laurence et alin Abstract book - 21st Meeting of the Belgian Endocrine Society (2011) Detailed reference viewed: 94 (4 ULg) Une nouvelle forme d'adénomes hypophysaires familiaux : les FIPA-Détection et prise en chargeBeckers, Albert ; PETROSSIANS, Patrick ; et alin Correspondances en MHDN (2011) Detailed reference viewed: 16 (5 ULg) Influence of drospirenone on renin-angiotensin-aldosterone system evaluationVROONEN, Laurent ; Cavalier, Etienne ; et alin Endocrine Abstracts - 13th European Congress of Endocrinology (2011) Detailed reference viewed: 22 (2 ULg) Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas - An International Collaborative StudyDaly, Adrian ; ; Petrossians, Patrick et alin Journal of Clinical Endocrinology and Metabolism (2010), 95(11), Context: AIP mutations (AIPmut) give rise to a pituitary adenoma predisposition that occurs in familial isolated pituitary adenomas and less often in sporadic cases. The clinical and therapeutic features ... [more ▼] Context: AIP mutations (AIPmut) give rise to a pituitary adenoma predisposition that occurs in familial isolated pituitary adenomas and less often in sporadic cases. The clinical and therapeutic features of AIPmut-associated pituitary adenomas have not been studied comprehensively. Objective: The objective of the study was to assess clinical/therapeutic characteristics of AIPmut pituitary adenomas. Design: This study was an international, multicenter, retrospective case collection/database analysis. Setting: The study was conducted at 36 tertiary referral endocrine and clinical genetics departments. Patients: Patients included 96 patients with germline AIPmut and pituitary adenomas and 232 matched AIPmut-negative acromegaly controls. Results: The AIPmut population was predominantly young and male (63.5%); first symptoms occurred as children/adolescents in 50%. At diagnosis, most tumors were macroadenomas (93.3%); extension and invasion was common. Somatotropinomas comprised 78.1% of the cohort; there were also prolactinomas (n = 13), nonsecreting adenomas (n = 7), and a TSH-secreting adenoma. AIPmut somatotropinomas were larger (P = 0.00026), with higher GH levels (P = 0.00068), more frequent extension (P = 0.018) and prolactin cosecretion (P = 0.00023), and occurred 2 decades before controls (P < 0.000001). Gigantism was more common in the AIPmut group (P < 0.000001). AIPmut somatotropinoma patients underwent more surgical interventions (P = 0.00069) and had lower decreases in GH (P = 0.00037) and IGF-I (P = 0.028) and less tumor shrinkage with somatostatin analogs (P < 0.00001) vs. controls. AIPmut prolactinomas occurred generally in young males and frequently required surgery or radiotherapy. Conclusions: AIPmut pituitary adenomas have clinical features that may negatively impact treatment efficacy. Predisposition for aggressive disease in young patients, often in a familial setting, suggests that earlier diagnosis of AIPmut pituitary adenomas may have clinical utility. [less ▲] Detailed reference viewed: 66 (33 ULg) Caractéristiques cliniques et réponses thérapeutiques des patients avec adénome hypophysaire mutés pour AIP : étude internationale sur 96 casBeckers, Albert ; Daly, Adrian ; Petrossians, Patrick et alin Annales d'Endocrinologie (2010, September), 71(5), 346 Detailed reference viewed: 12 (2 ULg) Prévalence de gastrite auto-immune et études histologiques dans une série prospective de 240 patients avec thyroïdite de HashimotoValdes Socin, Hernan Gonzalo ; Lutteri, Laurence ; Latta, Aikaterini et alin Annales d'Endocrinologie (2010, September), 71(5), 416-417 Detailed reference viewed: 49 (2 ULg) Caractéristiques des prolactinomes résistants aux agonistes dopaminergiquesVroonen, Laurent ; ; et alin Annales d'Endocrinologie (2010, September), 71(5), 347 Detailed reference viewed: 24 (3 ULg) Hypergastrinemia, parietal cell antibodies and vitamine B12 deficiency in a prospective series of 240 patients with autoimmune thyroiditis: from autoimmune gastritis to enterochomafi n cells hyperplasiaValdes Socin, Hernan Gonzalo ; Lutteri, Laurence ; Latta, Aikaterini et alin European Neuroendocrine Association - Liège, 22-25 septembre 2010 (2010, September) Detailed reference viewed: 21 (2 ULg) Liège Acromegaly Survey: Data mining in clinical research, or how to seek information vs dataPetrossians, Patrick ; Beckers, Albert ![]() in European Neuroendocrine Association - Liège, 22-25 septembre 2010 (2010, September) Detailed reference viewed: 23 (3 ULg) High prevalence of autoimmune thyroid diseases in patients with prolactinomasElenkova, Atanaska ; Petrossians, Patrick ; Beckers, Albert et alin European Neuroendocrine Association - Liège, 22-25 septembre 2010 (2010, September) Detailed reference viewed: 15 (4 ULg) ACTH silent adenoma shrinking under cabergolinePetrossians, Patrick ; Beckers, Albert ![]() in European Neuroendocrine Association - Liège, 22-25 septembre 2010 (2010, September) Detailed reference viewed: 9 (2 ULg) Liège Acromegaly Survey (LAS): First snapshotPetrossians, Patrick ; ; et alin European Neuroendocrine Association - Liège, 22-25 septembre 2010 (2010, September) Detailed reference viewed: 31 (3 ULg) Hypergastrinemia, parietal cell antibodies and vitamine B12 deficiency in a prospective series of 240 patients with autoimmune thyroiditis : from autoimmune gastritis to enterochomafin celles hyperplasiaValdes Socin, Hernan Gonzalo ; Lutteri, Laurence ; et alin European Neuroendocrine Association - Liège, 22-25 septembre 2010 (2010, September) Detailed reference viewed: 25 (6 ULg) Caractéristiques cliniques et réponses thérapeutiques des patients avec adénome hypophysaire mutés pour AIP : étude internationale sur 96 casBeckers, Albert ; Daly, Adrian ; Petrossians, Patrick et alin 27ème Congrès de la Société Française d'Endocrinologie - Deauville, 29 septembre - 2 octobre 2010 (2010, September) Detailed reference viewed: 10 (2 ULg) Comprehensive study about the characteristics of 80 dopaminergic agonist resistants prolactinomasVroonen, Laurent ; ; et alin European Neuroendocrine Association - Liège, 22-25 septembre 2010 (2010, September) Detailed reference viewed: 16 (5 ULg) Medical Treatment in Cushing’s Syndrome : Dopamine Agonists and CabergolinePetrossians, Patrick ; Thonnard, Anne-Sophie ; Beckers, Albert ![]() in Neuroendocrinology (2010), 92((supp. 1)), 116-19 Dopamine (DA) is a catecholamine with a wide range of functions and whose five subtype receptors are found in different organs where they exert a mainly inhibitory action. Since this action may also ... [more ▼] Dopamine (DA) is a catecholamine with a wide range of functions and whose five subtype receptors are found in different organs where they exert a mainly inhibitory action. Since this action may also appear in a number of secretory tumors in various locations, DA agonists have elicited some interest as a medical treatment for hypercorticism. Non-iatrogenic Cushing’s syndromes are due in 70% of the cases to a pituitary adrenocorticotropic hormone (ACTH) producing adenoma, and, less frequently, to an adrenal adenoma or an ectopic ACTH secretion by a neuroendocrine tumor. First-line treatment in Cushing’s syndrome consists of the surgical removal of the secreting tumor. However, surgery may not achieve a complete cure in a number of cases, hence emphasizing the potential benefit of a medical complementary treatment, which could also benefit patients as an alternative approach, either when waiting for, or when the patient is not eligible for surgery. Studies of corticotropic adenomas have shown that 80% of these tumors express D2 receptors. Clinical trials of DA agonists in Cushing’s disease have shown an inhibitory effect of these drugs with an inhibition of ACTH secretion and/or a decrease of tumor size. There are only a few cases of documented use of DA agonists in ectopic ACTH secretion, but when the tumor expresses DA receptors, DA agonists may represent a useful complementary treatment. DA receptors are also expressed in normal and tumoral adrenals, suggesting a potential use of DA agonists in Cushing’s syndrome secondary to adrenal tumors. However, clinical data regarding this specific situation are very scarce, maybe due to the relatively high rate of surgical cure of adrenal adenomas. In conclusion, DA agonists represent a potential preparatory or complementary treatment for endogenous Cushing’s syndrome, especially in Cushing’s disease. These compounds may be underused as suggested by the scarce number of publication and case reports in the literature. In the future, association of these drugs with somatostatin analogs may also prove beneficial. [less ▲] Detailed reference viewed: 25 (4 ULg) Clinical characteristics and therapeutic responses in patients with Germ-line AIP mutations and pituitary adenomas : An international collaborative studyDaly, Adrian ; ; Petrossians, Patrick et alin Journal of Clinical Endocrinology and Metabolism (2010), 95 Detailed reference viewed: 27 (10 ULg) Le tabac et ses effets sur le système endocrinienVALDES SOCIN, Hernan Gonzalo ; VROONEN, Laurent ; et alin Revue Médicale de Liège (2010), 65(9), 498-501 Detailed reference viewed: 7 (1 ULg) |
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