- Research article
- Open Access
Pica associated with iron deficiency or depletion: clinical and laboratory correlates in 262 non-pregnant adult outpatients
BMC Hematology volume 10, Article number: 9 (2010)
There are many descriptions of the association of pica with iron deficiency in adults, but there are few reports in which observations available at diagnosis of iron deficiency were analyzed using multivariable techniques to identify significant predictors of pica. We sought to identify clinical and laboratory correlates of pica in adults with iron deficiency or depletion using univariable and stepwise forward logistic regression analyses.
We reviewed charts of 262 non-pregnant adult outpatients (ages ≥18 y) who required treatment with intravenous iron dextran. We tabulated their sex, age, race/ethnicity, body mass index, symptoms and causes of iron deficiency or depletion, serum iron and complete blood count measures, and other conditions at diagnosis before intravenous iron dextran was administered. We excluded patients with serum creatinine >133 μmol/L or disorders that could affect erythrocyte or iron measures. Iron deficiency was defined as both SF <45 pmol/L and TS <10%. Iron depletion was defined as serum ferritin (SF) <112 pmol/L. We performed univariable comparisons and stepwise forward logistic regression analyses to identify significant correlates of pica.
There were 230 women (184 white, 46 black; ages 19-91 y) and 32 men (31 white, 1 black; ages 24-81 y). 118 patients (45.0%) reported pica; of these, 87.3% reported ice pica (pagophagia). In univariable analyses, patients with pica had lower mean age, black race/ethnicity, and higher prevalences of cardiopulmonary and epithelial manifestations. The prevalence of iron deficiency, with or without anemia, did not differ significantly between patients with and without pica reports. Mean hemoglobin and mean corpuscular volume (MCV) were lower and mean red blood cell distribution width (RDW) and platelet count were higher in patients with pica. Thrombocytosis occurred only in women and was more prevalent in those with pica (20.4% vs. 8.3%; p = 0.0050). Mean total iron-binding capacity was higher and mean serum ferritin was lower in patients with pica. Nineteen patients developed a second episode of iron deficiency or depletion; concordance of recurrent pica (or absence of pica) was 95%. Predictors of pica in logistic regression analyses were age and MCV (negative associations; p = 0.0250 and 0.0018, respectively) and RDW and platelet count (positive associations; p = 0.0009 and 0.02215, respectively); the odds ratios of these predictors were low.
In non-pregnant adult patients with iron deficiency or depletion, lower age is a significant predictor of pica. Patients with pica have lower MCV, higher RDW, and higher platelet counts than patients without pica.
Pica is the daily compulsive eating of food or non-food items not part of one's habitual diet or preferences. Pica is a distinctive but poorly understood accompaniment of iron deficiency or depletion in some adults, although most pica items contain little or no iron. Hippocrates wrote that "a craving to eat earth" was associated with "corruption of the blood" [1, 2]. In the early 15th C, de Cervantes reported a history in which "women that by caprice eat soil, plaster, coal and other disgusting substances" . Physicians of the 19th C reported that persons with chlorosis (predominantly women) had "various forms of pica or morbid appetite, as for pickles, magnesia, cinders, &c" , or "capricious appetite" . Individual adults with pica associated with iron deficiency or depletion typically ingest only one or a few substances in a compulsive manner. Pica items are diverse, and vary according to race/ethnicity, culture, and geographic location [1, 6–10].
Many reports describe substances that patients with iron deficiency consumed in a compulsive manner, and effects of treatment of iron deficiency on pica [1, 4, 6–12]. There are few reports in which observations available at diagnosis of iron deficiency were evaluated using multivariable analyses to identify possible significant differences between persons who did and did not develop pica. In a case-control study from France, a logistic regression model demonstrated that iron deficiency and being non-European were significant independent predictors of pica . Significant race/ethnicity differences in the prevalence of pica have also been reported in other iron deficiency case series [8, 11, 13–15]. Among iron-deficient adults of the same race/ethnicity, some develop pica and others do not [8, 11, 13–15]. These observations suggest that heritable traits could contribute to pica susceptibility in adults with iron deficiency. It is generally accepted that some patients who developed pica with an initial episode of iron deficiency will develop pica during subsequent episodes of iron deficiency [13, 16, 17]. Regardless, we were unable to identify reports in which the concordance of pica or no pica with successive episodes of iron deficiency in the same series of patients was quantified. High concordance also suggests that heritable factors increase the likelihood that pica would accompany iron deficiency.
We sought to identify clinical and laboratory correlates of pica in 262 consecutive non-pregnant adult outpatients at diagnosis of iron deficiency or depletion. These patients were referred because they needed treatment with intravenous iron. In each case, we tabulated sex, age, race/ethnicity, body mass index, symptoms attributed to iron deficiency or depletion, causes of iron deficiency or depletion, serum iron and complete blood count (CBC) measures, and other medical conditions at diagnosis of iron deficiency before intravenous iron was administered. We performed univariable and multivariable analyses to identify significant positive and negative predictors of pica. We compared and contrasted our results with previous reports of pica associated with iron deficiency, and discuss abnormalities that could account for pica in iron deficiency and depletion.
