High Ferritin Levels And Low Vitamin D
Original article
peer-reviewed
The Association Between Ferritin and Vitamin D Levels in Premenopausal Fibroid Uterus Cases With Anemia
Published: February 17, 2021 (see history)
DOI: 10.7759/cureus.13392
Cite this article as: Kumari S, Swetha P, Krishnan R S, et al. (February 17, 2021) The Association Between Ferritin and Vitamin D Levels in Premenopausal Fibroid Uterus Cases With Anemia. Cureus 13(2): e13392. doi:10.7759/cureus.13392
Abstract
Objective
The present study aimed to evaluate the association between serum ferritin and vitamin D levels in fibroid uterus cases presenting with anemia.
Methods
Sixty premenopausal women with uterine fibroids (30 associated with anemia and 30 without anemia) were enrolled as cases and control. All participants were evaluated on the basis of a questionnaire, which included queries related to obstetric, medical, and sociodemographic history. Peripheral blood smear, complete blood count (CBC), hemoglobin (Hb), and serum ferritin concentration were measured by a fully automated analyzer, and 25(OH) vitamin D level was measured by enzyme-linked immunosorbent assay (ELISA).
Results
There was a significant difference in ferritin levels between cases and control (p<0.001). The exposure to sunlight was moderate (one-hour exposure) in all subjects, eliminating the confounding effect of sunlight exposure influencing vitamin D levels. The median vitamin D level in cases was 5.0 ng/ml [interquartile range (IQR): 4.8], and that in control was 18.4 ng/ml (IQR: 7.9; p<0.001). A strong positive correlation of (r)=0.616 (p<0.001) was found between serum ferritin and vitamin D levels.
Conclusion
Fibroid uterus cases with anemia are more prone to vitamin D deficiency as compared to cases without anemia. Vitamin D estimation in fibroid uterus cases presenting with anemia would be useful for better patient management.
Introduction
Uterine fibroid (leiomyoma) is the most common benign tumor in the uterus, and there is a growing prevalence of fibroid uterus in India [1], which has been associated with major health and economic burden in women of reproductive age group. Fibroid uterus occurs in 20-40% of women of reproductive age, and one-third of gynecology admissions happen to be fibroids with menorrhagia, anemia, and lump in the abdomen with pain [2] severe enough to significantly impact women's quality of life. Submucosal fibroids cause severe bleeding per vagina followed by intramural type resulting in anemia [3]. Studies have highlighted vitamin D deficiency as a major risk factor for the development of uterine fibroids [4,5]. Though factors like race, ethnicity, tradition, culture, seasonal variation, exposure to sunlight, and nutritional status play a major role in regulating vitamin D levels, the cause of hypovitaminosis D in fibroids is still a topic of active research. Recently, the co-existence of anemia and hypovitaminosis D has emerged as a new causal association [6] in fibroid uterus cases, but many studies have also reported vitamin D deficiency without anemia [7,8]. Vitamin D influences iron metabolism and erythropoiesis, whereas iron is essential for vitamin D synthesis as well [9]. In terms of anemia, some studies have reported that ferritin levels are positively associated with serum vitamin D [10-12]. Though the existing scientific data indicates the role of vitamin D in fibroid uterus cases, the co-existence of anemia with vitamin D deficiency and the association between ferritin and vitamin D levels in premenopausal women with fibroid uterus are still not fully understood. The present study was conducted to estimate serum ferritin, vitamin D, and hemoglobin (Hb) levels in fibroid uterus cases presenting with anemia and to compare these values with premenopausal fibroid uterus cases presenting without anemia. Further evaluation was done to determine the association between ferritin and serum vitamin D levels in anemic and non-anemic fibroid uterus women to ascertain the correlation.
Materials & Methods
A hospital-based case-control study was conducted in the Department of Biochemistry, All India Institute of Medical Sciences, Bhubaneswar after obtaining approval from the Institute Ethical Committee. Sixty clinically diagnosed premenopausal women with uterine fibroids (30 cases with anemia and 30 cases without anemia) within the age group of 25-45 years, irrespective of their parity, who were attending the outpatient section of the Obstetrics and Gynaecology Department, and who satisfied the inclusion criteria, were enrolled randomly in this study. Post-menopausal women, women with inflammatory disorders, acute infections, and chronic liver and kidney diseases, and those with autoimmune conditions were excluded from the study.
