# Prevalence of Vitamin D Deficiency and Its Association With Anemia Severity in Anemic Patients: A Cross-Sectional Study

**Authors:** Aby Aurthur Michael, Aswathy P T, Deepthi Krishnan

PMC · DOI: 10.7759/cureus.103157 · Cureus · 2026-02-07

## TL;DR

This study finds that vitamin D deficiency is common among anemic patients in India and is linked to the severity of anemia, though not directly to hemoglobin levels.

## Contribution

The study reports a novel association between vitamin D status and anemia severity in a clinical setting in South India.

## Key findings

- Vitamin D deficiency was present in 40.7% of anemic patients.
- Vitamin D status was significantly associated with anemia severity (p = 0.003).
- Iron deficiency anemia was the most common type among the studied population.

## Abstract

Background

Vitamin D deficiency remains highly prevalent in India, even though the population is exposed to abundant sunlight throughout most of the year. However, data evaluating vitamin D status specifically among anemic adult populations in routine clinical settings remain limited. This study was undertaken to determine the prevalence of vitamin D deficiency in patients with anemia and to examine its relationship with hemoglobin concentration, the severity of anemia, and the underlying anemia subtype.

Methods

This cross-sectional, hospital-based observational study was conducted over six months in the department of general medicine at a tertiary care center in South India. A total of 246 anemic patients (hemoglobin <11 g/dL) aged >13 years were enrolled after obtaining informed consent. Demographic data, body mass index (BMI), sun exposure duration, skin type, and dietary vitamin D intake were recorded. Laboratory evaluation comprised measurement of hemoglobin concentration, serum ferritin, total iron-binding capacity (TIBC), C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), and serum 25-hydroxyvitamin D levels. Vitamin D status was defined based on serum 25-hydroxyvitamin D concentrations and categorized as deficient (<20 ng/mL), insufficient (20-29 ng/mL), or sufficient (≥30 ng/mL). Anemia was subsequently categorized according to both severity and etiological type.

Results

The mean age of the patients was 45.31 ± 18.27 years, with females constituting 156 participants (63.4%). The mean hemoglobin concentration was 8.68 ± 1.81 g/dL. Based on severity, moderate anemia was most common, observed in 121 patients (49.2%), followed by mild anemia in 87 (35.4%) and severe anemia in 38 (15.4%). Iron deficiency anemia was the predominant anemia type, identified in 165 patients (67.1%), while anemia of chronic disease and megaloblastic anemia were present in 71 (28.9%) and 10 patients (4.1%), respectively. The mean serum 25-hydroxyvitamin D level was 23.71 ± 12.00 ng/mL. Vitamin D deficiency was noted in 100 patients (40.7%) and insufficiency in 76 patients (30.9%), resulting in an overall prevalence of suboptimal vitamin D status in 176 patients (71.6%). Mean hemoglobin levels differed significantly across vitamin D status categories (ANOVA, p = 0.017) and dietary vitamin D intake categories (ANOVA, p = 0.008). Analysis revealed a statistically significant association between vitamin D status and the severity of anemia (χ² = 16.01, p = 0.003). In contrast, vitamin D status showed no significant relationship with the etiological classification of anemia (p = 0.531). Similarly, dietary vitamin D intake was not significantly associated with either anemia severity or anemia type. Pearson’s correlation analysis indicated the absence of a meaningful linear relationship between serum vitamin D concentrations and hemoglobin levels (r = 0.050, p = 0.434).

Conclusion

Vitamin D deficiency is highly prevalent among anemic patients. Although serum vitamin D levels did not show a significant linear correlation with hemoglobin concentration, categorical vitamin D status was associated with anemia severity in a non-linear manner, highlighting the potential clinical relevance of vitamin D status in anemic populations.

## Linked entities

- **Diseases:** anemia (MONDO:0002280), iron deficiency anemia (MONDO:0001356), anemia of chronic disease (MONDO:0020725), megaloblastic anemia (MONDO:0001700)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, HAMP (hepcidin antimicrobial peptide) [NCBI Gene 57817] {aka HEPC, HFE2B, LEAP1, PLTR}, PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}
- **Diseases:** osteoporosis (MESH:D010024), hematological disorders (MESH:D006402), Anemia (MESH:D000740), Anemia of chronic disease (MESH:D002908), cardiovascular and infectious diseases (MESH:D003141), multiple sclerosis (MESH:D009103), aplastic anemia (MESH:D000741), hemolytic anemia (MESH:D000743), sickle cell anemia (MESH:D000755), type 1 diabetes mellitus (MESH:D003922), megaloblastic anemia (MESH:D000749), underweight (MESH:D013851), depression (MESH:D003866), skin pigmentation (MESH:D010859), extra-skeletal disorders (MESH:D000092225), chronic kidney disease (MESH:D051436), schizophrenia (MESH:D012559), neuropsychiatric disorders (MESH:D001523), insufficiency (MESH:D000309), malignancy (MESH:D009369), fractures (MESH:D050723), respiratory illnesses (MESH:D012140), Fitzpatrick skin type V (MESH:D012871), chronic liver disease (MESH:D008107), anemia of inflammation (MESH:D007249), thalassemia (MESH:D013789), iron deficiency (MESH:D000090463), myelodysplastic syndromes (MESH:D009190), Iron deficiency anemia (MESH:D018798), chronic obstructive pulmonary disease (MESH:D029424), overweight (MESH:D050177), ACD (MESH:C535474), Vitamin D Deficiency (MESH:D014808), autoimmune conditions (MESH:D001327), obese (MESH:D009765)
- **Chemicals:** 25-hydroxyvitamin D (MESH:C104450), 25(OH)D (-), magnesium (MESH:D008274), calcium (MESH:D002118), folic acid (MESH:D005492), vitamin B12 (MESH:D014805), steroids (MESH:D013256), phosphorus (MESH:D010758), zinc (MESH:D015032), secosteroid (MESH:D012632), Vitamin D (MESH:D014807), Iron (MESH:D007501)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12970411/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12970411/full.md

## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12970411/full.md

---
Source: https://tomesphere.com/paper/PMC12970411