Media release
From:
British Journal of Ophthalmology
Cholesterol and diabetes drugs may lessen risk of degenerative eye disease of ageing
Use linked to lower prevalence of age related macular degeneration in European populations
Regular use of drugs to lower cholesterol and control type 2 diabetes may lessen the risk of the degenerative eye disease associated with ageing, known as AMD, finds a pooled data analysis of the available evidence, published online in the British Journal of Ophthalmology.
These common drugs are linked to lower prevalence of AMD (age related macular degeneration) in European populations, the results show.
AMD is the leading cause of severe visual impairment among older people in high-income countries. In Europe alone, 67 million people currently have the condition, with new cases projected to soar over the next few decades as populations age.
AMD affects central vision and the ability to see fine detail. Various genetic and environmental factors associated with ageing are thought to trigger AMD, but it’s still not clear how best to prevent it or slow its progression.
Previously published research suggests that drugs to lower cholesterol, control diabetes, and dampen down inflammation may help to lessen the risk of developing AMD, but these findings were partly contradictory and based on small numbers of participants.
In a bid to get round these issues, the researchers pooled the results of 14 population-based and hospital-based studies, involving 38,694 people from France, Germany, Greece, Ireland, Italy, Norway, Portugal, Russia and the UK.
The studies were part of the European Eye Epidemiology (E3) consortium, a collaborative pan European network, the principal aim of which is to develop and analyse large pooled datasets to further the understanding of eye disease and sight loss.
Participants were all over the age of 50 and taking at least one of the following types of drug to: lower cholesterol, including statins; control diabetes, including insulin; to dampen down inflammation, excluding steroids; and Levodopa, used to treat movement disorders caused by neurodegenerative disease.
The prevalence of AMD ranged from 12% to 64.5% across the included studies—9332 cases in total—while the prevalence of advanced (late) AMD ranged from 0.5% to 35.5%—951 cases in total.
The pooled data analysis showed that drugs to lower cholesterol or control diabetes were associated with, respectively, 15% and 22% lower prevalence of any type of AMD, after accounting for potentially influential factors.
No such associations were found for any of the other types of drug or for advanced AMD, in particular, although there were only a relatively small number of such cases, note the researchers.
Theirs is the first large pooled data analysis of its kind to use individual level data from various population-based and hospital-based studies, highlight the researchers.
“Yet, further longitudinal data are needed to confirm our findings, which are inherently limited by using cross-sectional data only and cannot infer causality,” they caution.
But the findings point to a likely key role for metabolic processes in the development of AMD, which may offer potential new avenues for treatment and have implications for public health messaging, they suggest.
“Our study suggests that regular intake of [lipid lowering] and antidiabetic drugs is associated with reduced prevalence of AMD in the general population. Given a potential interference of these drugs with pathophysiological pathways relevant in AMD, this may contribute to a better understanding of AMD aetiology,” they conclude.
Journal/
conference:
British Journal of Ophthalmology
Organisation/s:
The University of Sydney, University Hospital Bonn, Germany
Funder:
The Alienor study received financial support from Laboratoires Théa
(Clermont-Ferrand,
France). Laboratoires Théa participated in the design of the
study, but no sponsor participated in the collection, management, statistical analysis
and interpretation of the data, nor in the preparation, review or approval of the
present manuscript. The Gutenberg Health Study is funded through the government
of Rhineland-Palatinate
(’Stiftung Rheinland-Pfalz
fuer Innovation’, contract AZ
961-386261/
733), the research programmes ’Wissen schafft Zukunft’ and ’Center
for Translational Vascular Biology (CTVB)’ of the Johannes Gutenberg University of
Mainz, and its contract with Boehringer Ingelheim and PHILIPS Medical Systems,
including an unrestricted grant for the Gutenberg Health Study. AKS holds the
professorship for ophthalmic healthcare research endowed by ’Stiftung Auge’ and
financed by ’Deutsche Ophthalmologische Gesellschaft’ and ’Berufsverband der
Augenärzte Deutschland e.V.’. AugUR: Investigations and analyses are supported
by grants from the German Federal Ministry of Education and Research (BMBF
01ER1206, BMBF 01ER1507 to IMH), by the Deutsche Forschungsgemeinschaft
(DFG, German Research Foundation; HE 3690/7-1
and HE 3690/5-1
to IMH, BR
6028/2-1
to CB) and by the National Institutes of Health (NIH R01 EY RES 511967
to IMH). MARS (Münster Aging and Retina Study) was supported by Deutsche
Forschungsgemeinschaft (DFG) Grants HE 2293/5-1,
5-2,
5-3
and PA 357/7-1,
the
Intramural International Monetary Fund of the University of Muenster, the Pro Retina
Foundation and the Jackstaedt Foundation (DP, HWH). The EPIC-Norfolk
study (DOI
10.22025/2019.10.105.00004) has received funding from the Medical Research
Council (MR/N003284/1 and MC-UU_
12015/1) and Cancer Research UK (C864/
A14136). The clinic for the third health examination was funded by Research into
Ageing (262). We are grateful to all the participants who have been part of the
project and to the many members of the study teams at the University of Cambridge
who have enabled this research. AK is funded by a UKRI Future Leaders Fellowship
(Medical Research Council MR/T040912/1). RNL is funded by a Moorfields Eye
Charity Springboard Award. PJF is supported by an unrestricted grant from Alcon
and the Desmond Foundation. This publication is supported by the Leipzig Research
Centre for Civilization Diseases (LIFE), an organisational unit affiliated to the Medical
Faculty of Leipzig University. LIFE is funded by means of the European Union, by
the European Regional Development Fund (ERDF) and by funds of the Free State of Saxony within the framework of the excellence initiative (project numbers: 713-241202,
14505/2470, 14575/2470). FGR is supported by a grant from the German
Federal Ministry of Education and Research: i:DSem—Integrative data semantics in
systems medicine (031L0026). The authors wish to express their sincere thanks to
the participants of LIFE-Adult
for their time. The authors gratefully acknowledge KW
and her team at the Leipzig Research Center for Civilization Diseases (LIFE-Adult),
Leipzig University, Leipzig, Germany for data acquisition. The NICOLA study is
funded by the Atlantic Philanthropies, the Economic and Social Research Council,
the UKCRC Centre of Excellence for Public Health Northern Ireland, the Centre for
Aging Research and Development in Ireland, the Office of the First Minister and
Deputy First Minister, the Health and Social Care Research and Development Division
of the Public Health Agency, the Wellcome Trust/Wolfson Foundation and Queen’s
University Belfast. CRESCENDO study was carried out with the financial support of
the ANR—Agence Nationale de la Recherche (MALZ-007-
01—
The French National
Research Agency—and grants from the “Chercheur d’Avenir” (R12028FF) and Aide
à la Recherche en Partenariat avec les Entreprises (ARPE; RPH12007F) allocated by
the Languedoc Roussillon administrative regional district (France). The Coimbra Eye
Study was funded by Novartis.