Outcomes of SDHB Pathogenic Variant Carriers.
- Publisher:
- The Endocrine Society
- Publication Type:
- Journal Article
- Citation:
- J Clin Endocrinol Metab, 2024, 109, (9), pp. 2400-2410
- Issue Date:
- 2024-08-13
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Field | Value | Language |
---|---|---|
dc.contributor.author | Davidoff, DF | |
dc.contributor.author |
De Abreu Lourenco, R https://orcid.org/0000-0002-5978-8774 |
|
dc.contributor.author | Tsang, VHM | |
dc.contributor.author | Benn, DE | |
dc.contributor.author | Clifton-Bligh, RJ | |
dc.date.accessioned | 2024-11-19T03:45:23Z | |
dc.date.available | 2024-11-19T03:45:23Z | |
dc.date.issued | 2024-08-13 | |
dc.identifier.citation | J Clin Endocrinol Metab, 2024, 109, (9), pp. 2400-2410 | |
dc.identifier.issn | 0021-972X | |
dc.identifier.issn | 1945-7197 | |
dc.identifier.uri | http://hdl.handle.net/10453/181984 | |
dc.description.abstract | CONTEXT: Carriers of germline pathogenic variants (PVs) in succinate dehydrogenase type B (SDHB) are at increased risk of developing pheochromocytomas and paragangliomas (PPGLs). Understanding their outcomes can guide recommendations for risk assessment and early detection. OBJECTIVE: We performed a systematic review and meta-analysis of the following outcomes in SDHB PV carriers: age-specific risk of developing tumors, metastatic progression, second primary tumor development, and mortality. METHODS: PubMed, MEDLINE, and EMBASE were searched. Sixteen studies met the inclusion criteria and were sorted into 4 outcome categories: age-specific penetrance, metastatic disease, risk of second tumor, and mortality. We assessed heterogeneity and performed a meta-analysis across studies using a random-effects model with the DerSimonian and Laird method. RESULTS: Penetrance of PPGLs for nonproband/nonindex SDHB PV carriers by age 20 was 4% (95% CI, 3%-6%), 11% (95% CI, 8%-15%) by age 40, 24% (95% CI, 19%-31%) by age 60%, and 35% (95% CI, 25%-47%) by age 80. The overall risk of metastatic disease for nonproband/nonindex carriers with PPGLs was 9% (95%, CI 5%-16%) per lifetime. In all affected cases (combining both proband/index and nonproband/nonindex carriers with tumors), the risk of a second tumor was 24% (95% CI, 18%-31%) and all-cause 5-year mortality was 18% (95% CI, 6%-40%). CONCLUSION: Penetrance for PPGLs in SDHB PV carriers increases linearly with age. Affected carriers are at risk of developing and dying of metastatic disease, or of developing second tumors. Lifelong surveillance is appropriate. | |
dc.format | ||
dc.language | eng | |
dc.publisher | The Endocrine Society | |
dc.relation.ispartof | J Clin Endocrinol Metab | |
dc.relation.isbasedon | 10.1210/clinem/dgae233 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 1103 Clinical Sciences, 1114 Paediatrics and Reproductive Medicine | |
dc.subject.classification | Endocrinology & Metabolism | |
dc.subject.classification | 3202 Clinical sciences | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Succinate Dehydrogenase | |
dc.subject.mesh | Paraganglioma | |
dc.subject.mesh | Adrenal Gland Neoplasms | |
dc.subject.mesh | Pheochromocytoma | |
dc.subject.mesh | Penetrance | |
dc.subject.mesh | Germ-Line Mutation | |
dc.subject.mesh | Heterozygote | |
dc.subject.mesh | Genetic Predisposition to Disease | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Paraganglioma | |
dc.subject.mesh | Pheochromocytoma | |
dc.subject.mesh | Adrenal Gland Neoplasms | |
dc.subject.mesh | Genetic Predisposition to Disease | |
dc.subject.mesh | Succinate Dehydrogenase | |
dc.subject.mesh | Heterozygote | |
dc.subject.mesh | Penetrance | |
dc.subject.mesh | Germ-Line Mutation | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Succinate Dehydrogenase | |
dc.subject.mesh | Paraganglioma | |
dc.subject.mesh | Adrenal Gland Neoplasms | |
dc.subject.mesh | Pheochromocytoma | |
dc.subject.mesh | Penetrance | |
dc.subject.mesh | Germ-Line Mutation | |
dc.subject.mesh | Heterozygote | |
dc.subject.mesh | Genetic Predisposition to Disease | |
dc.title | Outcomes of SDHB Pathogenic Variant Carriers. | |
dc.type | Journal Article | |
utslib.citation.volume | 109 | |
utslib.location.activity | United States | |
utslib.for | 1103 Clinical Sciences | |
utslib.for | 1114 Paediatrics and Reproductive Medicine | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Health | |
pubs.organisational-group | University of Technology Sydney/UTS Groups | |
pubs.organisational-group | University of Technology Sydney/UTS Groups/INSIGHT: Institute for Innovative Solutions for Well-being and Health/Centre for Health Economics Research and Evaluation (CHERE) | |
pubs.organisational-group | University of Technology Sydney/UTS Groups/INSIGHT: Institute for Innovative Solutions for Well-being and Health | |
pubs.organisational-group | University of Technology Sydney/UTS Groups/Centre for Health Technologies (CHT) | |
utslib.copyright.status | open_access | * |
dc.rights.license | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.date.updated | 2024-11-19T03:45:21Z | |
pubs.issue | 9 | |
pubs.publication-status | Published | |
pubs.volume | 109 | |
utslib.citation.issue | 9 |
Abstract:
CONTEXT: Carriers of germline pathogenic variants (PVs) in succinate dehydrogenase type B (SDHB) are at increased risk of developing pheochromocytomas and paragangliomas (PPGLs). Understanding their outcomes can guide recommendations for risk assessment and early detection. OBJECTIVE: We performed a systematic review and meta-analysis of the following outcomes in SDHB PV carriers: age-specific risk of developing tumors, metastatic progression, second primary tumor development, and mortality. METHODS: PubMed, MEDLINE, and EMBASE were searched. Sixteen studies met the inclusion criteria and were sorted into 4 outcome categories: age-specific penetrance, metastatic disease, risk of second tumor, and mortality. We assessed heterogeneity and performed a meta-analysis across studies using a random-effects model with the DerSimonian and Laird method. RESULTS: Penetrance of PPGLs for nonproband/nonindex SDHB PV carriers by age 20 was 4% (95% CI, 3%-6%), 11% (95% CI, 8%-15%) by age 40, 24% (95% CI, 19%-31%) by age 60%, and 35% (95% CI, 25%-47%) by age 80. The overall risk of metastatic disease for nonproband/nonindex carriers with PPGLs was 9% (95%, CI 5%-16%) per lifetime. In all affected cases (combining both proband/index and nonproband/nonindex carriers with tumors), the risk of a second tumor was 24% (95% CI, 18%-31%) and all-cause 5-year mortality was 18% (95% CI, 6%-40%). CONCLUSION: Penetrance for PPGLs in SDHB PV carriers increases linearly with age. Affected carriers are at risk of developing and dying of metastatic disease, or of developing second tumors. Lifelong surveillance is appropriate.
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