Acromegaly versus hypogonadism: bone fragility and evaluation
CONCLUSIONS: Vertebral fractures are frequent in acromegaly, and are associated with lower BMD but not with TBS. Patients with acromegaly, regardless of gonadal status, have significantly higher BMD but lower TBS than hypogonadal patients. Moreover, disease activity and hypogonadism do not influence BMD, TBS or VF in acromegaly.PMID:37689348 | DOI:10.1016/j.ando.2023.08.005 (Source: Annales d'Endocrinologie)
Source: Annales d'Endocrinologie - September 9, 2023 Category: Endocrinology Authors: Madalina Cristina Sorohan Ionela Florina Baciu Simona Andreea Galoiu Dan Alexandru Niculescu Andra Caragheorgheopol Carmen Nicoleta Iordachescu Catalina Poiana Source Type: research
Acromegaly versus hypogonadism: bone fragility and evaluation
CONCLUSIONS: Vertebral fractures are frequent in acromegaly, and are associated with lower BMD but not with TBS. Patients with acromegaly, regardless of gonadal status, have significantly higher BMD but lower TBS than hypogonadal patients. Moreover, disease activity and hypogonadism do not influence BMD, TBS or VF in acromegaly.PMID:37689348 | DOI:10.1016/j.ando.2023.08.005 (Source: Annales d'Endocrinologie)
Source: Annales d'Endocrinologie - September 9, 2023 Category: Endocrinology Authors: Madalina Cristina Sorohan Ionela Florina Baciu Simona Andreea Galoiu Dan Alexandru Niculescu Andra Caragheorgheopol Carmen Nicoleta Iordachescu Catalina Poiana Source Type: research
Autoimmune Addison's disease in the preclinical period mimics malignancy on 18F-FDG PET/CT
Ann Endocrinol (Paris). 2023 Jul 28:S0003-4266(23)00683-2. doi: 10.1016/j.ando.2023.06.005. Online ahead of print.NO ABSTRACTPMID:37679200 | DOI:10.1016/j.ando.2023.06.005 (Source: Annales d'Endocrinologie)
Source: Annales d'Endocrinologie - September 7, 2023 Category: Endocrinology Authors: Olivier Cadart Ingrid Biancheri Mounicq Dominique Lurton Capucine Bertrand H éléna Mosbah Source Type: research
Autoimmune Addison's disease in the preclinical period mimics malignancy on 18F-FDG PET/CT
Ann Endocrinol (Paris). 2023 Jul 28:S0003-4266(23)00683-2. doi: 10.1016/j.ando.2023.06.005. Online ahead of print.NO ABSTRACTPMID:37679200 | DOI:10.1016/j.ando.2023.06.005 (Source: Annales d'Endocrinologie)
Source: Annales d'Endocrinologie - September 7, 2023 Category: Endocrinology Authors: Olivier Cadart Ingrid Biancheri Mounicq Dominique Lurton Capucine Bertrand H éléna Mosbah Source Type: research
Position statement on the diagnosis and management of acromegaly: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2023 Aug 12:S0003-4266(23)00686-8. doi: 10.1016/j.ando.2023.08.003. Online ahead of print.ABSTRACTAcromegaly is a rare disease with prevalence of approximately 60 cases per million, slight female predominance and peak onset in adults in the fourth decade. Clinical diagnosis is often delayed by several years due to the slowly progressive onset of symptoms. There are multiple clinical criteria that define acromegaly: dysmorphic syndrome of insidious onset, symptoms related to the pituitary tumor (headaches, visual disorders), general signs (sweating, carpal tunnel syndrome, joint pain, etc.), complica...
Source: Annales d'Endocrinologie - August 14, 2023 Category: Endocrinology Authors: Thierry Brue Ha ïfa Rahabi Abdoulaye Barry Anne Barlier J érôme Bertherat Fran çoise Borson-Chazot Fr édéric Castinetti Laure Cazabat Olivier Chabre Nicolas Chevalier Sophie Christin-Maitre Christine Cortet Delphine Drui Peter Kamenicky Catherine La Source Type: research
Position statement on the diagnosis and management of acromegaly: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2023 Aug 12:S0003-4266(23)00686-8. doi: 10.1016/j.ando.2023.08.003. Online ahead of print.ABSTRACTAcromegaly is a rare disease with prevalence of approximately 60 cases per million, slight female predominance and peak onset in adults in the fourth decade. Clinical diagnosis is often delayed by several years due to the slowly progressive onset of symptoms. There are multiple clinical criteria that define acromegaly: dysmorphic syndrome of insidious onset, symptoms related to the pituitary tumor (headaches, visual disorders), general signs (sweating, carpal tunnel syndrome, joint pain, etc.), complica...
