# Micronutrient Deficiencies in the Era of Second-Generation Incretin-Based Therapies for Obesity

**Authors:** Andrijana Koceva, Andrej Janež, Tajda Pečko, Mojca Jensterle

PMC · DOI: 10.3390/nu18040677 · Nutrients · 2026-02-19

## TL;DR

This review discusses how second-generation obesity drugs may affect micronutrient levels in people with obesity, who are already at risk for nutritional deficiencies.

## Contribution

The paper provides a comprehensive overview of micronutrient risks associated with incretin-based therapies and suggests strategies for nutritional monitoring.

## Key findings

- Obesity is associated with a high prevalence of baseline nutritional inadequacy.
- Incretin-based therapies may reduce dietary intake and alter micronutrient exposure.
- Risk-stratified nutritional monitoring is recommended during these therapies.

## Abstract

Second-generation incretin-based therapies have transformed the pharmacological management of obesity by inducing substantial and sustained weight loss. The weight-reducing effects are primarily mediated through appetite suppression, reduced energy intake, and modulation of eating behavior. While therapeutically beneficial, these mechanisms may also influence dietary quality, micronutrient exposure, and overall nutritional status, particularly in individuals with obesity, a population already characterized by a high prevalence of baseline nutritional inadequacy. This narrative review is intended to inform clinicians, clinical nutrition specialists and researchers involved in obesity management by summarizing baseline micronutrient vulnerability in obesity, synthesizing available evidence on dietary intake, biochemical micronutrient status, and nutrition-related clinical outcomes during incretin-based therapy, discussing plausible mechanisms linking these therapies to micronutrient risk, and outlining approaches to risk-stratified nutritional monitoring in clinical practice.

## Linked entities

- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Genes:** AGRP (agouti related neuropeptide) [NCBI Gene 181] {aka AGRT, ART, ASIP2}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, NPY (neuropeptide Y) [NCBI Gene 4852] {aka PYY4}, GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], HAMP (hepcidin antimicrobial peptide) [NCBI Gene 57817] {aka HEPC, HFE2B, LEAP1, PLTR}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}
- **Diseases:** fat malabsorption (MESH:D008286), polycystic ovary syndrome (MESH:D011085), Nutritional Deficiency (MESH:D044342), Micronutrient Deficiencies (MESH:D007153), anemia (MESH:D000740), injury to (MESH:D014947), vitamin B deficiencies (MESH:D014804), gastrointestinal symptoms (MESH:D012817), inflammation (MESH:D007249), Pancreatic exocrine insufficiency (MESH:D010188), sarcopenia (MESH:D055948), steatotic liver disease (MESH:D008107), thiamine deficiency (MESH:D013832), Zinc deficiency (MESH:C564286), micronutrient abnormality (MESH:D000014), Dehydration (MESH:D003681), Vitamin deficiency (MESH:D014802), weight loss (MESH:D015431), adverse (MESH:D064420), binge (MESH:D002032), Wernicke encephalopathy (MESH:D014899), gastrointestinal adverse events (MESH:D002318), gastrointestinal adverse effects (MESH:D005767), micronutrient insufficiency (MESH:D000309), volume depletion (MESH:C536350), overweight (MESH:D050177), diarrhea (MESH:D003967), constipation (MESH:D003248), Vitamin D deficiency (MESH:D014808), appetite (MESH:D001068), mineral deficiencies (MESH:C537337), type 2 diabetes (MESH:D003924), vitamin C deficiency (MESH:D001206), nausea, vomiting (MESH:D020250), nausea (MESH:D009325), Obesity (MESH:D009765), iron deficiency (MESH:D000090463), vomiting (MESH:D014839), morbid obesity (MESH:D009767), dyspepsia (MESH:D004415), metabolic dysfunction (MESH:D008659), iron deficiency anemia (MESH:D018798)
- **Chemicals:** 25-hydroxyvitamin D (MESH:C104450), potassium (MESH:D011188), pyridoxine (MESH:D011736), zinc (MESH:D015032), B6 (-), carbonated (MESH:D002254), vitamin D (MESH:D014807), simple sugars (MESH:D009005), carbohydrate (MESH:D002241), selenium (MESH:D012643), choline (MESH:D002794), thiamine (MESH:D013831), chromium (MESH:D002857), Iron (MESH:D007501), cobalamin (MESH:D014805), RA (MESH:D011883), B12 (MESH:C034730), carotenoid (MESH:D002338), Metformin (MESH:D008687), manganese (MESH:D008345), magnesium (MESH:D008274), folate (MESH:D005492), calcium (MESH:D002118), vitamin C (MESH:D001205), B9 (MESH:C014499)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943190/full.md

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Source: https://tomesphere.com/paper/PMC12943190