The Resource Enzyme-replacement therapies for lysosomal storage diseases, prepared for Agency for Healthcare Research and Quality, U.S. Department of Health and Human Services ; prepared by Blue Cross and Blue Shield Association Technology Evaluation Center, Evidence-based Practice Center ; investigators, Thomas A. Ratko, Anne Marbella, Sarah Godfrey, Naomi Aronson

Enzyme-replacement therapies for lysosomal storage diseases, prepared for Agency for Healthcare Research and Quality, U.S. Department of Health and Human Services ; prepared by Blue Cross and Blue Shield Association Technology Evaluation Center, Evidence-based Practice Center ; investigators, Thomas A. Ratko, Anne Marbella, Sarah Godfrey, Naomi Aronson

Label
Enzyme-replacement therapies for lysosomal storage diseases
Title
Enzyme-replacement therapies for lysosomal storage diseases
Statement of responsibility
prepared for Agency for Healthcare Research and Quality, U.S. Department of Health and Human Services ; prepared by Blue Cross and Blue Shield Association Technology Evaluation Center, Evidence-based Practice Center ; investigators, Thomas A. Ratko, Anne Marbella, Sarah Godfrey, Naomi Aronson
Creator
Contributor
Author
Issuing body
Sponsoring body
Subject
Genre
Language
eng
Summary
BACKGROUND: Lysosomal storage diseases (LSDs) comprise about 50 unique monogenic autosomal or X-linked diseases with an estimated combined incidence of 1 in 77,000 to 88,000 live births. They occur secondary to genetic mutations that result in deficiency or reduced activity of native intracellular enzymes that catabolize biological macromolecules. These enzyme defects result in accumulation of specific macromolecular compounds within lysosomes in various tissues and organs, causing progressive damage that can become life-threatening in some diseases. LSD management traditionally involved supportive care measures tailored to disease stage, the organs and systems involved, and the degree of impairment. However, enzyme-replacement therapy (ERT) is now commercially available for six LSDs, typically used lifelong with traditional management practices for each. PURPOSE: The objective of this Technical Brief is to provide an overview of U.S. Food and Drug Administration (FDA)-approved ERT for the treatment of six LSDs. The purpose of a Technical Brief is to report what outcomes (benefits and harms) have been studied for a technology, drug or procedure; it does not enumerate those outcomes. The Technical Brief also addresses research gaps identified during its preparation. It is not intended as a comparative effectiveness review or systematic review that draws conclusions as to the clinical benefits and harms of a drug, device, or procedure. It does not assess study quality or the strength of the body of evidence on specific outcomes. METHODS: Four Guiding Questions were used to frame this Technical Brief. An inspection of the literature from 1990 through mid-April 2012 included primary studies, as well as narrative and systematic review articles to create an overview of potential clinical outcomes. Other information sources included dosing and other treatment-related information from the FDA-approved product labels; scientific information packages from the product manufacturers that included unpublished data; and, interviews with physician Key Informants and patient advocates. FINDINGS: Published clinical studies report a variety of outcomes associated with nine FDA-approved ERT products. They include disease-specific intermediate outcomes, such as plasma or urinary levels of macromolecular compounds. Others were common hematological measures (e.g., anemia, thrombocytopenia), bone pain and skeletal abnormalities, renal function, cardiac function, pulmonary function, growth, and walking tests. Harms reported to the FDA and in clinical studies were primarily allergic, including infusion-associated reactions and anaphylaxis. Immunogenic responses, primarily an IgG-type antibody response and neutralizing antibodies, have been reported. This Technical Brief identified a number of research gaps, including the need for comparative effectiveness studies, dose optimization, optimal timing for initiation of ERT, and mechanisms involved in uptake and distribution of ERT products
Member of
Cataloging source
NLM
http://library.link/vocab/creatorName
Ratko, Thomas
Funding information
Contract No. 290-2007-10058-I
Government publication
federal national government publication
Illustrations
illustrations
Index
no index present
Literary form
non fiction
Nature of contents
  • dictionaries
  • bibliography
  • technical reports
NLM call number
WD 205
http://library.link/vocab/relatedWorkOrContributorDate
1986-
http://library.link/vocab/relatedWorkOrContributorName
  • Marbella, Anne
  • Godfrey, Sarah
  • Aronson, Naomi
  • United States
  • Blue Cross and Blue Shield Association
  • Effective Health Care Program (U.S.)
Series statement
  • Technical brief
  • AHRQ publication
Series volume
  • no. 12
  • no. 12(13)-EHC154-EF
http://library.link/vocab/subjectName
  • Lysosomal Storage Diseases
  • Enzyme Replacement Therapy
Label
Enzyme-replacement therapies for lysosomal storage diseases, prepared for Agency for Healthcare Research and Quality, U.S. Department of Health and Human Services ; prepared by Blue Cross and Blue Shield Association Technology Evaluation Center, Evidence-based Practice Center ; investigators, Thomas A. Ratko, Anne Marbella, Sarah Godfrey, Naomi Aronson
Instantiates
Publication
Note
  • Title from PDF title page
  • "January 2013."
Bibliography note
Includes bibliographical references
Carrier category
online resource
Carrier category code
  • cr
Carrier MARC source
rdacarrier
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
Control code
847111336
Extent
1 online resource (various pagings)
Form of item
online
Media category
computer
Media MARC source
rdamedia
Media type code
  • c
Other physical details
illustrations.
Specific material designation
remote
System control number
(OCoLC)847111336
Label
Enzyme-replacement therapies for lysosomal storage diseases, prepared for Agency for Healthcare Research and Quality, U.S. Department of Health and Human Services ; prepared by Blue Cross and Blue Shield Association Technology Evaluation Center, Evidence-based Practice Center ; investigators, Thomas A. Ratko, Anne Marbella, Sarah Godfrey, Naomi Aronson
Publication
Note
  • Title from PDF title page
  • "January 2013."
Bibliography note
Includes bibliographical references
Carrier category
online resource
Carrier category code
  • cr
Carrier MARC source
rdacarrier
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
Control code
847111336
Extent
1 online resource (various pagings)
Form of item
online
Media category
computer
Media MARC source
rdamedia
Media type code
  • c
Other physical details
illustrations.
Specific material designation
remote
System control number
(OCoLC)847111336

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