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1000 Titel
  • Prevalence and determinants of subretinal drusenoid deposits in patients’ first-degree relatives
1000 Autor/in
  1. Mauschitz, Matthias M. |
  2. Hochbein, Benedikt J. |
  3. Klinkhammer, Hannah |
  4. Saßmannshausen, Marlene |
  5. Terheyden, Jan H. |
  6. Krawitz, Peter |
  7. Finger, Robert P. |
1000 Verlag Springer Berlin Heidelberg
1000 Erscheinungsjahr 2023
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2023-09-06
1000 Erschienen in
1000 Quellenangabe
  • 262(1):53-60
1000 Copyrightjahr
  • 2023
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00417-023-06221-y |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10805990/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Purpose</jats:title> <jats:p>Subretinal drusenoid deposits (SDDs) are distinct extracellular alteration anterior to the retinal pigment epithelium (RPE). Given their commonly uniform phenotype, a hereditary predisposition seems likely. Hence, we aim to investigate prevalence and determinants in patients’ first-degree relatives.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>We recruited SDD outpatients at their visits to our clinic and invited their relatives. We performed a full ophthalmic examination including spectral domain–optical coherence tomography (SD-OCT) and graded presence, disease stage of SDD as well as percentage of infrared (IR) en face area affected by SDD. Moreover, we performed genetic sequencing and calculated a polygenic risk score (PRS) for AMD. We conducted multivariable regression models to assess potential determinants of SDD and associations of SDD with PRS.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>We included 195 participants, 123 patients (mean age 81.4 ± 7.2 years) and 72 relatives (mean age 52.2 ± 14.2 years), of which 7 presented SDD, resulting in a prevalence of 9.7%. We found older age to be associated with SDD presence and area in the total cohort and a borderline association of higher body mass index (BMI) with SDD presence in the relatives. Individuals with SDD tended to have a higher PRS, which, however, was not statistically significant in the multivariable regression.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusion</jats:title> <jats:p>Our study indicates a potential hereditary aspect of SDD and confirms the strong association with age. Based on our results, relatives of SDD patients ought to be closely monitored for retinal alterations, particularly at an older age. Further longitudinal studies with larger sample size and older relatives are needed to confirm or refute our findings.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Genetic Risk Score [MeSH]
lokal Aged, 80 and over [MeSH]
lokal Aged [MeSH]
lokal Adult [MeSH]
lokal Retinal Drusen/epidemiology [MeSH]
lokal Age-related macular degeneration
lokal Humans [MeSH]
lokal Middle Aged [MeSH]
lokal Retinal Drusen/diagnosis [MeSH]
lokal Imaging
lokal Retinal Disorders
lokal Fluorescein Angiography [MeSH]
lokal Retinal Drusen/genetics [MeSH]
lokal Genetics
lokal Subretinal drusenoid deposits
lokal Retinal Pigment Epithelium [MeSH]
lokal Tomography, Optical Coherence/methods [MeSH]
lokal Prevalence [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/TWF1c2NoaXR6LCBNYXR0aGlhcyBNLg==|https://frl.publisso.de/adhoc/uri/SG9jaGJlaW4sIEJlbmVkaWt0IEou|https://frl.publisso.de/adhoc/uri/S2xpbmtoYW1tZXIsIEhhbm5haA==|https://frl.publisso.de/adhoc/uri/U2HDn21hbm5zaGF1c2VuLCBNYXJsZW5l|https://frl.publisso.de/adhoc/uri/VGVyaGV5ZGVuLCBKYW4gSC4=|https://frl.publisso.de/adhoc/uri/S3Jhd2l0eiwgUGV0ZXI=|https://frl.publisso.de/adhoc/uri/RmluZ2VyLCBSb2JlcnQgUC4=
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  1. Rheinische Friedrich-Wilhelms-Universität Bonn |
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    1000 Förderer Rheinische Friedrich-Wilhelms-Universität Bonn |
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