Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
Long-term blood pressure variability and risk of age-related macular degeneration in older adults: the ALIENOR study.
Author Affiliations & Notes
  • Blondy KAYEMBE MULUMBA
    INSERM U1219 - BPH, Universite de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France
  • Karen LEFFONDRE
    INSERM U1219 - BPH, Universite de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France
  • Benedicte Mj Merle
    INSERM U1219 - BPH, Universite de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France
  • Jean-Francois Korobelnik
    INSERM U1219 - BPH, Universite de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France
    Service d'Ophtalmologie, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France
  • Catherine HELMER
    INSERM U1219 - BPH, Universite de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France
  • Cecile Delcourt
    INSERM U1219 - BPH, Universite de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France
  • Audrey Cougnard-Gregoire
    INSERM U1219 - BPH, Universite de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France
  • Marie-Noëlle DELYFER
    INSERM U1219 - BPH, Universite de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France
    Service d'Ophtalmologie, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France
  • Footnotes
    Commercial Relationships   Blondy KAYEMBE MULUMBA None; Karen LEFFONDRE None; Benedicte Merle Laboratoires Théa, Code F (Financial Support); Jean-Francois Korobelnik Abbvie, Apellis, Bayer, Eyepoint Pharma, Janssen, NanoRetina, Opthea, Roche, Thea, Carl Zeiss Meditec, Code C (Consultant/Contractor), Alexion, Novonordisk, Oxular, Code S (non-remunerative); Catherine HELMER None; Cecile Delcourt Allergan, Apellis, Chauvin-Bausch+Lomb, Laboratoires Théa, Novartis, Code C (Consultant/Contractor); Audrey Cougnard-Gregoire None; Marie-Noëlle DELYFER Abbvie, Bayer, Horus Pharma, Novartis, Roche, Code C (Consultant/Contractor)
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 1342. doi:
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      Blondy KAYEMBE MULUMBA, Karen LEFFONDRE, Benedicte Mj Merle, Jean-Francois Korobelnik, Catherine HELMER, Cecile Delcourt, Audrey Cougnard-Gregoire, Marie-Noëlle DELYFER; Long-term blood pressure variability and risk of age-related macular degeneration in older adults: the ALIENOR study.. Invest. Ophthalmol. Vis. Sci. 2024;65(7):1342.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Long-term blood pressure variability (BPV) has emerged as a risk factor for various health problems, including eye diseases. Yet, its role on age-related macular degeneration (AMD) onset remains unknown. This population-based longitudinal cohort study aimed to test the hypothesis that a higher BPV is associated with an increased risk of early or advanced AMD in older adults.

Methods : The ALIENOR (Antioxidants, LIpides Essentiels, Nutrition et maladies OculaiRes) study included 963 participants aged 73 years and older from the 3-City study (3C), followed every 2-3 years in Bordeaux, France (2006-2020). We analyzed those who had at least two blood pressure (BP) measurements, and were free of early and/or advanced AMD at baseline, according to the form studied. BP was measured every 2-3 years in 3C (1999-2017). Systolic (SBPV), diastolic (DBPV) and pulse (PPV) BPV were determined by the standard deviation method at each visit and considered as time-dependent variables. AMD was classified using retinal color photographs and optical coherence tomography imaging. After multiple imputation on covariates, shared random effects joint models fitted individual BPV trajectories (longitudinal data) and quantified their effect on AMD onset (survival data). Using the R package JMbayes2, the Bayesian approach yielded mean adjusted Hazard Ratios (aHR) of AMD and their 95% credible intervals (95%CrI).

Results : Of 475 and 692 participants analyzed, 36% and 10% developed respectively early and advanced AMD, after a mean follow-up of 8 years. BPV was not associated with an increased risk of early AMD (aHR: 0.95, 95%CrI: 0.81–1.09, p=0.47; aHR: 0.95, 95%CrI: 0.71–1.30, p=0.75; and aHR: 0.90, 95%CrI: 0.75–1.06, p=0.21; for a 5-mmHg increase in SBPV, DBPV and PPV respectively). Conversely, the risk of advanced AMD was significantly 60% higher for a 5-mmHg increase in DBPV (aHR: 1.60, 95%CrI: 1.05–2.43, p=0.03), whereas significance was not reached for a 5-mmHg increase in SBPV (aHR: 1.20, 95%CrI: 0.95–1.52, p=0.12) and PPV (aHR: 1.13, 95%CrI: 0.85–1.49, p=0.39). Complete case analysis revealed similar results.

Conclusions : Among BPV components, only higher DBPV was associated with an increased risk of advanced AMD, and none was associated with an increased risk of early AMD. However, replicating the study in other contexts is necessary to confirm these results.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

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