# Are protein substitutes available in Italy for infants with inherited metabolic diseases all the same?

**Authors:** Margherita Di Costanzo, Martina Tosi, Martina Muzi, Enrico Vito Buono, Valentina D’Onghia, Anna Munerati, Gabriele Tarditi, Simone Bruni, Elvira Verduci, Giacomo Biasucci

PMC · DOI: 10.3389/fnut.2025.1581295 · Frontiers in Nutrition · 2025-05-26

## TL;DR

This study compares infant protein substitutes in Italy for inherited metabolic diseases, highlighting differences in nutritional content that could affect health outcomes.

## Contribution

The first comprehensive comparison of infant protein substitutes for inherited metabolic diseases on the Italian market.

## Key findings

- Some protein substitutes exceed energy and fatty acid levels while lacking key micronutrients like vitamin D and iodine.
- All products contain DHA and EPA, but only half contain ARA.
- The study identifies potential areas for improving nutritional adequacy in these specialized formulas.

## Abstract

Inherited metabolic diseases (IMDs) represent a major clinical challenge, especially during the neonatal and infant periods. They require tailored and long-term nutritional management to ensure proper growth and development. Protein substitutes are essential in the dietary treatment of IMDs, particularly aminoacidopathies, organic acidemias, and urea cycle disorders. In Italy, a variety of PSs is available for infants with IMDs requiring a controlled protein and/or amino acid intake; however, differences in their nutritional composition may impact clinical outcomes. This study aims to examine and compare the nutritional composition of infant PSs (IPSs) available on the Italian market, focusing on macronutrients, micronutrients, and functional components.

The analysis targets products used in the dietary management of aminoacidopathies, organic acidemias, and urea cycle disorders during the first year of life. We compared the nutritional composition of products intended for healthy infants, considering the Commission Delegated Regulation (EU) 2016/127 and Commission Delegated Regulation (EU) 2016/128. Phenylketonuria is excluded from this analysis, as it has been recently addressed in another paper.

For each condition, there are only two products available, except for isovaleric aciduria and urea cycle disorders, which have only one product. The results indicate higher energy, linoleic, and alpha-linolenic acid content (+9%, +55%, and +290% compared to the maximum reference value), and lower levels of lactose, vitamin D, choline, selenium, and iodine (−92%, −34%, −37%, −12%, and −39% compared to the minimum reference value) for several IPSs. The analysis revealed the presence of docosahexaenoic acid (DHA), and eicosapentaenoic acid (EPA) in all IPSs, while half of them contain arachidonic acid (ARA).

This study represents the first comprehensive comparison of the nutritional profiles of IPSs for IMDs on the Italian market. The results identify potential areas for optimization, aiming to provide adequate levels of micronutrients, essential fatty acids, and functional ingredients, such as biotics, to support gut health, immune function, and neurodevelopment.

## Linked entities

- **Diseases:** urea cycle disorders (MONDO:0004739), phenylketonuria (MONDO:0009861)

## Full-text entities

- **Diseases:** Phenylketonuria (MESH:D010661), isovaleric aciduria (MESH:C538167), organic acidemias (MESH:D000092124), IMDs (MESH:D030342), urea cycle disorders (MESH:D056806)
- **Chemicals:** ARA (MESH:D016718), vitamin D (MESH:D014807), EPA (MESH:D015118), linoleic (-), choline (MESH:D002794), selenium (MESH:D012643), essential fatty acids (MESH:D005228), alpha-linolenic acid (MESH:D017962), DHA (MESH:D004281), amino acid (MESH:D000596), lactose (MESH:D007785), iodine (MESH:D007455)

## Full text

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12146189/full.md

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Source: https://tomesphere.com/paper/PMC12146189