# Mineral disorders after hematopoietic stem cell transplantation in patients receiving parenteral nutrition

**Authors:** Taís Daiene Russo Hortencio, Julia Daudt de Faro Salamonde, Alice Missagia de Mattos Springer, Afonso Celso Vigorito, Vitória de Andrade Mendonça, Roberto José Negrão Nogueira

PMC · DOI: 10.1016/j.htct.2026.106353 · Hematology, Transfusion and Cell Therapy · 2026-03-21

## TL;DR

This study examines how common mineral deficiencies are in patients receiving parenteral nutrition after stem cell transplants.

## Contribution

The study provides new insights into the prevalence of specific mineral disorders during the engraftment period in this patient population.

## Key findings

- Hypomagnesemia was the most prevalent mineral disorder, affecting 50.0–62.3% of patients.
- Hypophosphatemia and hypokalemia were also common, with prevalence rates of 21.1–40.3% and 10.5–31.2%, respectively.
- Severe mineral disorders were observed in only a small proportion of patients.

## Abstract

Parenteral nutrition is a critical therapeutic approach for patients undergoing hematopoietic stem cell transplantation. However, parenteral nutrition is associated with complications such as mineral disorders. This study evaluated the prevalence of hypophosphatemia, hypokalemia, and hypomagnesemia in adult transplant patients before and within the first 24 days of parenteral nutrition infusion.

This retrospective cohort study included patients who underwent hematopoietic stem cell transplantation and required parenteral nutrition at a public quaternary hospital in Brazil between January 2012 and January 2022. Patients were categorized based on indications for parenteral nutrition and specific diagnoses. Laboratory monitoring of phosphorus, potassium, and magnesium levels was performed at predefined intervals during parenteral nutrition infusion, starting at 72 h and during subsequent 4-day intervals until engraftment. Hypophosphatemia, hypokalemia, and hypomagnesemia were defined as levels below established reference values. Descriptive analyses were applied, and the chi-square test, crude odds ratios, and Fisher's exact test were used to compare categorical variables between the periods.

The study revealed varying prevalences of hypophosphatemia (21.1–40.3 %), hypokalemia (10.5–31.2 %), and hypomagnesemia (50.0–62.3 %) among the 77 patients included in the study. Severe mineral disorders were observed in only a small proportion of patients.

Patients undergoing hematopoietic stem cell transplantation had a high prevalence of mineral depletion throughout the engraftment period.

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, TRPM6 (transient receptor potential cation channel subfamily M member 6) [NCBI Gene 140803] {aka CHAK2, HMGX, HOMG, HOMG1, HSH}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, TTR (transthyretin) [NCBI Gene 7276] {aka AMYLD1, ATTR, CTS, CTS1, HEL111, HsT2651}
- **Diseases:** depleted (MESH:C536350), overweight (MESH:D050177), myeloid malignancies (MESH:D009369), acute kidney injury (MESH:D058186), Mineral disorders (MESH:D012080), neuromuscular disturbances (MESH:D009468), Refeeding syndrome (MESH:D055677), Hypophosphatemia (MESH:D017674), cardiac arrhythmias (MESH:D001145), Theft syndrome (MESH:D013577), mineral disturbances (MESH:C537337), inflammation (MESH:D007249), hypomagnesemia (OMIM:613882), Graft-versus-host disease (MESH:D006086), Mucositis (MESH:D052016), Electrolyte disturbances (MESH:D014883), necrotic (MESH:D009336), neutropenic colitis (MESH:D003092), anorexia (MESH:D000855), lymphoid malignancies (MESH:D008223), amyloidosis (MESH:D000686), death (MESH:D003643), NMTT (MESH:D044342), obese (MESH:D009765), polycythemia (MESH:D011086), hypoalbuminemia (MESH:D034141), ulceration (MESH:D014456), infections (MESH:D007239), tubulopathy (MESH:C557674), respiratory distress (MESH:D012128), aplastic anemia (MESH:D000741), hematological diseases (MESH:D006402), Hypokalemia (MESH:D007008), neutropenia (MESH:D009503)
- **Chemicals:** amino acids (MESH:D000596), magnesium (MESH:D008274), sodium (MESH:D012964), creatinine (MESH:D003404), Phosphorus (MESH:D010758), glucose (MESH:D005947), urea (MESH:D014508), nitrogen (MESH:D009584), carbohydrates (MESH:D002241), chloride (MESH:D002712), calcium (MESH:D002118), cholesterol (MESH:D002784), triglycerides (MESH:D014280), potassium (MESH:D011188), lipids (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC13022652/full.md

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Source: https://tomesphere.com/paper/PMC13022652