All participants were evaluated on the basis of a questionnaire prepared pertaining to the study, which included queries related to parity, age at menarche, last menstrual period, breastfeeding, type of delivery, history of intake of oral contraceptive pills (OCPs), hormone replacement therapy, miscarriage, duration of exposure to sunlight (<1 hour/day, one hour/day, >1 hour/day), race, ethnicity, history of chronic diseases like diabetes, hypertension, renal disorders, inflammatory conditions, autoimmune disorders, history of recent blood transfusion, history of intake of multivitamin/iron supplements, and the type of nutrition. The blood pressure of the participants was recorded, and height and weight were measured to calculate their body mass index (BMI).
Biochemical analysis
After obtaining informed written consent, a 5-ml blood sample was collected from all participants. The serum was stored at -20 °C until it was used for biochemical evaluation. Peripheral blood smear, complete blood count (CBC), and Hb concentration were measured by a fully automated analyzer (AU platform) using system-compatible kits. The serum ferritin levels were estimated by three-site sandwich immunoassay using direct chemiluminometric technology in chemiluminescence immunoassay analyzer (ADVIA Centaur®, Siemens Healthineers, Erlangen, Germany). Serum vitamin D levels were estimated by enzyme-linked immunosorbent assay (ELISA) method (sandwich ELISA) using a commercial 25(OH) vitamin D ELISA Kit (Elabscience, Houston, TX) as per the manufacturer's recommendations.
Based on the data obtained from the questionnaire as well as the biochemical analysis, the patients were divided into two groups: group A: fibroid with anemia (treated as cases); group B: fibroid without anemia (treated as the control group). Subjects in the anemic group (group A) were further classified into iron deficiency anemia (Hb: <11g/dl, ferritin: <12ng/ml) and iron deficiency state (Hb: >11g/dl, ferritin: <12ng/ml). Subjects in the non-anemic group (group B) were those with Hb of >11 g/dl and ferritin of >12 ng/ml. Vitamin D status analyzed by estimating 25(OH) vitamin D levels (circulating active metabolite) in the serum was categorized as vitamin D deficiency, with 25(OH)D levels of <20ng/ml; vitamin D insufficiency, with 25(OH)D levels of 20-30 ng/ml; and vitamin D sufficiency, with 25(OH)D levels of >30 ng/ml.
Statistical analysis
The data were analyzed using the SPSS Statistics software (IBM, Armonk, NY). The Mann-Whitney U test was used for comparing the two groups. We investigated the Pearson's correlations between the hematologic parameters, i.e., ferritin and 25(OH)D levels. The odds ratio was calculated to determine the strength of association between the variables and uterine fibroids. To evaluate the odds ratio between iron deficiency anemia, iron deficiency state, and vitamin D deficiency/insufficiency subjects, the iron deficiency anemia and iron deficiency state groups, as well as the vitamin D deficiency and vitamin D insufficiency groups, were combined to form two separate groups for further analysis. Multivariate logistic regression analysis was also performed.
Results
The clinical characteristics of the study groups were evaluated (Table 1). The data was found to be non-parametric in the Kolmogorov-Smirnov test. The median ages of fibroid subjects with anemia and those without anemia were more or less the same. The median BMI of the anemic group was 22.7 kg/m2 [interquartile range (IQR): 3.6], and that of the control group was 20.3 kg/m2 (IQR-4.7, p=0.008). There was a significant difference in Hb levels between the two groups. The mean corpuscular volume (MCV), mean corpuscular Hb (MCH), and mean corpuscular Hb concentration (MCHC) also showed a significant difference between the groups (p<0.001 for each), so did the packed cell volume (PCV) (p<0.001) and red cell distribution width (p=0.037). There was no significant difference in RBC counts between cases and control (p=0.717). The median ferritin level in cases was 8.0 ng/ml (IQR: 4.1), and that in control was 47.1 ng/ml (IQR: 59), and the difference was found to be statistically significant (p<0.001). The median vitamin-D level in fibroid cases with anemia was 5.0 ng/ml (IQR: 4.8), and that in cases without anemia was 18.4 ng/ml (IQR-7.9), which also indicated a significant difference (p<0.001).
