# Unusual Micronutrient Deficiencies as Causes of Anemia

**Authors:** Ananya Datta Mitra, Ralph Green

PMC · DOI: 10.3390/nu18040664 · Nutrients · 2026-02-18

## TL;DR

This paper discusses how rare micronutrient deficiencies, like certain B vitamins and minerals, can cause anemia that is hard to treat and often overlooked.

## Contribution

The paper highlights the under-recognized role of uncommon micronutrient deficiencies in causing anemia.

## Key findings

- Micronutrient deficiencies like B-group vitamins, pyridoxine, and thiamine can cause anemia.
- Deficiencies in fat-soluble vitamins A and E, and trace elements like copper, zinc, and selenium also contribute to anemia.
- These deficiencies are often difficult to diagnose and may coexist with more common causes of anemia.

## Abstract

Anemia due to micronutrient deficiencies has received little attention in public health and modern-day clinical practice. Increasing numbers of persons, mainly in low- and middle-income nations, are faced with malnutrition and malabsorption syndromes, giving rise to various micronutrient deficiencies that can lead to anemias refractory to treatment with iron, folate or vitamin B12. Though relatively uncommon, such underlying nutrient deficiencies may be difficult to recognize as they can coexist with more common causes and there may be few or no specific clinical characteristics pinpointing a particular micronutrient. The main examples of these micronutrients contributing to a small but important burden of anemia are other B-group vitamins, pyridoxine and thiamine, ascorbic acid, the fat-soluble vitamins, A and E and other trace elements such as copper, zinc and selenium. The following review highlights the current state of knowledge and the relevance of these micronutrient deficiencies in the broader context of nutritional anemia.

## Linked entities

- **Chemicals:** pyridoxine (PubChem CID 1054), thiamine (PubChem CID 1130), ascorbic acid (PubChem CID 9888239), vitamin A (PubChem CID 445354), vitamin E (PubChem CID 14985), copper (PubChem CID 23978), zinc (PubChem CID 23994), selenium (PubChem CID 6326970)
- **Diseases:** anemia (MONDO:0002280)

