Evidence map›Paper›PMID 26937390›Full record

ArticleMolecular genetics and metabolism reports2015

Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysis.

Michael Beck, Derralynn Hughes, Christoph Kampmann, Sylvain Larroque, Atul Mehta, Guillem Pintos-Morell, Uma Ramaswami, Michael West, Anna Wijatyk, Roberto Giugliani and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics and metabolism reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 2 pooled it
9.2field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

61 citing papers in PubMed, 2 syntheses or guidelines pooled it, 128 citations in OpenAlex.

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  18. Treatment of Fabry Nephropathy: A Literature Review.Medicina (Kaunas, Lithuania) · 2023
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1 more citing papers are in PubMed but not listed here.

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

11 authors at 6 institutions in 6 countries.

Michael BeckUniversity Medical Center, University of Mainz, Department of Paediatrics, Mainz, Germany.
Derralynn HughesRoyal Free London NHS Foundation Trust, University College of London, UK.
Christoph KampmannUniversity Medical Center, University of Mainz, Department of Paediatrics, Mainz, Germany.
Sylvain LarroqueShire, Zug, Switzerland.
Atul MehtaRoyal Free London NHS Foundation Trust, University College of London, UK.
Guillem Pintos-MorellDepartment of Pediatrics, University Hospital "Germans Trias i Pujol," Badalona, Universitat Autònoma de Barcelona, Spain.
Uma RamaswamiRoyal Free London NHS Foundation Trust, University College of London, UK.
Michael WestDepartment of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.
Anna WijatykShire, Lexington, MA, USA.
Roberto GiuglianiMedical Genetics Service HCPA/Dep Genet UFRGS and INAGEMP, Porto Alegre, Brazil.
Fabry Outcome Survey Study Group
Royal Free London NHS Foundation Trust · GBJohannes Gutenberg University Mainz · DEDalhousie University · CATakeda (United States) · USUniversidade Federal do Rio Grande do Sul · BRUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Outcomes from 5 years of treatment with agalsidase alfa enzyme replacement therapy (ERT) for Fabry disease in patients enrolled in the Fabry Outcome Survey (FOS) were compared with published findings for untreated patients with Fabry disease. Data were extracted from FOS, a Shire-sponsored database, for comparison with data from three published studies. Outcomes evaluated were the annualized rate of change in estimated glomerular filtration rate (eGFR) and left ventricular mass indexed to height (LVMI) as well as time to and ages at a composite morbidity endpoint and at death. FOS data were extracted for 740 treated patients who were followed for a median of ~ 5 years. Compared with no treatment, patients treated with agalsidase alfa demonstrated slower decline in renal function and slower progression of left ventricular hypertrophy. Treated male patients with baseline eGFR < 60 mL/min/1.73 m(2) had a mean (standard error of the mean [SEM]) annualized change in eGFR of - 2.86 (0.53) mL/min/1.73 m(2)/y compared with - 6.8 (1.5) in the published untreated cohort. The mean (SEM) rate of LVMI increase with treatment was 0.33 (0.10) g/m(2.7)/y in males and 0.48 (0.09) in females, compared with 4.07 (1.03) in untreated males and 2.31 (0.81) in untreated females. Morbidity occurred later in treated patients, with ~ 16% risk of a composite morbidity event (26% in males) after 24 months with ERT versus ~ 45% without treatment, with first events and deaths also occurring at older ages in patients administered ERT (e.g., estimated median survival in treated males was 77.5 years versus 60 years in untreated males). Findings from these retrospective comparisons of observational data and published literature support the long-term benefits of ERT with agalsidase alfa for Fabry disease in slowing the progression of renal impairment and cardiomyopathy. Treatment also appeared to delay the onset of morbidity and mortality. Interpretation of these findings should take into account that they are based on retrospective comparisons with previously published data.

Indexed as

ACEI, Angiotensin-converting enzyme inhibitorAgalsidase alfaARB, Angiotensin receptor blockerCI, Confidence intervaleGFR, Estimated glomerular filtration rateEnzyme replacement therapyERT, Enzyme replacement therapyFabry diseaseFOS, Fabry Outcome SurveyLong-term effectivenessLVH, Left ventricular hypertrophyLVMI, Left ventricular mass indexed to heightMDRD, Modification of Diet in Renal DiseaseSEM, Standard error of the meanSE, Standard error

Identifiers

PMID26937390
PMCPMC4750577
OpenAlexW1989708725

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.