# Changes in anemia prevalence and the proportion of anemia associated with iron deficiency or inflammation in young children residing in Puno, Peru: Analysis using new World Health Organization guidelines for defining anemia

**Authors:** Cinthya Vásquez-Velásquez, Benita Maritza Choque-Quispe, Parminder S. Suchdev, Chris A. Rees, Vilma Tapia, Yi-An Ko, Gustavo F. Gonzales, Raquel Inocencio da Luz, Raquel Inocencio da Luz, Raquel Inocencio da Luz, Raquel Inocencio da Luz, Raquel Inocencio da Luz

PMC · DOI: 10.1371/journal.pone.0342255 · PLOS One · 2026-02-20

## TL;DR

New WHO guidelines for diagnosing anemia in young children in Puno, Peru, reduced anemia prevalence estimates, but most cases were still linked to inflammation rather than iron deficiency.

## Contribution

The study evaluates the impact of new WHO anemia guidelines on prevalence and etiology in a high-altitude region of Peru.

## Key findings

- Anemia prevalence decreased from 50% to 42.2% under new WHO guidelines.
- Inflammation was the leading cause of anemia (45.9%), followed by iron deficiency (27.5%).
- Iron deficiency remained significantly associated with anemia in adjusted analyses.

## Abstract

In 2024, the World Health Organization (WHO) introduced new hemoglobin cutoffs for diagnosing anemia. The WHO also incorporated revised altitude adjustments and lowered thresholds to diagnose anemia for children aged 6–23 months. Puno, Peru has historically reported the highest prevalence of anemia in the country, exceeding 70% in infants and young children.

To assess the impact of the new WHO cutoffs on anemia prevalence and evaluate whether they affected the proportion of anemia attributable to iron deficiency (ID), inflammation, and other causes.

A cross-sectional study was conducted among 310 children aged 6–59 months in Puno, Peru. Participants were recruited via convenience sampling during routine medical check-ups. Venous blood samples were analyzed using an automated hemoglobin analyzer and serum biomarker evaluations. Anemia prevalence was determined based on WHO guidelines for children aged 6−59 months (and 6−23 months and 24−59 months as subgroups). The ratio of anemia due to ID (Ferritin <12 ng/mL) or inflammation (IL-6 > 60 pg/mL) was estimated using adjusted Poisson regression models, reporting prevalence ratios (PR).

Applying the new WHO guidelines, anemia prevalence changed from 50% to 42.2% in children aged 6−59 months (62% to 47% in children aged 6−23 months and from 45.9% to 40.6% in children aged 24−59 months). The proportion of anemia due to ID was 27.5%, due to inflammation was 45.9%, and due to other causes was 26.6%. ID was significantly associated with anemia in both unadjusted and adjusted analyses (PR: 1.4, 95% CI: 1.1–1.8; PR: 1.32, 95% CI: 1.0–1.7). The 2024 WHO guidelines did not substantially alter the estimated proportion of anemia associated with ID or inflammation.

Application of the new WHO cutoffs resulted in a lower estimated prevalence of anemia among young children. ID accounted for only a small proportion of cases of anemia, emphasizing the need for further research into other causes of childhood anemia in Peru.

## Linked entities

- **Diseases:** anemia (MONDO:0002280)
- **Species:** Peru (taxon 1767537)

## Full-text entities

- **Genes:** TFRC (transferrin receptor) [NCBI Gene 7037] {aka CD71, IMD46, T9, TFR, TFR1, TR}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, EPO (erythropoietin) [NCBI Gene 2056] {aka DBAL, ECYT5, EP, MVCD2}, HAMP (hepcidin antimicrobial peptide) [NCBI Gene 57817] {aka HEPC, HFE2B, LEAP1, PLTR}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}
- **Diseases:** Anemia (MESH:D000740), nutritional deficiencies (MESH:D044342), micronutrient deficiencies (MESH:D007153), infection (MESH:D007239), CRED (MESH:C562515), deficiencies of other vitamins (MESH:D058497), diseases (MESH:D004194), Inflammation (MESH:D007249), hereditary disorders (MESH:D009386), AF (MESH:D020969), hemoglobinopathies (MESH:D006453), TBI (MESH:D000070642), genetic disorders (MESH:D030342), IDA (MESH:D018798), thalassemia (MESH:D013789), ID (MESH:D000090463)
- **Chemicals:** PONE-D-25-18153 (-), beta-carotene (MESH:D019207), calcium (MESH:D002118), folate (MESH:D005492), oxygen (MESH:D010100), zinc (MESH:D015032), Iron (MESH:D007501), vitamin A (MESH:D014801), ascorbic acid (MESH:D001205)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** Line 231 — Mus musculus (Mouse), Hybridoma (CVCL_L524)

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12923139/full.md

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Source: https://tomesphere.com/paper/PMC12923139