| Parameters | Fibroid subjects without anemia, median (IQR) | Fibroid subjects with anemia, median (IQR) | P-value |
| Age, years | 42.5 (10.5) | 44.0 (7.5) | 0.736 |
| BMI, kg/m2 | 20.3 (4.7) | 22.7 (3.6) | 0.008* |
| SBP, mmHg | 110.5 (10) | 113.0 (10) | 0.804 |
| DBP, mmHg | 76.0 (10) | 73.0 (10) | 1.000 |
| Hemoglobin, g/dl | 12.5 (0.8) | 9.8 (2.0) | <0.001* |
| MCV, fl/cell | 86.5 (6.1) | 75.0 (10) | <0.001* |
| MCH, pg/cell | 28.2 (1.9) | 22.5 (5.2) | <0.001* |
| MCHC, g/dl | 31.7 (1.6) | 30.2 (1.5) | <0.001* |
| RBC, million/mm3 | 4.5 (0.9) | 4.4 (1.1) | 0.717 |
| WBC, thousand cells/mm3 | 7.1 (2.7) | 7.6 (2.3) | 0.762 |
| Platelets, lakhs/mm3 | 2.8 (1.0) | 3.3 (1.4) | 0.070 |
| PCV, % | 38.1 (7.1) | 32.3 (6.3) | <0.001* |
| RDW, % | 15.2 (5.8) | 17.2 (3.0) | 0.037* |
| Urea, mg/dl | 16.5 (5.0) | 18.0 (4.0) | 0.427 |
| Creatinine, mg/dl | 0.7 (0.2) | 0.7 (0.2) | 0.694 |
| Ferritin, ng/ml | 47.1 (59.0) | 8.0 (4.1) | <0.001* |
| Vitamin D (ng/ml) | 18.4 (7.9) | 5.0 (4.8) | <0.001* |
Table 2 compares the baseline characteristics of the two groups. The comparison was done using the chi-square test. The number of fibroids or type of fibroids was more or less the same in the two groups. Obstetric parameters such as parity, history of breastfeeding, and the use of oral OCPs did not differ much between cases and controls; 70% of the cases had a microscopic hypochromic appearance in the peripheral smear, which was less for controls. Only nine (30%) had a normocytic normochromic appearance in the anemic group, but 28 (93.3%) subjects in the control group had a normal appearance. This difference was significant (p<0.001). The exposure to sunlight was moderate (one-hour exposure) in all subjects, thereby eliminating the confounding effect of sunlight exposure influencing vitamin D levels in fibroid uterus cases.
| Parameters | Fibroid subjects without anemia, n (%) | Fibroid subjects with anemia, n (%) | P-value | |
| Associated type 2 DM | 3 (10) | 3 (10) | 1.000 | |
| Associated hypertension | 0 (0) | 3 (10) | 0.237 | |
| Associated thyroid disorder | 6 (20) | 4 (13.3) | 0.551 | |
| Number of fibroids | 1 | 23 (76.7) | 17 (56.7) | 0.104 |
| 2 | 3 (10) | 1 (0.3) | ||
| 3 | 0 (0) | 1 (0.3) | ||
| Multiple | 4 (13.3) | 11 (36.7) | ||
| Type of fibroid | Submucosal | 7 (23.3) | 7 (23.3) | 0.072 |
| Intramural | 13 (43.3) | 20 (66.7) | ||
| Subserosal | 10 (30.3) | 3 (10) | ||
| Size of fibroid | <7 cm | 17 (56.7) | 18 (60) | 0.739 |
| >7 cm | 13 (43.3) | 12 (40) | ||
| Menarche | <13 years | 6 (20) | 11 (36.7) | 0.252 |
| >13 years | 24 (80) | 19 (63.3) | ||
| Parity | Nulliparous | 8 (26.7) | 4 (13.3) | 0.290 |
| Uniparous | 5 (16.7) | 9 (30) | ||
| Multiparous | 17 (56.7) | 17 (56.7) | ||
| History of breastfeeding | Yes | 21 (70) | 26 (86.7) | 0.209 |
| No | 9 (30) | 4 (13.3) | ||
| History of miscarriage | Yes | 8 (26.7) | 6 (20) | 0.761 |
| No | 22 (73.3) | 24 (80) | ||
| History of oral contraceptive pill use | Yes | 1 (3.3) | 2 (6.7) | 1.000 |
| No | 29 (96.7) | 28 (93.3) | ||
| Peripheral smear | Microcytic hypochromic | 2 (6.7) | 21 (70) | <0.001* |
| Normocytic normochromic | 28 (93.3) | 9 (30) | ||
| Exposure to sunlight | <1 hour/day, 1 hour/day, >1 hour/day | 0 (0), 30 (100), 0 (0) | 0 (0), 30 (100), 0 (0) | 0.639 |
Table 3 compares the characteristics of the study population between the groups according to their vitamin D concentration. The Kruskal-Wallis test was used for comparison. In the anemic group, 28 subjects were found to be with vitamin D deficiency with two participants having vitamin D insufficiency. In the control group, the distribution was 19 subjects with vitamin D deficiency, nine with vitamin D insufficiency, and two with vitamin D sufficiency. There was no significance between most of the parameters according to vitamin D levels. But serum ferritin showed a significant difference (p=0.001) between the three subgroups based on vitamin D levels in the control group. Among the cases, serum ferritin showed a significant difference (p=0.007) between the vitamin D subgroups.