The performance of this study was approved by the Institutional Review Board of Brookwood Medical Center. We performed retrospective reviews of the charts of all adult outpatients (≥18 years of age) who were treated with intravenous iron dextran in a single referral hematology and medical oncology practice during the interval 2002-2009. Cases were identified by computerized and manual searches of practice medical and billing records for International Classification of Diseases (ICD) code 280.0 (iron deficiency), ICD code 307.52 (pica), and procedure codes corresponding to administration of intravenous iron dextran. Each patient was evaluated by either JCB or LFB. Each patient was treated with intravenous iron dextran (Imferon® or INFed®; Watson Pharma, Inc., Morristown, NJ) because he/she could not tolerate oral iron supplements; his/her iron deficiency or depletion did not resolve with trials of oral iron supplementation; or he/she had anemia or other manifestation(s) too severe to manage with oral iron supplements .
We excluded patients who were pregnant; were hospitalized; had serum creatinine >133 μmol/L; had been treated with erythrocyte transfusion to alleviate anemia; had types of acquired anemia other than that due to iron deficiency or depletion; had erythrocytosis, polycythemia, or other bone marrow disorder not in remission; were receiving anti-cancer chemotherapy or radiation therapy; or had hyperferritinemia due to acute phase reaction, chronic inflammation, liver injury, malignancy, or other cause.
CBCs were performed using Cell-Dyn® 1800 or 1500 automated blood counters (Abbott Laboratories, Chicago, IL). Reference ranges for red blood cells (RBC), mean corpuscular volume (MCV), and red blood cell distribution width (RDW) are 4.20-6.30 × 1012/L, 80.0-97.0 fL, and 11.5-14.5%, respectively. Anemia was defined as hemoglobin below these lower reference limits (133 g/L, men; 117 g/L, women) . Thrombocytopenia was defined as platelet count <140 × 109/L; thrombocytosis was defined as platelet count >440 × 109/L. Serum iron measures were determined using automated clinical laboratory methods. Total iron-binding capacity (TIBC) was defined as the sum of serum iron (SI) concentration and unbound iron-binding capacity. Transferrin saturation (TS) was defined as the quotient of serum iron concentration by TIBC. Iron deficiency was defined as both serum ferritin (SF) <45 pmol/L and TS <10%. Iron depletion was defined as SF <112 pmol/L.
Definition of pica
Pica was defined as the daily compulsive eating of food or non-food items, singly or in combination, not ordinarily part of the patient's habitual diet or preferences, for more than one month, and not reasonably attributable to causes other than iron deficiency by the patient or treating physician. We tabulated pica food and non-food items in each case. Most patients were questioned specifically at the time of their initial evaluation for iron deficiency about whether they had pica. Patients whose charts had no report of pica were classified as not having pica.
Observations for tabulation
We compiled these observations at diagnosis in all eligible patients: age, sex, self-reported race/ethnicity, body mass index (BMI), and presence (or absence) of pica reports. We also recorded and categorized symptoms attributed to iron deficiency or depletion, defined as fatigue (fatigue, weakness, decreased stamina); cardiopulmonary symptoms (shortness of breath, dyspnea on exertion, palpitations, dizziness, syncope); mental manifestations (forgetfulness, slow mentation; difficulty in performing routine mental tasks); epithelial manifestations (angular, cheilosis, glossitis, stomatitis, dysphagia, esophageal web, hair or nail changes, easy bruising); and neuromuscular symptoms (restless legs syndrome (RLS) , involuntary muscle contractions, paresthesias).
We grouped causes of iron deficiency or depletion according to these categories: 1) gastrointestinal blood loss, regardless of lesion(s); 2) reproductive tract loss (menses and previous pregnancy); 3) medical losses (laboratory testing, voluntary blood donation, therapeutic phlebotomy, or surgery); 4) chronic malabsorption (gastric bypass surgery, celiac disease, gastric resection); 5) urinary tract blood loss (hematuria); 6) recurrent epistaxis; and 7) unknown cause. One or two predominant causes were recorded in each case according to interpretation of the treating physician and our chart review.
We recorded the presence or absence of some other conditions in each subject because these conditions are common among patients in our practice: cancer in remission (any malignancy other than non-melanoma skin cancer); common variable immunodeficiency (CVID); diabetes mellitus; and HFE hemochromatosis associated with C282Y homozygosity. We compiled values of hemoglobin, RBC, MCV, and RDW; lymphocyte, neutrophil, and platelet counts; and SI, TIBC, TS, and SF levels at diagnosis before intravenous iron dextran therapy was administered.