## Full-text entities

- **Genes:** HEPH (hephaestin) [NCBI Gene 9843] {aka CPL}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}, GSR (glutathione-disulfide reductase) [NCBI Gene 2936] {aka CNSHA10, GR, GSRD, HEL-75, HEL-S-122m}, SLC11A2 (solute carrier family 11 member 2) [NCBI Gene 4891] {aka AHMIO1, DCT1, DMT1, NRAMP2}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, SLC19A1 (solute carrier family 19 member 1) [NCBI Gene 6573] {aka CHMD, FOLT, IFC-1, IFC1, IMD114, MEGAF}, SLC40A1 (solute carrier family 40 member 1) [NCBI Gene 30061] {aka FPN, FPN1, HFE4, IREG1, MST079, MSTP079}, DHFR (dihydrofolate reductase) [NCBI Gene 1719] {aka DHFR1, DYR}, LOX (lysyl oxidase) [NCBI Gene 4015] {aka AAT10}, TMPRSS6 (transmembrane serine protease 6) [NCBI Gene 164656] {aka IRIDA, MT2}, HAMP (hepcidin antimicrobial peptide) [NCBI Gene 57817] {aka HEPC, HFE2B, LEAP1, PLTR}, DBH (dopamine beta-hydroxylase) [NCBI Gene 1621] {aka DBM, ORTHYP1}, SLC19A3 (solute carrier family 19 member 3) [NCBI Gene 80704] {aka BBGD, THMD2, THTR2, hTHTR2, thTr-2}, SLC19A2 (solute carrier family 19 member 2) [NCBI Gene 10560] {aka TC1, THMD1, THT1, THTR1, TRMA}, CP (ceruloplasmin) [NCBI Gene 1356] {aka AB073614, CP-2}
- **Diseases:** Vitamin B6 Deficiency (MESH:D026681), edema (MESH:D004487), acrodermatitis enteropathica (MESH:C538178), osteoporosis (MESH:D010024), Vitamin A deficiency (MESH:D014802), cystic fibrosis (MESH:D003550), nephrosis (MESH:D009401), immunologic abnormalities (MESH:D007154), polyneuropathy (MESH:D011115), diabetes mellitus (MESH:D003920), bile duct obstruction (MESH:D002779), thrombocytopenia (MESH:D013921), hereditary hemolytic anemias (MESH:D000745), parasitic infestations (MESH:D007239), hemoglobinopathies (MESH:D006453), exudative enteropathies (MESH:D011504), growth retardation (MESH:D006130), pellagra (MESH:D010383), deficiency of folate (MESH:C562799), alcoholics (MESH:D000437), glucose-6-phosphate dehydrogenase deficiency (MESH:D005955), pure red cell aplasia (MESH:D012010), neutropenia (MESH:D009503), malnourished (MESH:D044342), Micronutrient Deficiencies (MESH:D007153), Pantothenic Acid Deficiency (MESH:D006211), death (MESH:D003643), hematologic abnormalities (MESH:D006402), fractures of the submetaphysis (MESH:D050723), altered taste sensation (MESH:D004408), myeloid arrest (MESH:D007951), malabsorption (MESH:D008286), scurvy (MESH:D012614), Zinc deficiency (MESH:C564286), sideroblastic anemias (MESH:D000756), Thiamine Deficiency (MESH:D013832), Trace Metal Deficiencies (MESH:D013651), steatorrhea (MESH:D045602), iron overload (MESH:D019190), Pelger-Huett-like anomaly (MESH:C564899), Inflammatory (MESH:D007249), Vitamin E deficiency (MESH:D014811), pancreatic insufficiency (MESH:D010188), cerebellar ataxia (MESH:D002524), short bowel syndrome (MESH:D012778), dietary hemosiderosis (MESH:D006486), rib fractures (MESH:D012253), Anemia (MESH:D000740), injury to (MESH:D014947), hemolysis (MESH:D006461), iron (MESH:D000090463), thalassemia (MESH:D013789), celiac disease (MESH:D002446), hypochromic anemia (MESH:D000747), Wilson disease (MESH:D006527), Deficiencies of specific micronutrients (MESH:D000080888), iron deficiency anemia (MESH:D018798), degeneration of the spinal cord (MESH:D013118), proteinuria (MESH:D011507), reticulocytosis (MESH:D045262)
- **Chemicals:** Desferal (MESH:D003676), Selenium (MESH:D012643), aminolevulinic acid (MESH:D000622), tocopherol (MESH:D024505), 51Cr (MESH:C000615375), Riboflavin (MESH:D012256), heme (MESH:D006418), Vitamin E (MESH:D014810), Thiamine (MESH:D013831), niacin (MESH:D009525), bilirubin (MESH:D001663), oxalate (MESH:D010070), Isoniazid (MESH:D007538), pyridoxine (MESH:D011736), copper sulfate (MESH:D019327), 5-methyltetrahydrofolate (MESH:C005984), Zinc (MESH:D015032), polyunsaturated fatty acid (MESH:D005231), vitamin D (MESH:D014807), 10-formylfolate (-), Folate (MESH:D005492), ROS (MESH:D017382), Pyridoxal phosphate (MESH:D011732), Ascorbate (MESH:D001205), Copper (MESH:D003300), vitamin B6 (MESH:D025101), galactoflavin (MESH:C007811), alpha-tocopherol (MESH:D024502), Vitamin A (MESH:D014801), Vitamin B12 (MESH:D014805), Iron (MESH:D007501), lipid (MESH:D008055), copper chloride (MESH:C029892), tetrahydrofolate (MESH:C030371), pantothenic acid (MESH:D010205), water (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Cavia porcellus (domestic guinea pig, species) [taxon 10141]

## Full text

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## References

104 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943217/full.md

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Source: https://tomesphere.com/paper/PMC12943217