Source: Annales d'Endocrinologie - August 14, 2023 Category: Endocrinology Authors: Thierry Brue Ha ïfa Rahabi Abdoulaye Barry Anne Barlier J érôme Bertherat Fran çoise Borson-Chazot Fr édéric Castinetti Laure Cazabat Olivier Chabre Nicolas Chevalier Sophie Christin-Maitre Christine Cortet Delphine Drui Peter Kamenicky Catherine La Source Type: research
Position statement on the diagnosis and management of acromegaly: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2023 Aug 12:S0003-4266(23)00686-8. doi: 10.1016/j.ando.2023.08.003. Online ahead of print.ABSTRACTAcromegaly is a rare disease with prevalence of approximately 60 cases per million, slight female predominance and peak onset in adults in the fourth decade. Clinical diagnosis is often delayed by several years due to the slowly progressive onset of symptoms. There are multiple clinical criteria that define acromegaly: dysmorphic syndrome of insidious onset, symptoms related to the pituitary tumor (headaches, visual disorders), general signs (sweating, carpal tunnel syndrome, joint pain, etc.), complica...
Source: Annales d'Endocrinologie - August 14, 2023 Category: Endocrinology Authors: Thierry Brue Ha ïfa Rahabi Abdoulaye Barry Anne Barlier J érôme Bertherat Fran çoise Borson-Chazot Fr édéric Castinetti Laure Cazabat Olivier Chabre Nicolas Chevalier Sophie Christin-Maitre Christine Cortet Delphine Drui Peter Kamenicky Catherine La Source Type: research
Position statement on the diagnosis and management of acromegaly: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2023 Aug 12:S0003-4266(23)00686-8. doi: 10.1016/j.ando.2023.08.003. Online ahead of print.ABSTRACTAcromegaly is a rare disease with prevalence of approximately 60 cases per million, slight female predominance and peak onset in adults in the fourth decade. Clinical diagnosis is often delayed by several years due to the slowly progressive onset of symptoms. There are multiple clinical criteria that define acromegaly: dysmorphic syndrome of insidious onset, symptoms related to the pituitary tumor (headaches, visual disorders), general signs (sweating, carpal tunnel syndrome, joint pain, etc.), complica...
Source: Annales d'Endocrinologie - August 14, 2023 Category: Endocrinology Authors: Thierry Brue Ha ïfa Rahabi Abdoulaye Barry Anne Barlier J érôme Bertherat Fran çoise Borson-Chazot Fr édéric Castinetti Laure Cazabat Olivier Chabre Nicolas Chevalier Sophie Christin-Maitre Christine Cortet Delphine Drui Peter Kamenicky Catherine La Source Type: research
Position statement on the diagnosis and management of acromegaly: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2023 Aug 12:S0003-4266(23)00686-8. doi: 10.1016/j.ando.2023.08.003. Online ahead of print.ABSTRACTAcromegaly is a rare disease with prevalence of approximately 60 cases per million, slight female predominance and peak onset in adults in the fourth decade. Clinical diagnosis is often delayed by several years due to the slowly progressive onset of symptoms. There are multiple clinical criteria that define acromegaly: dysmorphic syndrome of insidious onset, symptoms related to the pituitary tumor (headaches, visual disorders), general signs (sweating, carpal tunnel syndrome, joint pain, etc.), complica...
Source: Annales d'Endocrinologie - August 14, 2023 Category: Endocrinology Authors: Thierry Brue Ha ïfa Rahabi Abdoulaye Barry Anne Barlier J érôme Bertherat Fran çoise Borson-Chazot Fr édéric Castinetti Laure Cazabat Olivier Chabre Nicolas Chevalier Sophie Christin-Maitre Christine Cortet Delphine Drui Peter Kamenicky Catherine La Source Type: research
Position statement on the diagnosis and management of acromegaly: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2023 Aug 12:S0003-4266(23)00686-8. doi: 10.1016/j.ando.2023.08.003. Online ahead of print.ABSTRACTAcromegaly is a rare disease with prevalence of approximately 60 cases per million, slight female predominance and peak onset in adults in the fourth decade. Clinical diagnosis is often delayed by several years due to the slowly progressive onset of symptoms. There are multiple clinical criteria that define acromegaly: dysmorphic syndrome of insidious onset, symptoms related to the pituitary tumor (headaches, visual disorders), general signs (sweating, carpal tunnel syndrome, joint pain, etc.), complica...
Source: Annales d'Endocrinologie - August 14, 2023 Category: Endocrinology Authors: Thierry Brue Ha ïfa Rahabi Abdoulaye Barry Anne Barlier J érôme Bertherat Fran çoise Borson-Chazot Fr édéric Castinetti Laure Cazabat Olivier Chabre Nicolas Chevalier Sophie Christin-Maitre Christine Cortet Delphine Drui Peter Kamenicky Catherine La Source Type: research
Position statement on the diagnosis and management of acromegaly: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2023 Aug 12:S0003-4266(23)00686-8. doi: 10.1016/j.ando.2023.08.003. Online ahead of print.ABSTRACTAcromegaly is a rare disease with prevalence of approximately 60 cases per million, slight female predominance and peak onset in adults in the fourth decade. Clinical diagnosis is often delayed by several years due to the slowly progressive onset of symptoms. There are multiple clinical criteria that define acromegaly: dysmorphic syndrome of insidious onset, symptoms related to the pituitary tumor (headaches, visual disorders), general signs (sweating, carpal tunnel syndrome, joint pain, etc.), complica...
