All Relations between Acromegaly and gh

Publication Sentence Publish Date Extraction Date Species
Iulia Potorac, Jean-François Bonneville, Adrian F Daly, Wouter de Herder, Patricia Fainstein-Day, Philippe Chanson, Marta Korbonits, Fernando Cordido, Elisa Baranski Lamback, Mohamed Abid, Véronique Raverot, Gerald Raverot, Emma Anda Apiñániz, Philippe Caron, Helene Du Boullay, Martin Bildingmaier, Marek Bolanowski, Marie Laloi-Michelin, Francoise Borson-Chazot, Olivier Chabre, Sophie Christin-Maitre, Claire Briet, Gonzalo Diaz-Soto, Fabrice Bonneville, Frederic Castinetti, Mônica R Gadelha, Nathalie Oliveira Santana, Maria Stelmachowska-Banaś, Tomas Gudbjartsson, Roció Villar-Taibo, Taiba Zornitzki, Luaba Tshibanda, Patrick Petrossians, Albert Becker. Pituitary MRI Features in Acromegaly due to Ectopic GHRH Secretion from a Neuroendocrine Tumor: Analysis of 30 cases. The Journal of clinical endocrinology and metabolism. 2022-05-05. PMID:35512251. identifying the underlying cause for the gh hypersecretion in the setting of ectopic ghrh excess is, however, essential for proper management both of acromegaly and the net. 2022-05-05 2023-08-13 Not clear
Isabel Inacio, Liliana Fonseca, Ana Amado, Vania Benido, Isabel Ribeiro, Jorge Dores, Claudia Amaral, Maria Helena Cardos. Characteristics and treatment outcomes of micromegaly - acromegaly with apparently normal basal GH: A retrospective study and literature review. Endocrine regulations. vol 56. issue 2. 2022-04-30. PMID:35489048. characteristics and treatment outcomes of micromegaly - acromegaly with apparently normal basal gh: a retrospective study and literature review. 2022-04-30 2023-08-13 Not clear
Rosa Maria Paragliola, Cinzia Carrozza, Salvatore M Corsello, Roberto Salvator. The biochemical diagnosis of acromegaly: revising the role of measurement of IGF-I and GH after glucose load in 5 questions. Expert review of endocrinology & metabolism. 2022-04-29. PMID:35485763. the biochemical diagnosis of acromegaly: revising the role of measurement of igf-i and gh after glucose load in 5 questions. 2022-04-29 2023-08-13 Not clear
Rosa Maria Paragliola, Cinzia Carrozza, Salvatore M Corsello, Roberto Salvator. The biochemical diagnosis of acromegaly: revising the role of measurement of IGF-I and GH after glucose load in 5 questions. Expert review of endocrinology & metabolism. 2022-04-29. PMID:35485763. acromegaly is a rare disorder characterized by the excessive secretion of growth hormone (gh), mostly caused by pituitary adenomas. 2022-04-29 2023-08-13 Not clear
Jakob Dal, Christian Rosendal, Jesper Karmisholt, Ulla Feldt-Rasmussen, Marianne Andersen, Marianne Klose, Claus Feldttoft, Ansgar Heck, Eigil H Nielsen, Jens O L Jørgense. Sex difference in patients with controlled acromegaly - a multicenter survey. Clinical endocrinology. 2022-04-27. PMID:35474467. active acromegaly is subject to sex differences in gh and igf-i patterns as well as clinical features but whether this also pertains to controlled disease is unclear. 2022-04-27 2023-08-13 human
Jiwon Kim, Yoon-A Hwang, Yae Won Park, Ju Hyung Moon, Eui Hyun Kim, Jae Won Hong, Eun Jig Lee, Cheol Ryong K. Revisiting growth hormone nadir cut-offs for remission in patients with acromegaly. European journal of endocrinology. vol 186. issue 6. 2022-04-26. PMID:35380987. over the past decade, the growth hormone (gh) nadir cut-off during the oral glucose tolerance test for remission in patients with acromegaly was changed from 0.4 to 1.0 μg/l due to the limited use of ultrasensitive detection kits to measure gh levels. 2022-04-26 2023-08-16 Not clear
Jiwon Kim, Yoon-A Hwang, Yae Won Park, Ju Hyung Moon, Eui Hyun Kim, Jae Won Hong, Eun Jig Lee, Cheol Ryong K. Revisiting growth hormone nadir cut-offs for remission in patients with acromegaly. European journal of endocrinology. vol 186. issue 6. 2022-04-26. PMID:35380987. this retrospective study aimed to investigate the association between different gh nadir cut-offs and prognosis in patients with acromegaly. 2022-04-26 2023-08-16 Not clear
Kevin C J Yuen, Susan L Samso. Oral Octreotide: A Review of Recent Clinical Trials and Practical Recommendations for Its Use in the Treatment of Patients With Acromegaly. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists. 2022-04-22. PMID:35452815. acromegaly is characterized by chronic growth hormone (gh) and insulin-like growth factor-i (igf-i) hypersecretion, often caused by a gh-secreting pituitary adenoma. 2022-04-22 2023-08-13 Not clear
Gianmaria Salvio, Marianna Martino, Giancarlo Balercia, Giorgio Arnald. Acromegaly and male sexual health. Reviews in endocrine & metabolic disorders. 2022-04-02. PMID:35364803. acromegaly is a rare pathology characterized by chronic hypersecretion of growth hormone (gh) and insulin-like growth factor-1 (igf-1) that causes somatic, metabolic, and systemic changes. 2022-04-02 2023-08-13 Not clear