| Parameters | Fibroid subjects without anemia, mean ± SD | Fibroid subjects with anemia, mean ± SD | |||||
| Vitamin D deficiency (<20 ng/ml) | Vitamin D insufficiency (20-30 ng/ml) | Vitamin D sufficiency (>30 ng/ml) | P-value | Vitamin D deficiency (<20 ng/ml) | Vitamin D insufficiency (20-30 ng/ml) | P-value | |
| Age, years | 41.6 ± 6.7 | 40.0 ± 8.2 | 42.5 ± 2.1 | 0.992 | 41.9 ± 6.3 | 44.0 ± 0.7 | 0.737 |
| BMI, kg/m2 | 20.1 ± 3.6 | 20.4 ± 4.8 | 22.0 ± 4.4 | 0.823 | 23.1 ± 3.7 | 23.7 ± 3.1 | 0.868 |
| SBP, mmHg | 113.0 ± 9.8 | 117.2 ± 10.3 | 116.0 ± 2.8 | 0.548 | 114.9 ± 9.1 | 115.0 ± 21.2 | 0.899 |
| DBP, mmHg | 75.7 ± 8.4 | 74.8 ± 7.0 | 67.0 ± 4.2 | 0.303 | 74.5 ± 6.7 | 80.0 ± 14.1 | 0.445 |
| Hemoglobin, g/dl | 12.6 ± 0.5 | 12.9 ± 1.0 | 12.4 ± 0.1 | 0.702 | 9.7 ± 1.5 | 9.0 ± 1.3 | 0.339 |
| MCV, fl/cell | 85.3 ± 6.1 | 88.3 ± 3.9 | 84.9 ± 1.8 | 0.221 | 74.5 ± 7.2 | 72.5 ± 13.3 | 0.739 |
| MCH, pg/cell | 27.6 ± 1.9 | 28.6 ± 1.7 | 27.7 ± 0.9 | 0.282 | 22.6 ± 3.0 | 21.3 ± 5.6 | 0.678 |
| MCHC, g/dl | 31.6 ± 1.0 | 32.2 ± 1.4 | 32.4 ± 1.5 | 0.541 | 30.1 ± 1.4 | 29.2 ± 2.4 | 0.739 |
| RBC, million/mm3 | 4.5 ± 0.5 | 4.3 ± 1.0 | 3.5 ± 0.4 | 0.131 | 4.4 ± 0.6 | 4.3 ± 0.5 | 0.934 |
| WBC, thousand cells/mm3 | 7.5 ± 1.8 | 9.2 ± 4.3 | 7.5 ± 0.6 | 0.823 | 8.3 ± 3.3 | 7.6 ± 1.6 | 0.739 |
| Platelets, lakhs/mm3 | 2.7 ± 0.7 | 3.1 ± 1.2 | 2.4 ± 0.2 | 0.503 | 3.3 ± 0.9 | 3.6 ± 0.7 | 0.533 |
| PCV, % | 38.2 ± 3.1 | 35.5 ± 7.4 | 30.1 ± 4.3 | 0.079 | 32.3 ± 4.5 | 30.6 ± 2.1 | 0.360 |
| RDW, % | 16.7 ± 3.8 | 17.6 ± 6.2 | 20.6 ± 8.4 | 0.664 | 17.8 ± 3.5 | 22.8 ± 12.2 | 1.000 |
| Urea, mg/dl | 17.3 ± 5.2 | 15.6 ± 2.7 | 20.5 ± 5.0 | 0.344 | 17.3 ± 5.1 | 20.0 ± 5.7 | 0.558 |
| Creatinine, mg/dl | 0.7 ± 0.1 | 0.7 ± 0.1 | 0.7 ± 0.1 | 0.344 | 0.7 ± 0.1 | 0.7 ± 0.1 | 0.965 |
| Ferritin, ng/ml | 40.0 ± 19.0 | 107.2 ± 25.2 | 126.3 ± 28.6 | 0.001* | 10.6 ± 8.6 | 28.5 ± 3.3 | 0.007* |
Table 4 compares the distribution of fibroid subjects with iron deficiency anemia and those with iron deficiency state based on their vitamin D levels; 28 (93.3%) subjects were found to have vitamin D deficiency, and two (6.7%) had vitamin D insufficiency in the iron deficiency anemia group. Five subjects in the study were found to have an iron deficiency state and all of them had vitamin D deficiency.