Pica and recurrent iron depletion or deficiency
In this substudy, we tabulated the presence or absence of pica detected in patients with recurrent iron deficiency or depletion more than six months after resolution of clinical and laboratory abnormalities associated with their respective initial episodes of iron deficiency or depletion.
We reviewed the charts of 267 patients; five cases were excluded because the chart did not contain all variables specified for the present analyses. Thus, the analytic dataset included observations on 262 patients. Continuous variables included age at diagnosis, BMI, CBC values, and serum iron measures. Dichotomous variables included sex, race/ethnicity (white vs. black/African American), presence or absence of pica and other symptoms or conditions attributed to iron deficiency or depletion, causes of iron deficiency or depletion, and history or no history of cancer in remission, CVID, diabetes mellitus, and hemochromatosis. Altogether, there were 32 variables (pica and 31 others). TIBC values >86.8 μmol/L were imputed as 87.0 μmol/L; SF values reported as <4.5 pmol/L were imputed as 2.2 pmol/L. We analyzed the categories anemia, iron deficiency, iron depletion, thrombocytosis, thrombocytopenia, and anemia and iron deficiency in univariable but not multivariable analyses, because each of these categories is derived from measured values. Observations analyzed on 18 persons who had recurrent iron depletion or deficiency included recurrence of pica, CBC values, and serum iron measures.
Descriptive statistics are displayed as enumerations, percentages, frequency distribution plots, or mean ± 1 standard deviation (SD). Comparisons were made using either Student's two-sided t-test or chi-square or Fisher's exact test, as appropriate. We performed stepwise forward multiple logistic regression analyses to identify independent factors that have a significant positive or negative association with pica (dependent variable). Results of the final model are expressed as beta coefficient, standard error (SE), Wald coefficient/SE, probability, and odds ratios (95% confidence interval (CI)). Data analyses were performed using GB-Stat® v 8.0 (Dynamic Microsystems, Inc., Silver Spring, MD) and Microsoft Excel 2000® (Microsoft Corp., Redmond, WA). Values of p < 0.05 are defined as significant.
General characteristics of study subjects
All patients were treated with intravenous iron dextran in the interval November 1992-March 2009. There were 230 women (184 white, 46 black) and 32 men (31 white, 1 black). The age range of women was 19-91 years; the age range of men was 24-81 years (Table 1).
There were reports of pica in 118 patients (45.0%) (Table 1), and chart documentation of no pica in 49 other cases. Thus, there were explicit reports of pica or no pica in 63.7% of all 262 cases. Among all 262 subjects, the proportion of women with pica did not differ significantly from the proportion of men with pica (47.0% vs. 31.3%, respectively; p = 0.0943). The proportion of whites with reports of pica was lower than the proportion of blacks with pica (41.1% vs. 61.7%, respectively; p = 0.0113). Among women, the proportion of whites with reports of pica was lower than the proportion of blacks with pica (42.9% vs. 63.0%, respectively; p = 0.0145).
Fatigue, cardiopulmonary symptoms, and epithelial manifestations were common among all 262 subjects (43.9%, 35.5%, and 23.7%, respectively). Gastrointestinal blood loss occurred in 42.4% and medical blood loss in 11.8% of all subjects; 36.5% of women had reproductive tract blood loss. Chronic malabsorption occurred in 29 patients (11.2%), 28 of whom (96.6%) were women. Diagnoses of CVID and hemochromatosis were observed only in white women. Thrombocytosis occurred only in women (n = 36; 15.6%) (Table 1).
Univariable comparisons of subjects with ice pica (pagophagia) and non-ice pica
Epithelial manifestations and chronic malabsorption were less prevalent in 103 patients with pagophagia than in 15 patients with non-ice pica (Table 2). Mean MCV and the prevalence of thrombocytosis were lower in patients with pagophagia than in patients with non-ice pica. Other characteristics did not differ significantly between the two patient groups (Table 2).
Univariable comparisons of subjects with and without pica
Ice was the most common pica item (87.3% of patients with pica reports) (Table 3). Mean age and the prevalence of whites were lower in patients with pica than in patients without pica. The prevalence of pica reports was greater in white women aged 19-59 years than in older women (Figure 1). Cardiopulmonary symptoms and epithelial manifestations were more common in patients who reported pica than in those who did not report pica. Reproductive blood loss was more prevalent in patients with pica reports than in those without pica reports (Table 3). All patients with pica reported that their pica resolved within three weeks (or less) after administration of their first intravenous infusion of iron dextran.
Mean hemoglobin and mean MCV values were lower and mean RDW was higher in patients with reports of pica with than in patients without reports of pica (Table 3). Mean platelet counts and prevalence of thrombocytosis were higher in patients with reports of pica. Thrombocytosis occurred only in women and was more prevalent in those with pica (Table 3). Mean TIBC was higher and mean SF was lower in patients with pica reports. The prevalence of iron deficiency, with or without anemia, did not differ significantly between patients with and without pica reports. The prevalence of cancer in remission was lower in patients with pica (Table 3).
