Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis

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Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis. / Ljubicic, Marie Lindhardt; Jørgensen, Anne; Acerini, Carlo; Andrade, Juliana; Balsamo, Antonio; Bertelloni, Silvano; Cools, Martine; Cuccaro, Rieko Tadokoro; Darendeliler, Feyza; Flück, Christa E; Grinspon, Romina P; Maciel-Guerra, Andrea; Guran, Tulay; Hannema, Sabine E; Lucas-Herald, Angela K; Hiort, Olaf; Holterhus, Paul Martin; Lichiardopol, Corina; Looijenga, Leendert H J; Ortolano, Rita; Riedl, Stefan; Ahmed, S Faisal; Juul, Anders.

I: The Journal of clinical endocrinology and metabolism, Bind 104, Nr. 10, 2019, s. 4366-4381.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ljubicic, ML, Jørgensen, A, Acerini, C, Andrade, J, Balsamo, A, Bertelloni, S, Cools, M, Cuccaro, RT, Darendeliler, F, Flück, CE, Grinspon, RP, Maciel-Guerra, A, Guran, T, Hannema, SE, Lucas-Herald, AK, Hiort, O, Holterhus, PM, Lichiardopol, C, Looijenga, LHJ, Ortolano, R, Riedl, S, Ahmed, SF & Juul, A 2019, 'Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis', The Journal of clinical endocrinology and metabolism, bind 104, nr. 10, s. 4366-4381. https://doi.org/10.1210/jc.2018-02752

APA

Ljubicic, M. L., Jørgensen, A., Acerini, C., Andrade, J., Balsamo, A., Bertelloni, S., Cools, M., Cuccaro, R. T., Darendeliler, F., Flück, C. E., Grinspon, R. P., Maciel-Guerra, A., Guran, T., Hannema, S. E., Lucas-Herald, A. K., Hiort, O., Holterhus, P. M., Lichiardopol, C., Looijenga, L. H. J., ... Juul, A. (2019). Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis. The Journal of clinical endocrinology and metabolism, 104(10), 4366-4381. https://doi.org/10.1210/jc.2018-02752

Vancouver

Ljubicic ML, Jørgensen A, Acerini C, Andrade J, Balsamo A, Bertelloni S o.a. Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis. The Journal of clinical endocrinology and metabolism. 2019;104(10):4366-4381. https://doi.org/10.1210/jc.2018-02752

Author

Ljubicic, Marie Lindhardt ; Jørgensen, Anne ; Acerini, Carlo ; Andrade, Juliana ; Balsamo, Antonio ; Bertelloni, Silvano ; Cools, Martine ; Cuccaro, Rieko Tadokoro ; Darendeliler, Feyza ; Flück, Christa E ; Grinspon, Romina P ; Maciel-Guerra, Andrea ; Guran, Tulay ; Hannema, Sabine E ; Lucas-Herald, Angela K ; Hiort, Olaf ; Holterhus, Paul Martin ; Lichiardopol, Corina ; Looijenga, Leendert H J ; Ortolano, Rita ; Riedl, Stefan ; Ahmed, S Faisal ; Juul, Anders. / Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis. I: The Journal of clinical endocrinology and metabolism. 2019 ; Bind 104, Nr. 10. s. 4366-4381.

Bibtex

@article{ed2a1f7ea7304f3882b1054fd1ece0ac,
title = "Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis",
abstract = "CONTEXT: Larger studies on outcomes in males with 45,X/46,XY mosaicism are rare.OBJECTIVE: To compare health outcomes in males with 45,X/46,XY diagnosed as a result of either genital abnormalities at birth or nongenital reasons later in life.DESIGN: A retrospective, multicenter study.SETTING: Sixteen tertiary centers.PATIENTS OR OTHER PARTICIPANTS: Sixty-three males older than 13 years with 45,X/46,XY mosaicism.MAIN OUTCOME MEASURES: Health outcomes, such as genital phenotype, gonadal function, growth, comorbidities, fertility, and gonadal histology, including risk of neoplasia.RESULTS: Thirty-five patients were in the genital group and 28 in the nongenital. Eighty percent of all patients experienced spontaneous pubertal onset, significantly more in the nongenital group (P = 0.023). Patients were significantly shorter in the genital group with median adult heights of 156.7 cm and 164.5 cm, respectively (P = 0.016). Twenty-seven percent of patients received recombinant human GH. Forty-four patients had gonadal histology evaluated. Germ cells were detected in 42%. Neoplasia in situ was found in five patients. Twenty-five percent had focal spermatogenesis, and another 25.0% had arrested spermatogenesis. Fourteen out of 17 (82%) with semen analyses were azoospermic; three had motile sperm.CONCLUSION: Patients diagnosed as a result of genital abnormalities have poorer health outcomes than those diagnosed as a result of nongenital reasons. Most patients, however, have relatively good endocrine gonadal function, but most are also short statured. Patients have a risk of gonadal neoplasia, and most are azoospermic, but almost one-half of patients has germ cells present histologically and up to one-quarter has focal spermatogenesis, providing hope for fertility treatment options.",
author = "Ljubicic, {Marie Lindhardt} and Anne J{\o}rgensen and Carlo Acerini and Juliana Andrade and Antonio Balsamo and Silvano Bertelloni and Martine Cools and Cuccaro, {Rieko Tadokoro} and Feyza Darendeliler and Fl{\"u}ck, {Christa E} and Grinspon, {Romina P} and Andrea Maciel-Guerra and Tulay Guran and Hannema, {Sabine E} and Lucas-Herald, {Angela K} and Olaf Hiort and Holterhus, {Paul Martin} and Corina Lichiardopol and Looijenga, {Leendert H J} and Rita Ortolano and Stefan Riedl and Ahmed, {S Faisal} and Anders Juul",
note = "Copyright {\textcopyright} 2019 Endocrine Society.",
year = "2019",
doi = "10.1210/jc.2018-02752",
language = "English",
volume = "104",
pages = "4366--4381",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0021-972X",
publisher = "Oxford University Press",
number = "10",