| Vitamin D levels | Fibroid subjects with iron deficiency anemia, n (%) | Fibroid subjects with iron deficiency, n (%) |
| Vitamin D deficiency | 28 (93.3) | 5 (100) |
| Vitamin D insufficiency | 2 (6.7) | 0 |
The odds ratio with 95% CI between the serum vitamin D groups (vitamin D deficiency and vitamin D insufficiency) and serum ferritin groups (low and normal ferritin levels) is shown in Table 5. The odds ratio was found to be 9.6 (95% CI: 1.1-80.9, p=0.019). This indicates that low ferritin levels are associated with vitamin D deficiency in fibroid subjects.
| Vitamin D levels | Ferritin of <12 ng/ml | Ferritin of >12 ng/ml | Odds ratio |
| Vitamin D deficiency | 23 | 24 | 9.6 (95% CI: 1.1–80.9, p=0.019) |
| Vitamin D insufficiency | 3 | 10 |
Figure 1 shows the Pearson correlation (r) between the serum ferritin levels and serum vitamin D levels among the study groups. A strong positive correlation of (r)=0.616 (p<0.001) was obtained.
Discussion
Uterine fibroids (submucosal, intramural, and subserosal fibroids) have different effects; submucosal and intramural types are presumed to cause heavy menstrual bleeding leading to anemia [13]. Factors like estrogen and progesterone, black ethnicity, and obesity are well-known risk factors for fibroids. Reproductive factors such as nulliparity, early menarche, and the use of oral contraceptives before the age of 16 years also contribute to its causation [14]. Hypovitaminosis D is believed to be a major risk factor for the development of uterine fibroids.
Recently, vitamin D has been found to have a protective effect, and both the initiation and growth of uterine fibroid might be inhibited with vitamin D supplementation [15]. Serum ferritin indicates the total body iron storage, and it represents iron status. Ferritin is decreased in subjects with iron deficiency anemia but may be increased in subjects with anemia of chronic disease and inflammation [16]. In the present study, most of the cases had microcytic hypochromic anemia; low levels of serum ferritin could be due to iron deficiency resulting from an inadequate intake of dietary iron or a negative iron balance. Katsumata et al. [17], in a rat model, have reported that iron deficiency decreased the levels of 1,25-dihydroxycholecalciferol and osteocalcin concentrations, suggesting that hydroxylation of vitamin D is dependent on iron, and hence iron-deficient rats had lower concentrations of the active form of vitamin D. In the present study, ferritin level and Hb level were the most significant factors affecting vitamin D levels. This result is consistent with previous studies [18,19]. Exposure to sunlight was more or less adequate in both the study groups, further suggesting the interrelationship of ferritin and vitamin D levels.
In terms of anemia, some studies have reported that vitamin D is positively associated with ferritin levels [20,21]. In the present study, vitamin D levels were reduced in patients with uterine fibroid and it was statistically significant in fibroid cases with anemia. Low serum vitamin D levels in fibroid cases could be due to the fact that vitamin D reduces the effect of transforming growth factor β3 (TGFβ3)-mediated expression of collagen type-1, and the expression and activity of metalloproteinase (MMP-2, MMP-9) that degrades the extracellular matrix [22]. Earlier studies have also reported the role of vitamin D in regulating the cellular signaling pathways associated with cell growth and proliferation, i.e., PCNA, CDK1, CDK2, CDK4, apoptosis, i.e., BCL2, BAD, caspase 3 as well as steroid hormone receptors. We found significantly low levels of vitamin D in fibroid cases with anemia. Serum ferritin levels are regulated by hepcidin, which plays a role in reducing iron absorption from the intestine. Vitamin D regulates the hepcidin-ferroportin axis in macrophages and the increase of vitamin D is known to reduce systemic hepcidin levels that ameliorate anemia [23]. Globally, various studies have been conducted to analyze the association between vitamin D and ferritin. Seong et al. [24] and Andıran et al. [25] reported that serum 25(OH)D was positively correlated with serum ferritin levels in patients in Korea and the US, respectively. However, Monlezun et al. [26] and de Castro et al. [27] reported that serum 25(OH)D was not associated with serum ferritin levels in adults from the US and Portugal, respectively. These inconsistent results may be due to the different populations, ethnic groups/countries, and the differences among the subjects of the studies (e.g., gender, absence or presence of diseases).
