# Case Report: Conventional therapy versus volanesorsen in two sisters with familial chylomicronemia syndrome

**Authors:** Javier Vega, Benjamín Torres, Alberto Maiz, José L. Santos

PMC · DOI: 10.3389/fnut.2026.1749264 · Frontiers in Nutrition · 2026-02-09

## TL;DR

Two sisters with a rare genetic disorder had better outcomes with a new drug called volanesorsen compared to traditional treatment.

## Contribution

This case report highlights the effectiveness of volanesorsen in treating familial chylomicronemia syndrome and addresses access challenges in low-resource settings.

## Key findings

- Volanesorsen combined with nutritional counseling significantly reduced triglyceride levels and improved quality of life.
- Conventional therapy failed to control triglycerides and led to repeated hospitalizations.
- Access to advanced therapies like volanesorsen is limited in low-to-middle-income regions due to cost and insurance barriers.

## Abstract

Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder characterized by severe hypertriglyceridemia and caused by mutations in genes involved in chylomicron metabolism. Dietary management includes a very-low-fat diet, restriction of simple carbohydrates and alcohol, supplementation with medium-chain triglycerides, essential fatty acids, and fat-soluble vitamins; however, long-term adherence is often poor and nutritional therapy alone is insufficient. We report two adult Chilean sisters with FCS caused by the homozygous Q97X mutation in the APOA5 gene. Both patients experienced severe hypertriglyceridemia (>5,000 mg/dL) and recurrent episodes of acute pancreatitis. One sister was treated with volanesorsen, an antisense oligonucleotide, receiving a weekly dose of 285 mg, which was repeated every 3 weeks due to thrombocytopenia. When combined with structured nutritional counseling, pharmacological treatment achieved a marked reduction in plasma triglycerides to <250 mg/dL and a substantial improvement in quality of life. The other sister was managed with conventional therapy due to a lack of health insurance coverage for volanesorsen. She presented persistent hypertriglyceridemia and recurrent hospitalizations, underscoring the challenges of access to advanced therapies in limited-resource settings. While volanesorsen offers a promising therapeutic alternative, equitable access remains a critical issue, particularly in health systems of low-to middle-income regions.

## Linked entities

- **Genes:** APOA5 (apolipoprotein A5) [NCBI Gene 116519]
- **Diseases:** familial chylomicronemia syndrome (MONDO:0009387), acute pancreatitis (MONDO:0006515)

## Full-text entities

- **Genes:** GPIHBP1 (glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1) [NCBI Gene 338328] {aka GPI-HBP1, HYPL1D}, LMF1 (lipase maturation factor 1) [NCBI Gene 64788] {aka C16orf26, HMFN1876, JFP11, TMEM112, TMEM112A}, APOA5 (apolipoprotein A5) [NCBI Gene 116519] {aka APOAV, RAP3}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, APOC2 (apolipoprotein C2) [NCBI Gene 344] {aka APO-CII, APOC-II}, APOC3 (apolipoprotein C3) [NCBI Gene 345] {aka APOCIII, Apo-C3, ApoC-3}, LPL (lipoprotein lipase) [NCBI Gene 4023] {aka HDLCQ11, LIPD}
- **Diseases:** myocardial infarction (MESH:D009203), thrombocytopenia (MESH:D013921), hypertension (MESH:D006973), hypothyroidism (MESH:D007037), atherosclerotic vascular disease (MESH:D050197), erythema (MESH:D004890), Familial chylomicronemia syndrome (MESH:D008072), cognitive dysfunction (MESH:D003072), hypertriglyceridemia (MESH:D015228), memory loss (MESH:D008569), type 2 diabetes (MESH:D003924), paresthesia (MESH:D010292), allergic reactions (MESH:D004342), renal failure (MESH:D051437), irritability (MESH:D001523), diabetes (MESH:D003920), abdominal pain (MESH:D015746), acute pancreatitis (MESH:D010195), lipemia retinalis (MESH:D006949), dyslipidemia (MESH:D050171), eruptive xanthomas (MESH:D014973), autosomal recessive disease (MESH:D030342), pruritus (MESH:D011537)
- **Chemicals:** niacin (MESH:D009525), MSG (MESH:D012970), starches (MESH:D013213), pravastatin (MESH:D017035), gemfibrozil (MESH:D015248), carbohydrates (MESH:D002241), TCV (-), saxagliptin (MESH:C502994), TG (MESH:D013866), orlistat (MESH:D000077403), alcohol (MESH:D000438), simvastatin (MESH:D019821), glucose (MESH:D005947), lipid (MESH:D008055), fibrates (MESH:D058607), omega-3 fatty acids (MESH:D015525), triglyceride (MESH:D014280), essential fatty acids (MESH:D005228), fat (MESH:D005223), sugars (MESH:D000073893), ezetimibe (MESH:D000069438), fenofibrate (MESH:D011345), oligonucleotide (MESH:D009841), ciprofibrate (MESH:C019304), cholesterol (MESH:D002784), Volanesorsen (MESH:C000593612), metformin (MESH:D008687), acipimox (MESH:C027696)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Q97X

## Full text

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## Figures

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## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927495/full.md

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Source: https://tomesphere.com/paper/PMC12927495