# Oral Cornstarch and Glycyrrhizin Improve Severe Liver Injury Caused by Glycogen Storage Disease Type IXa

**Authors:** Masanori Miyaishi, Kenji Fukushima, Naomi Kuranobu, Jun Murakami, Noriyuki Namba

PMC · DOI: 10.7759/cureus.78396 · Cureus · 2025-02-02

## TL;DR

A young boy with liver injury from a rare genetic disease improved significantly after treatment with cornstarch and glycyrrhizin.

## Contribution

A novel treatment combination of oral cornstarch and glycyrrhizin is proposed for severe liver injury in GSD type IXa.

## Key findings

- Nightly oral cornstarch and glycyrrhizin significantly improved liver injury in a patient with GSD type IXa.
- Cornstarch may help reduce glycogen buildup in the liver, while glycyrrhizin may reduce mitochondrial damage.
- GSD type IXa typically has a good prognosis, but some patients may develop fibrosis or adenomas.

## Abstract

A previously healthy 18-month-old boy presented with hepatomegaly, accompanied by liver injury. Imaging and liver biopsy findings suggested a hepatic glycogen storage disease (GSD) but not GSD type I. Genetic testing revealed a partial deletion of the PHKA2 gene, confirming the diagnosis of GSD type IXa. Initial treatment included ursodeoxycholic acid and portioned meals. However, the boy’s liver injury continued to worsen. Subsequently, nightly oral cornstarch after meals and oral glycyrrhizin were introduced. Following the addition of cornstarch and glycyrrhizin, the patient’s liver injury significantly improved. Liver injury caused by GSD is likely due to excessive glycogen accumulation in the hepatocytes. However, the detailed mechanism is unclear, particularly the minimal inflammatory cell infiltration observed in this case. While GSD IX has a good prognosis and resolves spontaneously, some patients develop hepatic fibrosis and adenomas. Cornstarch supplementation is a mainstay treatment for GSD to prevent hypoglycemia. It may also contribute to improved liver function by moderating glycogen buildup. The glycyrrhizin has also shown potential in reducing mitochondrial damage via another mechanism in this case, but additional research is warranted.

## Linked entities

- **Genes:** PHKA2 (phosphorylase kinase regulatory subunit alpha 2) [NCBI Gene 5256]
- **Chemicals:** glycyrrhizin (PubChem CID 14982), ursodeoxycholic acid (PubChem CID 31401)
- **Diseases:** Glycogen Storage Disease Type IXa (MONDO:0010598)

## Full-text entities

- **Genes:** PHKA2 (phosphorylase kinase regulatory subunit alpha 2) [NCBI Gene 5256] {aka GSD9A, PHK, PYK, PYKL, XLG, XLG2}
- **Diseases:** hepatomegaly (MESH:D006529), GSD type IXa (MESH:D006009), hypoglycemia (MESH:D007003), Liver Injury (MESH:D017093), GSD (MESH:D006008), adenomas (MESH:D000236), inflammatory (MESH:D007249), GSD type I. (MESH:D005953), hepatic fibrosis (MESH:D008103), mitochondrial damage (MESH:D028361)
- **Chemicals:** glycogen (MESH:D006003), Glycyrrhizin (MESH:D019695), ursodeoxycholic acid (MESH:D014580), Cornstarch (MESH:D013213)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC11880634/full.md

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Source: https://tomesphere.com/paper/PMC11880634