A strong positive correlation between serum ferritin and vitamin D levels was observed in the present study, which is in accordance with earlier findings. The odds ratios for iron deficiency and iron-deficiency anemia in subjects with vitamin D deficiency [25(OH)D of <15 ng/ml] were 1.86 (95% CI: 1.07-3.22) and 2.59 (95% CI: 1.11-6.07) in healthy Korean women as reported by Lee et al. [28]. In addition, Suh et al. [29] reported that 25(OH)D levels were lower in Korean women with iron deficiency anemia than in those without iron deficiency anemia (p<0.001). In our study, the finding of an odds ratio of 9.6 (1.1-80.9, p=0.019) with a 95% CI suggested that low ferritin levels are associated with vitamin D deficiency in fibroid uterus subjects. As reported, female gender, winter season, lack of sunlight exposure, residence in high latitudes, ethnicity (dark skin), clothing (clothing with low exposure), obesity, low socioeconomic status, and malnutrition are the factors affecting vitamin D levels. The present study found serum ferritin levels significantly affecting serum vitamin D levels in fibroid uterus cases with anemia.
Conclusions
Fibroid uterus cases with microcytic hypochromic anemia were found more prone to have vitamin D deficiency in the population of the Eastern Zone of India as compared to fibroid uterus women presenting without anemia. Serum ferritin and Hb levels were the important factors affecting serum vitamin D values, as exposure to sunlight was more or less adequate in both the study groups.
A strong positive correlation was observed between serum ferritin and vitamin D levels, suggesting that fibroid uterus cases with microcytic hypochromic anemia should also be evaluated for vitamin D deficiency, as timely corrective measures would improve the treatment outcomes in women with fibroid uterus.
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Original article
peer-reviewed
The Association Between Ferritin and Vitamin D Levels in Premenopausal Fibroid Uterus Cases With Anemia
Author Information
Pavuluri Swetha
Biochemistry, All India Institute of Medical Sciences, Bhubaneswar, IND
Shyam Krishnan R
Biochemistry, All India Institute of Medical Sciences, Bhubaneswar, IND
Saurav Nayak
Biochemistry, All India Institute of Medical Sciences, Bhubaneswar, IND
Sweta Singh
Obstetrics and Gynaecology, All India Institute of Medical Sciences, Bhubaneswar, IND
Ethics Statement and Conflict of Interest Disclosures
Human subjects: Consent was obtained or waived by all participants in this study. Institute Ethical Committee, All India Institute of Medical Sciences, Bhubaneswar issued approval IEC/AIIMS BBSR/STS/2019-20/11. The research proposal was submitted to the Institute Ethical Committee, AIIMS, Bhubaneswar for full board review. The study started only after obtaining approval from the Institute Ethical Committee, All India Institute of Medical Sciences, Bhubaneswar. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.
Acknowledgements
We express our appreciation for the study participants, and hospital staff members of the Department of Obstetrics and Gynaecology, Department of Biochemistry AIIMS, Bhubaneswar for assisting in this project.
Article Information
DOI
10.7759/cureus.13392
Cite this article as:
Kumari S, Swetha P, Krishnan R S, et al. (February 17, 2021) The Association Between Ferritin and Vitamin D Levels in Premenopausal Fibroid Uterus Cases With Anemia. Cureus 13(2): e13392. doi:10.7759/cureus.13392
Publication history
Peer review began: January 25, 2021
Peer review concluded: February 09, 2021
Published: February 17, 2021
Copyright
© Copyright 2021
Kumari et al. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 4.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
License
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Original article
peer-reviewed
The Association Between Ferritin and Vitamin D Levels in Premenopausal Fibroid Uterus Cases With Anemia
Figures etc.
