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Survival is affected by mutation type and molecular mechanism in vascular Ehlers–Danlos syndrome (EDS type IV)
Open accessAbstract
Purpose We sought to characterize the natural history of vascular Ehlers-Danlos syndrome in individuals with heterozygous COL3A1 mutations.Methods We reviewed clinical records for details of vascular, bowel, and organ complications in 1,231 individuals (630 index cases and 601 relatives).Results Missense and splice-site mutations accounted for more than 90% of the 572 alterations that we had identified in COL3A1. Median survival was 51 years but was influenced by gender (lower in men) and by the type of mutation.Conclusion Although vascular Ehlers-Danlos syndrome appears to be genetically homogeneous, allelic heterogeneity is marked, and the natural history varies with gender and type of mutation in COL3A1. These findings indicate that when counseling families, confirmation of the presence of a COL3A1 mutation and its nature can help evaluate the risks of complications. These data are also important ingredients in both the selection and allocation of individuals to appropriate arms in clinical trials to assess the effects of interventions.
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In the citing paper
“The majority of disease-causing variants in COL3A1 are glycine substitutions and in-frame splice mutations in the triple helix domain”
In the citing paper
“through a dominant negative effect are associated with the severe clinical spectrum potentially lethal of vEDS, characterized by fragility of soft connective tissues with arterial and organ ruptures.”
In the citing paper
“This type of mutations produces a dominant negative effect on the protein, thereby inhibiting extracellular accumulation of mature COLLIII.”
In the citing paper
“Substitutions of bulky residues (Arg, Asp, Glu, Val) for glycine residues in the triple helical domain are usually less severe than splice site mutations, but more consequential than substitutions by smaller residues (Ala, Ser, Cys).”
In the citing paper
“the nature of the specific COL3A1 mutation influences life expectancy.”
In the citing paper
“Splice site mutations that lead to exon skipping have the lowest median survival.”
In the citing paper
“Heterozygosity for COL3A1 null alleles typically produces a milder clinical phenotype with a significant delayed onset of complications [4, 9–12].”
In the citing paper
“COL3A1 missense mutations altering the glycine codons together with in-frame splice mutations in the triple helical domain account for the majority of disease-causing variants and lead to misfolding of COLLIII in the endoplasmic reticulum (ER) and retention of seven eighths of misfolded procollagen trimers in the cell with consequent enlargement of ER vesicles [8–10].”
In the citing paper
“Besides, the present patients exhibited a full-blown expression of the disease with several major arterial events, in line with the limited genotype-phenotype correlation that associates this type of structural mutations with a more severe clinical phenotype [4,9–12].”
Citations
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Self-citationPregnancy-related deaths and complications in women with vascular Ehlers–Danlos syndrome
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Items 301–313 of 313
Liu, Z., Fang, X., Wang, A., Xu, P., Yin, Y., Li, R., Huang, C., Duan, L., & Qi, H. (2026) · European Journal of Medical Genetics · doi:10.1016/j.ejmg.2026.105102
Лучевая диагностика аневризмы верхней брыжеечной артерии. Клинический случай
Сергеевна, П. В., Bl, S., Анатольевич, Д. А., Дубицкий, Д. Л., & Игнашев, К. В. (2026) · Vizualizaciâ v medicine. · doi:10.56871/vim.2026.53.96.004
Prakash, S. K., & Angueira, A. R. (2026) · Springer eBooks · doi:10.1007/978-3-032-35473-0_12
Genetics of Heritable Thoracic Aortic Diseases
Freire, J. L., & Boileau, C. (2026) · Springer eBooks · doi:10.1007/978-3-032-35473-0_9
Aortopathy in Loeys-Dietz Syndrome and Vascular Ehlers-Danlos Syndrome
Backer, J. F. A. D., Teixidó‐Turà, G., & Evangelista, A. (2026) · Springer eBooks · doi:10.1007/978-3-032-35473-0_11
Genetic Aortic Disease in the Pediatric Population
Mosquera, L. M., Cervi, E., & Sabaté-Rotés, A. (2026) · Springer eBooks · doi:10.1007/978-3-032-35473-0_13
Horiguchi, N., Hisanaga, E., Sato, H., Yoshida, K., Kimura, A., Ito, A., HORITA, M., Suzuki, A., & Kawai‐Kowase, K. (2026) · Journal of General and Family Medicine · doi:10.1002/jgf2.70183
若年者の非外傷性両下腿コンパートメント症候群を契機に診断された血管型エーラス・ダンロス症候群の1例
篠原, 大., 善家, 雄., 太田, 克., 佐藤, 直., 岡田, 祥., & 酒井, 昭. (2026) · Orthopedics & Traumatology · doi:10.5035/nishiseisai.75.867
Vascular Ehlers–Danlos Syndrome (vEDS)
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Corrao, S., Ruggeri, M. I., Benedetto, A. D., Corrao, G., Calvo, L., & Scibetta, S. (2026) · Journal of Internal Medicine · doi:10.1111/joim.70165
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Long, B., Tannenbaum, L., & Sandefur, B. J. (2026) · Journal of Emergency Medicine · doi:10.1016/j.jemermed.2026.09.018
闰珂珂, Yuan, Y., Wen, X., Hu, X., & Zhu, D. (2026) · Frontiers in Pediatrics · doi:10.3389/fped.2026.1883212
Metadata
- Authors
- Pepin, M. G., Schwarze, U., Rice, K. M., Liu, M., Leistritz, & Byers, P. H.
- Affiliations
- University of Washington (US)
- Corresponding author
- Pepin, Melanie G.
- Venue
- Genetics in Medicine
- Publisher
- Elsevier BV
- Published
- 2014-12
- Volume
- 16
- Issue
- 12
- Pages
- 881-888
- ISSN
- 1098-3600 (ISSN-L)
- OpenAlex
- W2030732677
- Cited by
- 313
- References
- 16
- Citations by year
- 2026: 29 · 2025: 30 · 2024: 35 · 2023: 29 · 2022: 37 · 2021: 27 · 2020: 24 · 2019: 30 · 2018: 26 · 2017: 18 · 2016: 16 · 2015: 10 · 2014: 2
- FWCI
- 10.04
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Genetics in Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Connective tissue disorders research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Dermatological and Skeletal Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Keywords
- vascular Ehlers-Danlos syndrome, COL3A1 mutation, missense mutations, splice site mutation, natural history (disease), survival, allelic heterogeneity, gender differences, bowel complications, vascular complications, family counseling, clinical trial selection
- MeSH terms
- Adolescent, Adult, Aged, Aged, 80 and over, Alleles, Child, DNA Mutational Analysis, Ehlers-Danlos Syndrome, Female, Humans, Male, Middle Aged, Mutation, RNA Splicing, Genetic Variation, Treatment Outcome, Mutation, Missense, Collagen Type III, Young Adult
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