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ArticleIndian journal of pediatrics2026

Impact of Enzyme Replacement Therapy on Patients with Late Onset Pompe Disease - Real World Data from a Developing Country.

Swasti Pal, Sunita Bijarnia-Mahay, Sheela Nampoothiri, Mamta Muranjan, Neerja Gupta, Sankar Vh, Sujatha Jagadeesh, Meenakshi Bhat, Sanjeeva Gn, Dhanya Yesodharan and 4 more

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Article in Indian journal of pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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5 · Who and what money

Authors and funding

14 authors.

Swasti PalInstitute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India.
Sunita Bijarnia-MahayInstitute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India.
Sheela NampoothiriDepartment of Pediatric Genetics, Amrita Institute of Medical Sciences, Kochi, Kerala, India.
Mamta MuranjanDepartment of Pediatrics, King Edward Memorial Hospital, Mumbai, India.
Neerja GuptaDivision of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Sankar VhDepartment of Medical Genetics, Sree Avittom Thirunal (SAT) Hospital, Government Medical College, Thiruvananthapuram, Kerala, India.
Sujatha JagadeeshDepartment of Clinical Genetics & Genetic Counselling, Mediscan Systems, Chennai, India.
Meenakshi BhatDepartment of Clinical Genetics, Centre for Human Genetics, Bengaluru, India.
Sanjeeva GnDepartment of Pediatrics, Indira Gandhi Institute of Child Health, Bengaluru, India.
Dhanya YesodharanDepartment of Pediatric Genetics, Amrita Institute of Medical Sciences, Kochi, Kerala, India.
Prerana ModaniDivision of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Madhulika KabraIndian Council of Medical Research, All India Institute of Medical Sciences, New Delhi, India.
Priya S KishnaniDivision of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, USA.
Ratna Dua PuriInstitute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India. ratnadpuri@yahoo.com.ORCID http://orcid.org/0000-0003-2694-6147

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo determine the impact of enzyme replacement therapy (ERT) in patients with late onset Pompe disease (LOPD) in terms of change in motor and respiratory status, along with challenges in obtaining multi-disciplinary care to manage the multi-systemic aspects of disease.

methodsThis was a retrospective chart review of patient data, collected from seven tertiary care centres across India. All patients of late onset Pompe disease that have received enzyme replacement therapy were included and a descriptive analysis of data was performed.

resultsTwenty two patients of LOPD were initiated on ERT and included in this data analysis, with demise of three patients and incomplete follow-up of five patients. Motor function assessment, in terms of 6 min walk test (6MW) and change in ambulatory status, showed improvement/stabilization of distance walked in 6 min for three of four patients, although one of three lost ambulation thereafter due to severe COVID infection. One patient showed gradual deterioration in 6 MW distance with 6.7% minimal detectable change for 4 patients. Fifteen percent (15%) patients lost independent ambulation over the study period. Of eight patients with pulmonary function test data before and after ERT, four showed decline while four showed stabilization of supine and sitting forced vital capacity. Three patients developed sleep disordered breathing requiring nocturnal BiPAP. Five patients were switched over to avalglucosidase alfa from alglucosidase alfa, with two patients showing improvement in PFT after switching over.

conclusionsThis is the first study describing the impact of ERT in an Indian cohort of LOPD patients. It shows real world concerns of impact of chronic diseases with delay in starting therapy. It also brings to light the challenges in obtaining multi-disciplinary management. The wide variability in spectrum of presentations, early onset and faster rates of disease progression as well as high disease burden highlight the need for early initiation of therapy.

Indexed as

Enzyme Replacement TherapyGlycogen Storage Disease Type IIAdolescentalpha-GlucosidasesChildDeveloping CountriesFemaleHumansIndiaMaleRetrospective StudiesTreatment Outcomealpha-GlucosidasesAlglucosidase alfaAvalglucosidase alfaChronic neuromuscular disorderERTLimb-girdle muscular dystrophyLOPD

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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.