| Parameters | Fibroid subjects without anemia, median (IQR) | Fibroid subjects with anemia, median (IQR) | P-value |
| Age, years | 42.5 (10.5) | 44.0 (7.5) | 0.736 |
| BMI, kg/m2 | 20.3 (4.7) | 22.7 (3.6) | 0.008* |
| SBP, mmHg | 110.5 (10) | 113.0 (10) | 0.804 |
| DBP, mmHg | 76.0 (10) | 73.0 (10) | 1.000 |
| Hemoglobin, g/dl | 12.5 (0.8) | 9.8 (2.0) | <0.001* |
| MCV, fl/cell | 86.5 (6.1) | 75.0 (10) | <0.001* |
| MCH, pg/cell | 28.2 (1.9) | 22.5 (5.2) | <0.001* |
| MCHC, g/dl | 31.7 (1.6) | 30.2 (1.5) | <0.001* |
| RBC, million/mm3 | 4.5 (0.9) | 4.4 (1.1) | 0.717 |
| WBC, thousand cells/mm3 | 7.1 (2.7) | 7.6 (2.3) | 0.762 |
| Platelets, lakhs/mm3 | 2.8 (1.0) | 3.3 (1.4) | 0.070 |
| PCV, % | 38.1 (7.1) | 32.3 (6.3) | <0.001* |
| RDW, % | 15.2 (5.8) | 17.2 (3.0) | 0.037* |
| Urea, mg/dl | 16.5 (5.0) | 18.0 (4.0) | 0.427 |
| Creatinine, mg/dl | 0.7 (0.2) | 0.7 (0.2) | 0.694 |
| Ferritin, ng/ml | 47.1 (59.0) | 8.0 (4.1) | <0.001* |
| Vitamin D (ng/ml) | 18.4 (7.9) | 5.0 (4.8) | <0.001* |
| Parameters | Fibroid subjects without anemia, n (%) | Fibroid subjects with anemia, n (%) | P-value | |
| Associated type 2 DM | 3 (10) | 3 (10) | 1.000 | |
| Associated hypertension | 0 (0) | 3 (10) | 0.237 | |
| Associated thyroid disorder | 6 (20) | 4 (13.3) | 0.551 | |
| Number of fibroids | 1 | 23 (76.7) | 17 (56.7) | 0.104 |
| 2 | 3 (10) | 1 (0.3) | ||
| 3 | 0 (0) | 1 (0.3) | ||
| Multiple | 4 (13.3) | 11 (36.7) | ||
| Type of fibroid | Submucosal | 7 (23.3) | 7 (23.3) | 0.072 |
| Intramural | 13 (43.3) | 20 (66.7) | ||
| Subserosal | 10 (30.3) | 3 (10) | ||
| Size of fibroid | <7 cm | 17 (56.7) | 18 (60) | 0.739 |
| >7 cm | 13 (43.3) | 12 (40) | ||
| Menarche | <13 years | 6 (20) | 11 (36.7) | 0.252 |
| >13 years | 24 (80) | 19 (63.3) | ||
| Parity | Nulliparous | 8 (26.7) | 4 (13.3) | 0.290 |
| Uniparous | 5 (16.7) | 9 (30) | ||
| Multiparous | 17 (56.7) | 17 (56.7) | ||
| History of breastfeeding | Yes | 21 (70) | 26 (86.7) | 0.209 |
| No | 9 (30) | 4 (13.3) | ||
| History of miscarriage | Yes | 8 (26.7) | 6 (20) | 0.761 |
| No | 22 (73.3) | 24 (80) | ||
| History of oral contraceptive pill use | Yes | 1 (3.3) | 2 (6.7) | 1.000 |
| No | 29 (96.7) | 28 (93.3) | ||
| Peripheral smear | Microcytic hypochromic | 2 (6.7) | 21 (70) | <0.001* |
| Normocytic normochromic | 28 (93.3) | 9 (30) | ||
| Exposure to sunlight | <1 hour/day, 1 hour/day, >1 hour/day | 0 (0), 30 (100), 0 (0) | 0 (0), 30 (100), 0 (0) | 0.639 |