Gianmaria Salvio, Marianna Martino, Giancarlo Balercia, Giorgio Arnald. Acromegaly and male sexual health. Reviews in endocrine & metabolic disorders. 2022-04-02. PMID:35364803. moreover, hypogonadism is also one of the factors linking acromegaly to erectile dysfunction (ed), but also metabolic complications of acromegaly and, probably, gh itself contribute to the genesis of this disorder. 2022-04-02 2023-08-13 Not clear
Stefano Frara, Meliha Melin Uygur, Luigi di Filippo, Mauro Doga, Marco Losa, Simona Santoro, Pietro Mortini, Andrea Giustin. High Prevalence of Vertebral Fractures Associated with Preoperative GH Levels in Patients with recent Diagnosis of Acromegaly. The Journal of clinical endocrinology and metabolism. 2022-03-29. PMID:35349698. high prevalence of vertebral fractures associated with preoperative gh levels in patients with recent diagnosis of acromegaly. 2022-03-29 2023-08-13 Not clear
Gherardo Mazziotti, Andrea G Lania, Ernesto Canali. Skeletal disorders associated with the growth hormone-insulin-like growth factor 1 axis. Nature reviews. Endocrinology. 2022-03-15. PMID:35288658. the consequence is an increased risk of fractures in individuals with ghd or acromegaly, a condition of gh excess. 2022-03-15 2023-08-13 human
Anna Bogusławska, Aleksandra Gilis-Januszewska, Magdalena Godlewska, Andrzej Nowak, Jerzy Starzyk, Alicja Hubalewska-Dydejczy. Gender and age differences among patients with acromegaly. Polish archives of internal medicine. 2022-03-15. PMID:35289160. acromegaly is a chronic, slowly progressive disorder caused mostly by growth hormone (gh) -producing pituitary neuroendocrine tumors (pitnets). 2022-03-15 2023-08-13 Not clear
E E Sakhnova, E G Przhiyalkovskaya, Zh E Belaya, G A Melnichenk. [Discordant parameters of insulin-like growth factor 1 and growth hormone in the diagnosis and monitoring of acromegaly]. Problemy endokrinologii. vol 68. issue 1. 2022-03-09. PMID:35262296. the tests for the diagnosis of acromegaly are measurement of both serum gh, and gh after oral glucose administration; serum insulin-like growth factor-1 (igf-1). 2022-03-09 2023-08-13 Not clear
E E Sakhnova, E G Przhiyalkovskaya, Zh E Belaya, G A Melnichenk. [Discordant parameters of insulin-like growth factor 1 and growth hormone in the diagnosis and monitoring of acromegaly]. Problemy endokrinologii. vol 68. issue 1. 2022-03-09. PMID:35262296. this review discusses the prevalence of discordant gh and igf-1 outcomes in patients with acromegaly; factors causing this discrepancy; the impact of hormone levels on treatment outcomes. 2022-03-09 2023-08-13 Not clear
Ravi Sonkar, Ryan Berry, Mary N Latimer, Sumanth D Prabhu, Martin E Young, Stuart J Fran. Augmented Cardiac Growth Hormone Signaling Contributes to Cardiomyopathy Following Genetic Disruption of the Cardiomyocyte Circadian Clock. Frontiers in pharmacology. vol 13. 2022-03-07. PMID:35250583. gh acts in part through induction of insulin-like growth factor 1 (igf1), and excess gh/igf1 signaling has been linked to pathologies such as insulin resistance, acromegaly, and cardiomyopathy. 2022-03-07 2023-08-13 mouse
Joan Gil, Montserrat Marques-Pamies, Elena Valassi, Araceli García-Martínez, Guillermo Serra, Cristina Hostalot, Carmen Fajardo-Montañana, Cristina Carrato, Ignacio Bernabeu, Mónica Marazuela, Helena Rodríguez-Lloveras, Rosa Cámara, Isabel Salinas, Cristina Lamas, Betina Biagetti, Andreu Simó-Servat, Susan M Webb, Antonio Picó, Mireia Jordà, Manel Puig-Doming. Implications of Heterogeneity of Epithelial-Mesenchymal States in Acromegaly Therapeutic Pharmacologic Response. Biomedicines. vol 10. issue 2. 2022-02-25. PMID:35203668. acromegaly is caused by excess growth hormone (gh) produced by a pituitary tumor. 2022-02-25 2023-08-13 Not clear
T Bonora, E Rigamonti, M Capoferri, M L De Pern. Acromegalic cardiomyopathy: a neglected cause of cardiomyopathy. La Clinica terapeutica. vol 173. issue 1. 2022-02-11. PMID:35147643. acromegaly represents a rare endocrine condition characterized by an excessive secretion of the growth hormone (gh) and the insulin-like growth factor-1 (igf-1), mostly subsequent to a pituitary adenoma. 2022-02-11 2023-08-13 Not clear
Eva C Coopmans, Aart J van der Lely, Sebastian J C M M Negger. Approach to the patient with treatment resistant acromegaly. The Journal of clinical endocrinology and metabolism. 2022-01-28. PMID:35090028. acromegaly, if left untreated, is a rare and chronic disorder, commonly caused by a growth hormone (gh)-producing pituitary adenoma and is associated with significant comorbidities and an increased mortality. 2022-01-28 2023-08-13 Not clear
Akira Taguchi, Yasuyuki Kinoshita, Atsushi Tominaga, Vishwa Jeet Amatya, Yukio Takeshima, Fumiyuki Yamasak. Metachronous Double Pituitary Adenoma with Altered Transcriptional Factor Profile: A Case Report and Literature Review. NMC case report journal. vol 8. issue 1. 2022-01-26. PMID:35079531. the endocrine evaluation confirmed acromegaly because of high serum levels of igf-1 and insufficient suppression of gh levels upon ogtt. 2022-01-26 2023-08-13 Not clear