Evidence map›Paper›PMID 40336090›Full record

ArticleOrphanet journal of rare diseases2025

Leber hereditary optic neuropathy: utilities and carer burden from British and Irish participants.

Claire Lawrence, Emma Williams, Andrew Mumford, Steve Bojakowski, Julio Benedicto, Andrew Lloyd

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Trial
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Claire LawrenceAcaster Lloyd, Lacon House, 84 Theobalds Rd, London, WC1X 8NL, UK.
Emma WilliamsAcaster Lloyd, Lacon House, 84 Theobalds Rd, London, WC1X 8NL, UK.
Andrew MumfordTrustee, LHON Society, The Hayloft, Pury Hill Business Park, Alderton, Northamptonshire, NN12 7LS, UK.
Steve BojakowskiMarket Access Consultant, Bishop's Stortford, UK.
Julio BenedictoGenSight Biologics S.A., 74, Rue de Faubourg Saint-Antoine, 75012, Paris, France.
Andrew LloydAcaster Lloyd, Lacon House, 84 Theobalds Rd, London, WC1X 8NL, UK. andrew.lloyd@acasterlloyd.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeber hereditary optic neuropathy (LHON) is a rare, maternally inherited, mitochondrial disease resulting in sudden, progressive central vision loss. The condition affects numerous aspects of daily life, functioning and overall health-related quality of life (HRQL), which may spillover to carers.

methodsTwo studies were designed to estimate patient utilities associated with varying visual acuity in LHON (study 1) and to explore carer burden (study 2). In study 1, eight LHON health state vignettes (mild vision loss [LogMAR < 0.3] through to light perception [LogMAR ≥ 4]) were valued by the UK and Republic of Ireland (ROI) general pubic using the Health Utilities Index- 3 (HUI-3) and EQ-5D in an online survey (N = 360) and in time trade-off interviews (TTO; n = 120). In study 2, nine carers completed in-depth interviews exploring carer burden, the Care-related Quality of Life instrument (CarerQol), EQ-5D-5L and the Work Productivity and Activity Impairment Questionnaire (WPAI).

resultsStudy 1 demonstrated lower utilities for people with worse visual function. Mild vision loss (LogMAR < 0.3) was rated as 0.84 (HUI-3), 0.79 (EQ-5D) and 0.88 (TTO). Light perception (LogMAR ≥ 4), the most severe health state, was rated as 0.18 (HUI-3), 0.34 (EQ-5D), and 0.36 (TTO). In study 2, qualitative findings revealed substantial burden for many carers and family members. The most prominent impacts were emotional (e.g., guilt, devastation), especially related to the maternal inheritance of LHON. Impacts to carers' daily life, social life and relationships, work, and finances were also described. Standardised measures identified little impact on HRQL (EQ-5D-5L = 0.89), but some carer related burden (CarerQol-7D = 78.4). The WPAI revealed an overall work impairment of 15% and activity impairment of 37%.

conclusionsFindings suggest the HUI-3 may be more sensitive to the HRQL impact of vision loss compared to the EQ-5D and TTO method. The data indicate the potential value of an effective treatment for LHON. Qualitative findings describe the impact of LHON on carers. However, the burden described in the qualitative data was incongruent with quantitative measures, particularly the EQ-5D-5L. This demonstrates the value of conducting mixed-methods research and the importance of selecting measures which capture population-relevant concepts.

Indexed as

CaregiversOptic Atrophy, Hereditary, LeberAdolescentAdultAgedCost of IllnessFemaleHumansIrelandMaleMiddle AgedQuality of LifeSurveys and QuestionnairesUnited KingdomYoung AdultCarer burdenHealth related quality of lifeLEBER hereditary optic neuropathyLHONUtilitiesVisual acuity

Identifiers

PMID40336090
PMCPMC12060539

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.