Five white women were previously diagnosed to have hemochromatosis, homozygosity for HFE C282Y, and iron overload phenotypes. They had been treated with phlebotomy to achieve iron depletion . They subsequently developed iron deficiency and associated symptoms at ages 34-69 years, 2-11 years after achieving iron depletion as part of iron overload management. Their causes of iron deficiency were blood loss at total knee arthroplasty (n = 2); gastrointestinal bleeding from arteriovenous malformations (n = 1); surgery and laboratory blood loss associated with breast cancer treatment (n = 1); and chronic iron malabsorption due to gastric bypass surgery (n = 1). One of these five women reported having pica (Table 3).
Recurrence of pica
Nineteen patients had recurrent iron deficiency or depletion. Fifteen had pica at first diagnosis of iron deficiency or depletion (13 white women, 1 white man, 1 black woman); 14 of the fifteen (93.3%) had pica with recurrent iron deficiency or depletion. Four other patients (all white women) did not have pica at first diagnosis; none reported pica with recurrent iron deficiency or depletion. Thus, 94.7% of these patients retained the same positive or negative pica phenotype with recurrent iron deficiency or depletion that they had at first diagnosis. The proportions of patients whose pica phenotype was the same at the initial and recurrent episodes of iron deficiency or depletion did not differ significantly (14/15 vs. 4/4, respectively; p = 0.6213, Chi-square test). At recurrence of pica, eight of fifteen subjects (53.3%) had hemoglobin and SF levels that were within the corresponding reference ranges. At recurrence of pica, mean MCV was higher and mean RDW was lower than at first diagnosis of iron deficiency or depletion; other mean CBC values and serum iron measures did not differ significantly (Table 4).
Multiple logistic regression analyses
We performed stepwise forward multiple logistic regressions using pica as the dependent variable to determine the most economical model that would include only significant explanatory independent variables. We identified four significant predictors of pica among the 31 independent variables: age and MCV (negative associations) and platelet count and RDW (positive associations) (Table 5). No other variable or combination of variables added to this four-variable model achieved statistical significance. The odds ratios and 95% confidence intervals of the four independent variables associated with reports of pica are displayed in Table 5.
Pica was the most prevalent symptom we observed (45% of patients). In other studies of adults in the U.S., the prevalence of pica was 36-61% [8, 11, 13, 14]. In contrast, pica was reported in only 0.6% of 353 iron-deficient subjects in Japan . Ice craving (pagophagia) was reported by 87% of the present subjects who reported pica, consistent with the predominance of pagophagia among subjects with pica and iron deficiency in other reports from several countries [1, 8, 10, 11, 13, 14, 16, 21, 22].
In the present patients with pagophagia, prevalences of epithelial manifestations, chronic malabsorption, thrombocytosis, and mean MCV were lower than in patients with non-ice pica. It is unknown whether differences in choices of pica items are biologically related to these manifestations. The number of patients with non-ice pica was relatively low. Further, studies involving a large number of comparisons have a high likelihood of finding statistically significant associations by chance alone (Type 1 error) . Iron absorption is not significantly affected by pagophagia [24, 25], and thus pagophagia is an improbable cause of iron deficiency or depletion.
The proportions of women and men who reported pica did not differ significantly. In two other studies, the prevalence of pica was significantly greater in women than men with iron deficiency [8, 14]. In the present women, however, the proportion of whites with pica was significantly lower than that of blacks with pica. In a series of iron deficiency cases from South Africa, there was no significant difference in the prevalence of pica between whites and blacks . We observed that the prevalence of epithelial manifestations was greater in patients with pica reports. In another study, diagnoses of fibromyalgia were significantly more prevalent in iron-deficient subjects with pica than in those without pica .
Pica was not significantly associated with the cause(s) of blood loss or iron deficiency or depletion in the present study. This is consistent with previous reports of pica in adults with iron deficiency due to menorrhagia or pregnancy ; gastrointestinal blood loss ; therapeutic phlebotomy for polycythemia rubra vera ; and malabsorption of iron due to gastric bypass [28, 29]. Pica is not a predictor of the cause of gastrointestinal blood loss in persons with iron deficiency . Although infection of the stomach with Helicobacter pylori was associated with autoimmune gastritis and iron deficiency in men [8, 30], there was no significant association of pica with H. pylori infection in adults with iron deficiency .
Mean hemoglobin levels were significantly lower in the present patients with pica than in those without pica. The prevalence of anemia, iron deficiency, or iron deficiency with anemia did not differ significantly between these two groups. Patients with pica had significantly lower mean values of MCV and significantly higher mean RDW and mean platelet counts than patients without pica. Thrombocytosis was observed only in women with pica, consistent with a previous report of platelet counts in adults with iron deficiency [31, 32]. In normal control subjects, mean platelet counts are also significantly higher in women than men . In the present analyses, mean values of TIBC and SF were significantly lower in patients with pica than in patients without pica, but the magnitude of these respective differences was small.
