Evidence map›Paper›PMID 28569047›Full record

Trial reportAmerican journal of hematology2017

Transformation in pretreatment manifestations of Gaucher disease type 1 during two decades of alglucerase/imiglucerase enzyme replacement therapy in the International Collaborative Gaucher Group (ICGG) Gaucher Registry.

Pramod K Mistry, Julie L Batista, Hans C Andersson, Manisha Balwani, Thomas Andrew Burrow, Joel Charrow, Paige Kaplan, Aneal Khan, Priya S Kishnani, Edwin H Kolodny and 3 more

Registry-linked trialOpen access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in American journal of hematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00358943 (Gaucher Disease Registry Protocol), which is not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-weighted citation impact, top 10% 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.

NCT00358943 recruitingnot on this map

Gaucher Disease Registry Protocol

Typeobservational_patient_registrySponsorGenzyme, a Sanofi CompanyRan1991 to 2034Enrolled12,000ConditionsGaucher Disease, Cerebroside Lipidosis Syndrome, Glucocerebrosidase Deficiency Disease, Glucosylceramide Beta-Glucosidase Deficiency Disease
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 56 citations in OpenAlex.

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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

13 authors at 13 institutions in 2 countries.

Pramod K MistryDepartment of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut.ORCID http://orcid.org/0000-0003-3447-6421
Julie L BatistaSanofi Genzyme, Cambridge, Massachusetts.
Hans C AnderssonHayward Genetics Center, Tulane University Medical School, New Orleans, Louisiana.
Manisha BalwaniIcahn School of Medicine at Mount Sinai, New York City, New York.
Thomas Andrew BurrowCollege of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Joel CharrowNorthwestern University Feinberg School of Medicine, Chicago, Illinois.
Paige KaplanChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Aneal KhanThe University of Calgary, Calgary, Alberta, Canada.
Priya S KishnaniDivision of Medical Genetics, Duke University School of Medicine, Durham, North Carolina.
Edwin H KolodnyNew York University School of Medicine, New York, New York.
Barry RosenbloomCedars-Sinai/Tower Hematology Oncology, Beverly Hills, California.
C Ronald ScottUniversity of Washington, Seattle, Washington.
Neal WeinrebDepartments of Human Genetics and Medicine (Hematology), University of Miami Miller School of Medicine, Miami, Florida.ORCID http://orcid.org/0000-0001-9100-4733
Cedars-Sinai Medical Center · USChildren's Hospital of Philadelphia · USDuke University · USIcahn School of Medicine at Mount Sinai · USNew York University · USNorthwestern University · USSanofi (United States) · USTulane University · USUniversity of Arkansas for Medical Sciences · USUniversity of Calgary · CAUniversity of Miami · USUniversity of Washington · USYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Understanding the skeletal phenotype of Gaucher diseaseR01AR065932 · NIAMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MISTRY, PRAMOD K, ZAIDI, MONE · 2013 to 2017
$2.6M
NCATS NIH HHS UL1 TR001863NIAMS NIH HHS R01 AR065932
6 · The paper itself

Abstract

This study tests the hypothesis that the prevalence of severe clinical manifestations in Gaucher disease type 1 (GD1) patients at the time of treatment initiation has changed since alglucerase/imiglucerase enzyme replacement therapy (ERT) was approved in the United States (US) in 1991. US alglucerase/imiglucerase-treated GD1 patients from the International Collaborative Gaucher Group Gaucher Registry clinicaltrials.gov NCT00358943 were stratified by age at ERT initiation (<18, 18 to <50, ≥50 years), era of ERT initiation (1991-1995, 1996-2000, 2001-2005, 2006-2009), and splenectomy status pre-ERT. Prevalence of splenectomy decreased dramatically across the eras among all age groups. Bone manifestations were more prevalent in splenectomized patients than non-splenectomized patients in all age groups. Prevalence of bone manifestations differed across eras in certain age groups: non-splenectomized patients had a lower prevalence of ischemic bone events (pediatric patients) and bone crisis (pediatric patients and adults 18 to <50 years) in later eras; splenectomized adult (18 to <50 years) patients had a lower prevalence of ischemic bone events and bone crisis in later eras. Over two decades after the introduction of ERT, the prevalence of splenectomy and associated skeletal complications has declined dramatically. Concomitantly, the interval between diagnosis and initiation of ERT has decreased, most strikingly in pediatric patients who have the most severe disease. Together, these findings suggest that since the introduction of alglucerase/imiglucerase ERT, optimal standard of care has become established in the US to prevent destructive complications of GD1.

Indexed as

Enzyme Replacement TherapyAdolescentAdultFemaleFollow-Up StudiesGaucher DiseaseGlucosylceramidaseHumansMaleMiddle AgedPrevalenceRegistriesSplenectomyalgluceraseGlucosylceramidaseimiglucerase

Identifiers

PMID28569047
PMCPMC5600096
OpenAlexW2617335676

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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.