Source: Annales d'Endocrinologie - August 14, 2023 Category: Endocrinology Authors: Thierry Brue Ha ïfa Rahabi Abdoulaye Barry Anne Barlier J érôme Bertherat Fran çoise Borson-Chazot Fr édéric Castinetti Laure Cazabat Olivier Chabre Nicolas Chevalier Sophie Christin-Maitre Christine Cortet Delphine Drui Peter Kamenicky Catherine La Source Type: research
Position statement on the diagnosis and management of acromegaly: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2023 Aug 12:S0003-4266(23)00686-8. doi: 10.1016/j.ando.2023.08.003. Online ahead of print.ABSTRACTAcromegaly is a rare disease with prevalence of approximately 60 cases per million, slight female predominance and peak onset in adults in the fourth decade. Clinical diagnosis is often delayed by several years due to the slowly progressive onset of symptoms. There are multiple clinical criteria that define acromegaly: dysmorphic syndrome of insidious onset, symptoms related to the pituitary tumor (headaches, visual disorders), general signs (sweating, carpal tunnel syndrome, joint pain, etc.), complica...
Source: Annales d'Endocrinologie - August 14, 2023 Category: Endocrinology Authors: Thierry Brue Ha ïfa Rahabi Abdoulaye Barry Anne Barlier J érôme Bertherat Fran çoise Borson-Chazot Fr édéric Castinetti Laure Cazabat Olivier Chabre Nicolas Chevalier Sophie Christin-Maitre Christine Cortet Delphine Drui Peter Kamenicky Catherine La Source Type: research
Position statement on the diagnosis and management of acromegaly: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2023 Aug 12:S0003-4266(23)00686-8. doi: 10.1016/j.ando.2023.08.003. Online ahead of print.ABSTRACTAcromegaly is a rare disease with prevalence of approximately 60 cases per million, slight female predominance and peak onset in adults in the fourth decade. Clinical diagnosis is often delayed by several years due to the slowly progressive onset of symptoms. There are multiple clinical criteria that define acromegaly: dysmorphic syndrome of insidious onset, symptoms related to the pituitary tumor (headaches, visual disorders), general signs (sweating, carpal tunnel syndrome, joint pain, etc.), complica...
Source: Annales d'Endocrinologie - August 14, 2023 Category: Endocrinology Authors: Thierry Brue Ha ïfa Rahabi Abdoulaye Barry Anne Barlier J érôme Bertherat Fran çoise Borson-Chazot Fr édéric Castinetti Laure Cazabat Olivier Chabre Nicolas Chevalier Sophie Christin-Maitre Christine Cortet Delphine Drui Peter Kamenicky Catherine La Source Type: research
Position statement on the diagnosis and management of acromegaly: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2023 Aug 12:S0003-4266(23)00686-8. doi: 10.1016/j.ando.2023.08.003. Online ahead of print.ABSTRACTAcromegaly is a rare disease with prevalence of approximately 60 cases per million, slight female predominance and peak onset in adults in the fourth decade. Clinical diagnosis is often delayed by several years due to the slowly progressive onset of symptoms. There are multiple clinical criteria that define acromegaly: dysmorphic syndrome of insidious onset, symptoms related to the pituitary tumor (headaches, visual disorders), general signs (sweating, carpal tunnel syndrome, joint pain, etc.), complica...
Source: Annales d'Endocrinologie - August 14, 2023 Category: Endocrinology Authors: Thierry Brue Ha ïfa Rahabi Abdoulaye Barry Anne Barlier J érôme Bertherat Fran çoise Borson-Chazot Fr édéric Castinetti Laure Cazabat Olivier Chabre Nicolas Chevalier Sophie Christin-Maitre Christine Cortet Delphine Drui Peter Kamenicky Catherine La Source Type: research
Position statement on the diagnosis and management of acromegaly: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2023 Aug 12:S0003-4266(23)00686-8. doi: 10.1016/j.ando.2023.08.003. Online ahead of print.ABSTRACTAcromegaly is a rare disease with prevalence of approximately 60 cases per million, slight female predominance and peak onset in adults in the fourth decade. Clinical diagnosis is often delayed by several years due to the slowly progressive onset of symptoms. There are multiple clinical criteria that define acromegaly: dysmorphic syndrome of insidious onset, symptoms related to the pituitary tumor (headaches, visual disorders), general signs (sweating, carpal tunnel syndrome, joint pain, etc.), complica...
Source: Annales d'Endocrinologie - August 14, 2023 Category: Endocrinology Authors: Thierry Brue Ha ïfa Rahabi Abdoulaye Barry Anne Barlier J érôme Bertherat Fran çoise Borson-Chazot Fr édéric Castinetti Laure Cazabat Olivier Chabre Nicolas Chevalier Sophie Christin-Maitre Christine Cortet Delphine Drui Peter Kamenicky Catherine La Source Type: research