Five white women in the present study were previously diagnosed to have hemochromatosis with homozygosity for HFE C282Y and were treated with phlebotomy to achieve iron depletion . Later, they developed iron deficiency due to causes unrelated to therapeutic phlebotomy, like some other patients diagnosed to have HFE hemochromatosis in medical care or population screening [34–37]. The proportion of patients with reports of pica who had cancer in remission was lower than the proportion of patients without pica who had cancer in remission. In 55 unselected patients with iron-deficiency anemia due to gastrointestinal blood loss evaluated by a gastroenterology referral service at a city hospital, the proportion of patients with malignancy who had pica was significantly lower than the proportion of patients without malignancy (2/9 vs. 30/46; p = 0.0217; Fisher's exact test) .
Using multiple logistic regression analyses, we identified four significant predictors of pica among 31 independent variables: age and MCV (negative associations) and platelet count and RDW (positive associations). Regardless, the odds ratios associated with these variables were relatively low. Only age represents a condition that existed before the development of iron depletion or deficiency in our series of 262 non-pregnant adults. In a French study, age and sex were not significant predictors of pica in a multiple logistic regression model of observations from 79 patients with iron deficiency, although 40% of them were pregnant women . The other "pre-existing" factors that were significant in our univariable comparisons (sex, race/ethnicity, cancer in remission, CVID, diabetes mellitus, and hemochromatosis) were not significant independent predictors of pica in multiple logistic regression analyses. These observations suggest that pica is triggered by factors that precede routine diagnostic indicators of iron depletion or deficiency such as abnormal CBC values or serum iron measures, or structural changes in the epithelial surfaces of the lips, oral cavity, and nasopharynx [38–42].
The present results confirm that pica develops in some adults with iron depletion or iron deficiency and not in others [8, 11, 13–15], although the reason(s) for this dichotomy is not reported. The concordance of recurrent pica (or absence of pica) in 19 of present patients who developed a second episode of iron deficiency or depletion was high (95%). Further, pica recurred in some of the present patients before they developed anemia or hypoferritinemia. In another study, pica was also a relatively early indicator of recurrent iron deficiency or depletion in patients who had undergone gastric bypass surgery . Other investigators have reported that the occurrence of pica is not necessarily related to the severity of iron deficiency . Thrombopoiesis may be stimulated by early iron depletion [44, 45]. Pica in the present patients resolved rapidly after administration of intravenous iron dextran, in agreement with previous reports [4, 11, 12]. A genetic predisposition to develop pica in the presence of iron deficiency or depletion could explain these observations.
Some reports including the present one suggest that certain manifestations of iron deficiency are affected by heritable traits. TMPRSS6 (OMIM *609862; chromosome 22q12-q13) encodes matripase-2 (transmembrane serine protease 6). The TMPRSS6 allele A736V (rs855791) was related to significantly lower levels of SI, TS, MCV, and hemoglobin in two genome-wide association studies of twins and general population subjects, respectively [46, 47]. TMPRSS6 A736V could explain the small but significant differences we observed in mean MCV and hemoglobin levels in patients with and without pica reports, although this is unproven. RLS also occurs as an acquired manifestation of iron deficiency [19, 48–50], and is cured by reconstitution of iron stores .
Pica ascertainment is an uncertainty in the present study. There was no ascertainment of pica based on chart review in 36.3% of the present cases; patients whose charts had no report of pica were classified as not having pica. Nonetheless, iron depletion or deficiency in all 262 patients in this study was diagnosed and managed by the same two clinicians (JCB and LFB). Accordingly, the likelihood that a distinctive symptom such as pica was not recorded in our medical records, had it occurred, is small. It was beyond the scope of the present study to attempt to contact patients without documented ascertainment of pica for further interview on this point. Uncertainties of our study also include the possibility that some patients did not report pica because they were forgetful or embarrassed . Although the present patients were not treated with oral iron supplements, the proportions of present patients with pica and other manifestations of iron deficiency or depletion are similar to those in reports from North America in which oral iron supplementation was used [8, 11, 13, 14]. Our case series included only one black man, prohibiting us from making conclusions about pica in black men. Medications such as aspirin, non-steroidal anti-inflammatory drugs, and warfarin may increase the loss of blood (and thus iron) from the gastrointestinal tract [52–57]. Other medications, including proton pump inhibitors, histamine receptor-2 antagonists, and preparations that contain calcium, may decrease iron absorption in short-term studies [58–61]. Although we did not tabulate these medications for analysis, other variables such as blood loss from different sites or chronic malabsorption were not significantly associated with increased prevalence of pica.
In non-pregnant adult patients with iron deficiency or depletion, lower age is a significant predictor of pica. Patients with pica have lower MCV, higher RDW, and higher platelet counts than patients without pica.
