David A. Weinstein

Prof. David A. Weinstein


Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2020 in Advances in Nutrition
Verified
Journal Article
Closed access
KRKatalin M Ross
Katalin M Ross
IFIris A Ferrecchia
Iris A Ferrecchia
KDKathryn R Dahlberg
Kathryn R Dahlberg
MDMonika Dambska
Monika Dambska
PRPatrick T Ryan
Patrick T Ryan
DWDavid A. Weinstein
David A. Weinstein
The hepatic glycogen storage diseases (GSDs) are a group of disorders where abnormal storage or release of glycogen leads to potentially life-threatening hypoglycemia and metabolic disturbances. Dietary interventions have markedly improved the outcome for these disorders, from a previously fatal condition to one where people can do well with proper care. This article chronicles the evolution of dietary management and treatment of the hepatic GSDs (types 0, I, III, VI, IX, and XI). We examine historic and current approaches for preventing hypoglycemia associated with GSDs. There is a lack of consensus on the optimal dietary management of GSDs despite decades of research, and the ongoing controversies are discussed.

1 April 2018 in Pediatric Clinics of North America
Verified
Journal Article
Closed access
DWDavid A. Weinstein
David A. Weinstein
USUlrike Steuerwald
Ulrike Steuerwald
CSCarolina F.M. De Souza
Carolina F.M. De Souza
TDTerry G.J. Derks
Terry G.J. Derks

1 June 2017 in Pediatric Diabetes
Verified
Journal Article
Closed access
PDF file
MDM Dambska
M Dambska
ELEb Labrador
Eb Labrador
CKCl Kuo
Cl Kuo
DWDavid A. Weinstein
David A. Weinstein

10 March 2025 in Journal of Inherited Metabolic Disease
Verified
Journal Article
Open access
DWDavid A. Weinstein
David A. Weinstein
TDTerry G. Derks
Terry G. Derks
DRDavid F. Rodriguez‐Buritica
David F. Rodriguez‐Buritica
AAAyesha Ahmad
Ayesha Ahmad
MCMaría‐Luz Couce
María‐Luz Couce
ECEric Crombez
Eric Crombez
Glycogen storage disease type Ia (GSDIa) is a rare, life‐threatening, inherited carbohydrate metabolism disorder caused by glucose‐6‐phosphatase (G6Pase) deficiency, which is essential for glycogenolysis and gluconeogenesis. GSDIa management includes a strict medically prescribed diet that typically includes daily uncooked cornstarch doses, including overnight, to maintain euglycemia. DTX401 is an investigational adeno‐associated virus serotype 8 vector expressing the human G6PC1 gene that encodes G6Pase. This open‐label, phase 1/2, dose‐escalation, 52‐week gene therapy trial evaluated the safety and efficacy of a single DTX401 infusion in 12 adults with GSDIa (ClinicalTrials.gov Identifier: NCT03517085). Three participants in Cohort 1 received DTX401 2.0 × 10 12 genome copies (GC)/kg, and three participants each in Cohorts 2, 3, and 4 received 6.0 × 10 12 GC/kg. Corticosteroids were administered to mitigate vector‑induced inflammatory response. All participants experienced a treatment‐emergent adverse event (TEAE) and a related TEAE. No participant experienced a dose‐limiting toxicity, TEAE leading to study discontinuation, TEAE leading to death, or serious treatment‐related TEAE. Mean (SD) time to hypoglycemia in minutes/gram of carbohydrate during a controlled fasting challenge was 5.0 (1.6) at baseline and 6.9 (2.7) at Week 52, a mean (SD) increase of 46% (72%). Mean total daily cornstarch intake was 284 g at baseline and 85 g at Week 52 in the 10 participants with available values at both time points, a mean (SD) total daily cornstarch intake reduction of 68% (20%); p < 0.001. DTX401 showed a favorable safety and efficacy profile at Week 52. Participants in all cohorts showed significant cornstarch need reductions from baseline to Week 52.

25 May 2018 in Journal of Inherited Metabolic Disease
Verified
Journal Article
Closed access
PDF file
YLYoung Mok Lee
Young Mok Lee
TCThomas J. Conlon
Thomas J. Conlon
ASAndrew Specht
Andrew Specht
KCKirsten E. Coleman
Kirsten E. Coleman
LBLaurie M. Brown
Laurie M. Brown
DWDavid A. Weinstein
David A. Weinstein

15 August 2019 in Journal of Inherited Metabolic Disease
Verified
Journal Article
Closed access
PDF file
KDKathryn R. Dahlberg
Kathryn R. Dahlberg
IFIris A. Ferrecchia
Iris A. Ferrecchia
MDMonika Dambska‐Williams
Monika Dambska‐Williams
TRTraci E. Resler
Traci E. Resler
KRKatalin M. Ross
Katalin M. Ross
DWDavid A. Weinstein
David A. Weinstein