| Parameters | Fibroid subjects without anemia, mean ± SD | Fibroid subjects with anemia, mean ± SD | |||||
| Vitamin D deficiency (<20 ng/ml) | Vitamin D insufficiency (20-30 ng/ml) | Vitamin D sufficiency (>30 ng/ml) | P-value | Vitamin D deficiency (<20 ng/ml) | Vitamin D insufficiency (20-30 ng/ml) | P-value | |
| Age, years | 41.6 ± 6.7 | 40.0 ± 8.2 | 42.5 ± 2.1 | 0.992 | 41.9 ± 6.3 | 44.0 ± 0.7 | 0.737 |
| BMI, kg/m2 | 20.1 ± 3.6 | 20.4 ± 4.8 | 22.0 ± 4.4 | 0.823 | 23.1 ± 3.7 | 23.7 ± 3.1 | 0.868 |
| SBP, mmHg | 113.0 ± 9.8 | 117.2 ± 10.3 | 116.0 ± 2.8 | 0.548 | 114.9 ± 9.1 | 115.0 ± 21.2 | 0.899 |
| DBP, mmHg | 75.7 ± 8.4 | 74.8 ± 7.0 | 67.0 ± 4.2 | 0.303 | 74.5 ± 6.7 | 80.0 ± 14.1 | 0.445 |
| Hemoglobin, g/dl | 12.6 ± 0.5 | 12.9 ± 1.0 | 12.4 ± 0.1 | 0.702 | 9.7 ± 1.5 | 9.0 ± 1.3 | 0.339 |
| MCV, fl/cell | 85.3 ± 6.1 | 88.3 ± 3.9 | 84.9 ± 1.8 | 0.221 | 74.5 ± 7.2 | 72.5 ± 13.3 | 0.739 |
| MCH, pg/cell | 27.6 ± 1.9 | 28.6 ± 1.7 | 27.7 ± 0.9 | 0.282 | 22.6 ± 3.0 | 21.3 ± 5.6 | 0.678 |
| MCHC, g/dl | 31.6 ± 1.0 | 32.2 ± 1.4 | 32.4 ± 1.5 | 0.541 | 30.1 ± 1.4 | 29.2 ± 2.4 | 0.739 |
| RBC, million/mm3 | 4.5 ± 0.5 | 4.3 ± 1.0 | 3.5 ± 0.4 | 0.131 | 4.4 ± 0.6 | 4.3 ± 0.5 | 0.934 |
| WBC, thousand cells/mm3 | 7.5 ± 1.8 | 9.2 ± 4.3 | 7.5 ± 0.6 | 0.823 | 8.3 ± 3.3 | 7.6 ± 1.6 | 0.739 |
| Platelets, lakhs/mm3 | 2.7 ± 0.7 | 3.1 ± 1.2 | 2.4 ± 0.2 | 0.503 | 3.3 ± 0.9 | 3.6 ± 0.7 | 0.533 |
| PCV, % | 38.2 ± 3.1 | 35.5 ± 7.4 | 30.1 ± 4.3 | 0.079 | 32.3 ± 4.5 | 30.6 ± 2.1 | 0.360 |
| RDW, % | 16.7 ± 3.8 | 17.6 ± 6.2 | 20.6 ± 8.4 | 0.664 | 17.8 ± 3.5 | 22.8 ± 12.2 | 1.000 |
| Urea, mg/dl | 17.3 ± 5.2 | 15.6 ± 2.7 | 20.5 ± 5.0 | 0.344 | 17.3 ± 5.1 | 20.0 ± 5.7 | 0.558 |
| Creatinine, mg/dl | 0.7 ± 0.1 | 0.7 ± 0.1 | 0.7 ± 0.1 | 0.344 | 0.7 ± 0.1 | 0.7 ± 0.1 | 0.965 |
| Ferritin, ng/ml | 40.0 ± 19.0 | 107.2 ± 25.2 | 126.3 ± 28.6 | 0.001* | 10.6 ± 8.6 | 28.5 ± 3.3 | 0.007* |
| Vitamin D levels | Fibroid subjects with iron deficiency anemia, n (%) | Fibroid subjects with iron deficiency, n (%) |
| Vitamin D deficiency | 28 (93.3) | 5 (100) |
| Vitamin D insufficiency | 2 (6.7) | 0 |
| Vitamin D levels | Ferritin of <12 ng/ml | Ferritin of >12 ng/ml | Odds ratio |
| Vitamin D deficiency | 23 | 24 | 9.6 (95% CI: 1.1–80.9, p=0.019) |
| Vitamin D insufficiency | 3 | 10 |
High Ferritin Levels And Low Vitamin D
Source: https://www.cureus.com/articles/50227-the-association-between-ferritin-and-vitamin-d-levels-in-premenopausal-fibroid-uterus-cases-with-anemia
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