Parry-Jones B: Pagophagia, or compulsive ice consumption: a historical perspective. Psychol Med. 1992, 22: 561-571. 10.1017/S0033291700038022.
Andrews N: Iron deficiency and related disorders. Wintrobe's Clinical Hematology. Edited by: Greer JP, Foerster J, Rodgers GM, Paraskevos F, Glader B, Arber DA. 2009, Lippincott Williams & Wilkins: Philadelphia, 1: 810-834. 12
Larrain C: [Pica, a strange symptom unveiled even in "Don Quixote"]. Rev Med Chil. 2005, 133: 609-611.
Hall M: Chlorosis. The Cyclopaedia of Practical Medicine. Edited by: Forbes J, Tweedie A, Conolly J, Dunglison R. 1848, Philadelphia: Lea and Blanchard, 396-399.
Stevens AA: Diseases of the Blood: Chlorosis (Green Sickness; Primary Anaemia). A Manual of the Practice of Medicine: Prepared Especially for Students. 1896, Philadelphia: W.B. Saunders, 109-118. 4
Moore DF, Sears DA: Pica, iron deficiency, and the medical history. Am J Med. 1994, 97: 390-393. 10.1016/0002-9343(94)90309-3.
al Kanhal MA, Bani IA: Food habits during pregnancy among Saudi women. Int J Vitam Nutr Res. 1995, 65: 206-210.
Barton JC, Barton EH, Bertoli LF, Gothard CH, Sherrer JS: Intravenous iron dextran therapy in patients with iron deficiency and normal renal function who failed to respond to or did not tolerate oral iron supplementation. Am J Med. 2000, 109: 27-32. 10.1016/S0002-9343(00)00396-X.
Kettaneh A, Eclache V, Fain O, Sontag C, Uzan M, Carbillon L, Stirnemann J, Thomas M: Pica and food craving in patients with iron-deficiency anemia: a case-control study in France. Am J Med. 2005, 118: 185-188. 10.1016/j.amjmed.2004.07.050.
Louw VJ, du PP, Malan A, van Deventer L, van Wyk D, Joubert G: Pica and food craving in adult patients with iron deficiency in Bloemfontein, South Africa. S Afr Med J. 2007, 97: 1069-1071.
Reynolds RD, Binder HJ, Miller MB, Chang WW, Horan S: Pagophagia and iron deficiency anemia. Ann Intern Med. 1968, 69: 435-440.
Sontag C, Kettaneh A, Fain O, Eclache V, Thomas M: [Rapid regression of prolonged pagophagia after treatment of iron deficiency]. Presse Med. 2001, 30: 321-323.
Crosby WH: Pica. JAMA. 1976, 235: 2765-10.1001/jama.235.25.2765.
Rector WG: Pica: its frequency and significance in patients with iron-deficiency anemia due to chronic gastrointestinal blood loss. J Gen Intern Med. 1989, 4: 512-513. 10.1007/BF02599550.
Uchida T, Matsuno M, Ide M, Kawachi Y: [The frequency and development of tissue iron deficiency in 6 iron deficiency anemia patients with Plummer-Vinson syndrome]. Rinsho Ketsueki. 1998, 39: 1099-1102.
Coltman CA: Pagophagia and iron lack. JAMA. 1969, 207: 513-516. 10.1001/jama.207.3.513.
Kushner RF, Gleason B, Shanta-Retelny V: Reemergence of pica following gastric bypass surgery for obesity: a new presentation of an old problem. J Am Diet Assoc. 2004, 104: 1393-1397. 10.1016/j.jada.2004.06.026.
Barton JC, Leiendecker-Foster C, Reboussin DM, Adams PC, Acton RT, Eckfeldt JH: Thyroid-stimulating hormone and free thyroxine levels in persons with HFE C282Y homozygosity, a common hemochromatosis genotype: the HEIRS study. Thyroid. 2008, 18: 831-838. 10.1089/thy.2008.0091.
Ekbom K, Ulfberg J: Restless legs syndrome. J Intern Med. 2009, 266: 419-431. 10.1111/j.1365-2796.2009.02159.x.
Barton JC, McDonnell SM, Adams PC, Brissot P, Powell LW, Edwards CQ, Cook JD, Kowdley KV: Management of hemochromatosis. Hemochromatosis Management Working Group. Ann Intern Med. 1998, 129: 932-939.
Coltman CA: Pagophagia. Arch Intern Med. 1971, 128: 472-473. 10.1001/archinte.128.3.472a.
Osman YM, Wali YA, Osman OM: Craving for ice and iron-deficiency anemia: a case series from Oman. Pediatr Hematol Oncol. 2005, 22: 127-131. 10.1080/08880010590896486.
Waalen J, Beutler E: Beware of multiple comparisons: a study of symptoms associated with mutations of the HFE hemochromatosis gene. Clin Chim Acta. 2005, 361: 128-134. 10.1016/j.cccn.2005.05.017.