}

RIS

TY - JOUR

T1 - Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis

AU - Ljubicic, Marie Lindhardt

AU - Jørgensen, Anne

AU - Acerini, Carlo

AU - Andrade, Juliana

AU - Balsamo, Antonio

AU - Bertelloni, Silvano

AU - Cools, Martine

AU - Cuccaro, Rieko Tadokoro

AU - Darendeliler, Feyza

AU - Flück, Christa E

AU - Grinspon, Romina P

AU - Maciel-Guerra, Andrea

AU - Guran, Tulay

AU - Hannema, Sabine E

AU - Lucas-Herald, Angela K

AU - Hiort, Olaf

AU - Holterhus, Paul Martin

AU - Lichiardopol, Corina

AU - Looijenga, Leendert H J

AU - Ortolano, Rita

AU - Riedl, Stefan

AU - Ahmed, S Faisal

AU - Juul, Anders

N1 - Copyright © 2019 Endocrine Society.

PY - 2019

Y1 - 2019

N2 - CONTEXT: Larger studies on outcomes in males with 45,X/46,XY mosaicism are rare.OBJECTIVE: To compare health outcomes in males with 45,X/46,XY diagnosed as a result of either genital abnormalities at birth or nongenital reasons later in life.DESIGN: A retrospective, multicenter study.SETTING: Sixteen tertiary centers.PATIENTS OR OTHER PARTICIPANTS: Sixty-three males older than 13 years with 45,X/46,XY mosaicism.MAIN OUTCOME MEASURES: Health outcomes, such as genital phenotype, gonadal function, growth, comorbidities, fertility, and gonadal histology, including risk of neoplasia.RESULTS: Thirty-five patients were in the genital group and 28 in the nongenital. Eighty percent of all patients experienced spontaneous pubertal onset, significantly more in the nongenital group (P = 0.023). Patients were significantly shorter in the genital group with median adult heights of 156.7 cm and 164.5 cm, respectively (P = 0.016). Twenty-seven percent of patients received recombinant human GH. Forty-four patients had gonadal histology evaluated. Germ cells were detected in 42%. Neoplasia in situ was found in five patients. Twenty-five percent had focal spermatogenesis, and another 25.0% had arrested spermatogenesis. Fourteen out of 17 (82%) with semen analyses were azoospermic; three had motile sperm.CONCLUSION: Patients diagnosed as a result of genital abnormalities have poorer health outcomes than those diagnosed as a result of nongenital reasons. Most patients, however, have relatively good endocrine gonadal function, but most are also short statured. Patients have a risk of gonadal neoplasia, and most are azoospermic, but almost one-half of patients has germ cells present histologically and up to one-quarter has focal spermatogenesis, providing hope for fertility treatment options.

AB - CONTEXT: Larger studies on outcomes in males with 45,X/46,XY mosaicism are rare.OBJECTIVE: To compare health outcomes in males with 45,X/46,XY diagnosed as a result of either genital abnormalities at birth or nongenital reasons later in life.DESIGN: A retrospective, multicenter study.SETTING: Sixteen tertiary centers.PATIENTS OR OTHER PARTICIPANTS: Sixty-three males older than 13 years with 45,X/46,XY mosaicism.MAIN OUTCOME MEASURES: Health outcomes, such as genital phenotype, gonadal function, growth, comorbidities, fertility, and gonadal histology, including risk of neoplasia.RESULTS: Thirty-five patients were in the genital group and 28 in the nongenital. Eighty percent of all patients experienced spontaneous pubertal onset, significantly more in the nongenital group (P = 0.023). Patients were significantly shorter in the genital group with median adult heights of 156.7 cm and 164.5 cm, respectively (P = 0.016). Twenty-seven percent of patients received recombinant human GH. Forty-four patients had gonadal histology evaluated. Germ cells were detected in 42%. Neoplasia in situ was found in five patients. Twenty-five percent had focal spermatogenesis, and another 25.0% had arrested spermatogenesis. Fourteen out of 17 (82%) with semen analyses were azoospermic; three had motile sperm.CONCLUSION: Patients diagnosed as a result of genital abnormalities have poorer health outcomes than those diagnosed as a result of nongenital reasons. Most patients, however, have relatively good endocrine gonadal function, but most are also short statured. Patients have a risk of gonadal neoplasia, and most are azoospermic, but almost one-half of patients has germ cells present histologically and up to one-quarter has focal spermatogenesis, providing hope for fertility treatment options.

U2 - 10.1210/jc.2018-02752

DO - 10.1210/jc.2018-02752

M3 - Journal article

C2 - 31127831

VL - 104

SP - 4366

EP - 4381

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 10

ER -

ID: 228855634