Clinical characteristics and prognosis of SDHD pathogenic variant carriers: a systematic review and meta-analysis

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Authors: Xinquan Lian, Liping Shen, Jiayin Song, Mengqi Pang, Yunmeng Zhong, Haitao Zhang, Yadong Xing, Tao-Hsin Tung, Bo Shen
Cited by: 1
References: 30

Abstract

Background Germline pathogenic variants (PVs) of succinate dehydrogenase subunit D ( SDHD ) are major genetic causes of pheochromocytomas and paragangliomas. Existing studies have reported inconsistent findings and lack a comprehensive synthesis regarding penetrance, multifocality and metastatic risk in carriers of SDHD PVs. Objective To systematically assess age-specific penetrance (in all carriers) and the proportions of multifocality, metastatic disease and mortality among affected carriers, and explore potential genotype–phenotype associations through a systematic review and meta-analysis. Methods Eligible observational studies were selected from PubMed, MEDLINE and EMBASE that reported age-specific penetrance (in all carriers) and the proportions of multifocality, metastatic disease and mortality among affected carriers (those with tumours). Additionally, data on specific SDHD variants associated with tumour multifocality or metastatic behaviour were collected. Following independent data extraction and quality assessment by two reviewers, these proportions were meta-analysed using random-effects models or fixed-effect model to generate pooled estimates with 95% CIs and prediction intervals. Results Age-specific penetrance increased from 20% at 20 years of age (95% CI 16% to 25%) to 58% at 40 years (95% CI 48% to 67%) and 82% at 60 years (95% CI 75% to 90%). Among the affected SDHD PV carriers, the pooled proportions were 75% (95% CI 72% to 79%) for multifocal tumours, 3% (95% CI 2% to 4%) for metastatic disease and 1% (95% CI 1% to 2%) for mortality. Conclusion SDHD PV carriers exhibit increasing age-specific penetrance, with a high proportion of patients having multifocal tumours but low proportions of metastatic disease and mortality, providing partial evidence for the need for lifelong monitoring of SDHD PV carriers. However, evidence linking specific variants to these phenotypes is limited and requires further investigation. PROSPERO registration number CRD420251060752.

Fields of Study & Subjects

Adrenal and Paraganglionic Tumors Neuroblastoma Research and Treatments Hormonal Regulation and Hypertension

Publication details

Journal / source
Journal of Medical Genetics
Publisher
BMJ
Volume
63
Issue
8
Pages
467–473
Publication date
15 April 2026
Language
EN