Parry SD, Perkins AC, Hawkey CJ: A case of pica and iron deficiency anaemia in Nottingham. Int J Clin Pract. 1998, 52: 354-355.
Asma S, Boga C, Ozdogu H, Serin E: The association of pagophagia with Helicobacter pylori infection in patients with iron-deficiency anemia. Int J Hematol. 2009, 90: 28-32. 10.1007/s12185-009-0360-z.
Pamuk GE, Pamuk ON, Set T, Harmandar O, Yesil N: An increased prevalence of fibromyalgia in iron deficiency anemia and thalassemia minor and associated factors. Clin Rheumatol. 2008, 27: 1103-1108. 10.1007/s10067-008-0871-7.
Rector WG, Fortuin NJ, Conley CL: Non-hematologic effects of chronic iron deficiency. A study of patients with polycythemia vera treated solely with venesections. Medicine (Baltimore). 1982, 61: 382-389.
Kushner RF, Shanta RV: Emergence of pica (ingestion of non-food substances) accompanying iron deficiency anemia after gastric bypass surgery. Obes Surg. 2005, 15: 1491-1495. 10.1381/096089205774859371.
Marinella MA: Nocturnal pagophagia complicating gastric bypass. Mayo Clin Proc. 2008, 83: 961-10.4065/83.8.961.
Hershko C, Ianculovich M, Souroujon M: A hematologist's view of unexplained iron deficiency anemia in males: impact of Helicobacter pylori eradication. Blood Cells Mol Dis. 2007, 38: 45-53. 10.1016/j.bcmd.2006.09.006.
Kadikoylu G, Yavasoglu I, Bolaman Z, Senturk T: Platelet parameters in women with iron deficiency anemia. J Natl Med Assoc. 2006, 98: 398-402.
Kuku I, Kaya E, Yologlu S, Gokdeniz R, Baydin A: Platelet counts in adults with iron deficiency anemia. Platelets. 2009, 1-5.
Bain BJ: Ethnic and sex differences in the total and differential white cell count and platelet count. J Clin Pathol. 1996, 49: 664-666. 10.1136/jcp.49.8.664.
Barton JC, Bottomley SS: Iron deficiency due to excessive therapeutic phlebotomy in hemochromatosis. Am J Hematol. 2000, 65: 223-226. 10.1002/1096-8652(200011)65:3<223::AID-AJH8>3.0.CO;2-9.
Barton JC: Hemochromatosis, HFE C282Y homozygosity, and bariatric surgery: report of three cases. Obes Surg. 2004, 14: 1409-1414. 10.1381/0960892042583798.
Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, et al: Hemochromatosis and iron-overload screening in a racially diverse population. N Engl J Med. 2005, 352: 1769-1778. 10.1056/NEJMoa041534.
Barton JC, Acton RT, Dawkins FW, Adams PC, Lovato L, Leiendecker-Foster C, McLaren CE, Reboussin DM, Speechley MR, Gordeuk VR, et al: Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in whites and blacks in the Hemochromatosis and Iron Overload Screening Study. Genet Test. 2005, 9: 231-241. 10.1089/gte.2005.9.231.
Jacobs A: Iron deficiency and the oral mucous membrane. Br J Dermatol. 1969, 81: 861-862. 10.1111/j.1365-2133.1969.tb15958.x.
Rennie JS, MacDonald DG, Dagg JH: Quantitative analysis of human buccal epithelium in iron deficiency anaemia. J Oral Pathol. 1982, 11: 39-46. 10.1111/j.1600-0714.1982.tb00141.x.
Ranasinghe AW, Johnson NW, Scragg MA: Iron deficiency depresses cell proliferation in hamster cheek pouch epithelium. Cell Tissue Kinet. 1987, 20: 403-412.
Ranasinghe AW, Johnson NW, Scragg MA, Williams RA: Iron deficiency reduces cytochrome concentrations of mitochondria isolated from hamster cheek pouch epithelium. J Oral Pathol Med. 1989, 18: 582-585. 10.1111/j.1600-0714.1989.tb01557.x.
Sato S: Iron deficiency: structural and microchemical changes in hair, nails, and skin. Semin Dermatol. 1991, 10: 313-319.
Munoz JA, Marcos J, Risueno CE, de Cos C, Lopez R, Capote FJ, Martin MV, Gil JL: [Iron deficiency and pica]. Sangre (Barc). 1998, 43: 31-34.
Choi SI, Simone JV: Platelet production in experimental iron deficiency anemia. Blood. 1973, 42: 219-228.
Choi SI, Simone JV, Jackson CW: Megakaryocytopoiesis in experimental iron deficiency anemia. Blood. 1974, 43: 111-120.
