Small hard drusen and associated factors in early seniority

PLoS One. 2022 Dec 22;17(12):e0279279. doi: 10.1371/journal.pone.0279279. eCollection 2022.

Abstract

Purpose: The purpose of this study was to examine the ocular and systemic risk profile of the fundus phenotype ≥ 20 small hard (macular) drusen (< 63 μm in diameter).

Methods: This single-center, cross-sectional study of 176 same-sex twin pairs aged 30 to 80 (median 60) years was a component of a framework study of the transition from not having age-related macular degeneration to having early AMD. Drusen categories assessed using fundus photography and optical coherence tomography included small hard drusen (diameter < 63 μm), intermediate soft drusen (63-125 μm), and large soft drusen (> 125 μm), of which the soft drusen are compatible with a diagnosis of AMD.

Results: Having ≥ 20 small hard drusen within or outside the macula was associated with increasing age, lower body mass index, shorter axial length, hyperopia, female sex, increasing high-density lipoprotein (HDL), high alcohol consumption, and with the presence of soft drusen.

Conclusions: Having ≥ 20 small hard drusen was associated with some AMD-related risk factors, but not with smoking, increasing body mass index, and higher blood pressure. Having ≥ 20 small hard drusen was also associated with soft drusen, in agreement with previous studies. These findings suggest that small hard drusen are not an early manifestation of AMD but the product of a distinct process of tissue alteration that promotes the development of AMD or some subtype thereof.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cross-Sectional Studies
  • Female
  • Humans
  • Macular Degeneration* / diagnosis
  • Retina
  • Retinal Drusen* / diagnostic imaging
  • Risk Factors
  • Tomography, Optical Coherence

Grants and funding

The study was supported by the Rigshospitalet (grant E-23334-02), P. Carl Petersens Fond (grant 19102), Helsefonden (grant 19-B-0063), Aase og Ejnar Danielsens Fond (grant 18-10-0698), Beckett Fonden (grant 19-2-3490) and Fabrikant Einar Willumsen Mindelegat (grant 500028). JB was supported by the Velux Foundations (grant 00028975). SB was supported, in part, by the OPOS Foundation. The funding organizations had no role in the design or conduct of this research.