Benyamin B, Ferreira MA, Willemsen G, Gordon S, Middelberg RP, McEvoy BP, Hottenga JJ, Henders AK, Campbell MJ, Wallace L, et al: Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nat Genet. 2009, 41: 1173-1175. 10.1038/ng.456.
Chambers JC, Zhang W, Li Y, Sehmi J, Wass MN, Zabaneh D, Hoggart C, Bayele H, McCarthy MI, Peltonen L, et al: Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels. Nat Genet. 2009, 41: 1170-1172. 10.1038/ng.462.
Mizuno S, Mihara T, Miyaoka T, Inagaki T, Horiguchi J: CSF iron, ferritin and transferrin levels in restless legs syndrome. J Sleep Res. 2005, 14: 43-47. 10.1111/j.1365-2869.2004.00403.x.
Godau J, Klose U, Di Santo A, Schweitzer K, Berg D: Multiregional brain iron deficiency in restless legs syndrome. Mov Disord. 2008, 23: 1184-1187. 10.1002/mds.22070.
Silber MH, Richardson JW: Multiple blood donations associated with iron deficiency in patients with restless legs syndrome. Mayo Clin Proc. 2003, 78: 52-54. 10.4065/78.1.52.
Gorder V, Kuntz S, Khosla S: Treatment of restless legs syndrome with iron infusion therapy. JAAPA. 2009, 22: 29-32.
Savon JJ, Allen ML, DiMarino AJ, Hermann GA, Krum RP: Gastrointestinal blood loss with low dose (325 mg) plain and enteric-coated aspirin administration. Am J Gastroenterol. 1995, 90: 581-585.
Fleming DJ, Jacques PF, Massaro JM, D'Agostino RB, Wilson PW, Wood RJ: Aspirin intake and the use of serum ferritin as a measure of iron status. Am J Clin Nutr. 2001, 74: 219-226.
Moore RA, Derry S, McQuay HJ: Faecal blood loss with aspirin, nonsteroidal anti-inflammatory drugs and cyclo-oxygenase-2 selective inhibitors: systematic review of randomized trials using autologous chromium-labelled erythrocytes. Arthritis Res Ther. 2008, 10: R7-10.1186/ar2355.
Blackshear JL, Baker VS, Holland A, Litin SC, Ahlquist DA, Hart RG, Ellefson R, Koehler J: Fecal hemoglobin excretion in elderly patients with atrial fibrillation: combined aspirin and low-dose warfarin vs conventional warfarin therapy. Arch Intern Med. 1996, 156: 658-660. 10.1001/archinte.156.6.658.
Greenberg PD, Cello JP, Rockey DC: Asymptomatic chronic gastrointestinal blood loss in patients taking aspirin or warfarin for cardiovascular disease. Am J Med. 1996, 100: 598-604. 10.1016/S0002-9343(96)00009-5.
Taha AS, Angerson WJ, Knill-Jones RP, Blatchford O: Upper gastrointestinal mucosal abnormalities and blood loss complicating low-dose aspirin and antithrombotic therapy. Aliment Pharmacol Ther. 2006, 23: 489-495. 10.1111/j.1365-2036.2006.02784.x.
Golubov J, Flanagan P, Adams P: Inhibition of iron absorption by omeprazole in rat model. Dig Dis Sci. 1991, 36: 405-408. 10.1007/BF01298866.
Hutchinson C, Geissler CA, Powell JJ, Bomford A: Proton pump inhibitors suppress absorption of dietary non-haem iron in hereditary haemochromatosis. Gut. 2007, 56: 1291-1295. 10.1136/gut.2006.108613.
Aymard JP, Aymard B, Netter P, Bannwarth B, Trechot P, Streiff F: Haematological adverse effects of histamine H2-receptor antagonists. Med Toxicol Adverse Drug Exp. 1988, 3: 430-448.
Barton JC, Conrad ME, Parmley RT: Calcium inhibition of inorganic iron absorption in rats. Gastroenterology. 1983, 84: 90-101.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2326/10/9/prepub
This work was supported in part by Southern Iron Disorders Center and Brookwood Biomedical.
The authors declare that they have no competing interests.
All authors reviewed and edited the manuscript, and all agreed with the form and content of the final manuscript. JCB (first author) designed the study, reviewed patient charts, performed statistical analyses, and drafted the manuscript. JCB (second author) reviewed patient charts, tabulated patient data, and performed statistical analyses. LFB contributed to the study design and reviewed patient charts.
James C Barton, J Clayborn Barton and Luigi F Bertoli contributed equally to this work.
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Barton, J.C., Barton, J.C. & Bertoli, L.F. Pica associated with iron deficiency or depletion: clinical and laboratory correlates in 262 non-pregnant adult outpatients. BMC Hematol 10, 9 (2010). https://doi.org/10.1186/1471-2326-10-9
- Iron Deficiency
- Serum Ferritin
- Mean Corpuscular Volume
- Iron Depletion
- Gastrointestinal Blood Loss