Correcting the cut‐off point of hemoglobin at high altitude favors misclassification of anemia, erythrocytosis and excessive erythrocytosis

The World Health Organization (WHO) defines anemia according age, gender, and altitude based on statistical distribution considerations and by cut-off points. Anemia in pregnancy and in children aged 6–59 months is defined as hemoglobin (Hb) concentration <11 g/dL.1 Since Hb contains almost 70% of iron in the organism, WHO recommends its measurement to determining prevalence of anemia as screening for iron deficiency (ID) despite that they recognize that anemia is not a specific indication of ID.1 Moreover, WHO recommends correcting the cut-off point of hemoglobin to define anemia in high-altitude (HA) populations. The correction ranges from adding up 0.2 g/dL to the cutoff for people living at 1000 m to 4.5 g/dL for those living at ≥4500 m.1 This correction is based on the assumption that populations living at HA increase Hb as altitude increases. Under hemoglobin correction the prevalence of anemia increases as HA increases2 suggesting these inhabitants are iron deficient when they have normal iron levels. However, in Tibetans there is a threshold effect for altitude on hemoglobin concentration rather than a continuous relationship. It is only at an altitude of >3800–4000 m that the hemoglobin concentration is elevated.3 Hepcidin is a hormone produced in the liver and considered the main regulator of iron homeostasis.4 After adulthood levels have been attained, hepcidin values will change according iron requirement, which in turn will depend on the availability of iron storage. Serum hepcidin fails when iron demand is high as it would be if highlanders were iron deficient. In Ethiopians highlanders, steady state hepcidin was not lower than at low-altitude (LA) revealing that they were not iron insufficient.5 It is unknown if the same pattern is observed in other high-altitude settlings as in the Peruvian Andes. Hb > 14.5g/dL during pregnancy is a risk factor for adverse outcomes in mothers and neonates.6, 7 Excessive erythrocytosis (EE) is diagnosed when men have Hb > 21 g/dL and women >19 g/dL.8 WHO has not considered that in correcting the Hb distribution curve for altitude, the proportion of subjects with newly defined anemia increases, but the proportion of subjects with Hb > 14.5g/dL and EE reduces. To clarify these issues, we have assessed prevalence of anemia and erythrocytosis before and after hemoglobin correction; and based on iron status markers to determine if hemoglobin at HA should be corrected; and to determine clinical outcomes associated with low and high hemoglobin levels. We have studied adults, infants and children <5 years at different altitudes in Peru. These studies were approved by the Institutional Review Board at the Universidad Peruana Cayetano Heredia, Lima and by a Committee at the Universidad Nacional del Altiplano, Puno. Informed consent was obtained according to Declaration of Helsinki in the studies with adults (n = 475) from LA (150 m) and high-altitude (3280, 3800, and 4340 m) and infants from Puno (3800 m) aged 6–24 months (n = 133). In population level analysis in 17 703 children <60 months of age from eight provinces of the Arequipa region ranging from 0 to 4500 m was used a secondary analysis of data-base provided by the Regional Direction of Health, Arequipa. Data-base included age, sex, height, weight, and hemoglobin without and with correction by altitude. Serum hepcidin concentrations were determined using a Hepcidin 25 bioactive ELISA kit (DRG Instruments GmBH. Marburg, Germany). Serum ferritin levels (ng/mL) were determined using a ELISA kit (DRG International, INC., USA). Serum soluble transferrin receptor (sTfR)(mg/L) was detected using sensitive ELISA (DRG Instruments GmBH, Frauenbergstr.18, D-35039, Germany). The index sTfR/log ferritin was calculated. Body Iron Content (BIC) was calculated from sTfR and Ferritin.9 In infants 6–24 months in Puno, the prevalence of anemia was 11.3%, but it increased to 94.7% after Hb correction (P < .01). Overall, 26.3% had ID (Ferritin ≤ 12 ng/mL) and 12% IDA (Ferritin ≤ 12 ng/mL). After Hb correction, 51.9% had normal ferritin associated to anemia (Figure 1A). In children <60 months in Arequipa Region, the prevalence of anemia was 16.1%, but increased to 50% after Hb correction (P < .01), whereas prevalence of erythrocytosis reduced from 3% to 0.7% after correction (P < .01; Figure 1B). In adults, the proportion of subjects with newly defined anemia increased from 5.5% to 19.8% (P < .01) but the proportion of subjects with EE reduced from 4.8% to 0.2% (P < .01), after correction (Table 1). (A) Prevalence of infants with normal ferritin and normal hemoglobin levels; normal ferritin and anemia (P < .01 between groups; Z-score test); iron deficiency; and iron deficiency anemia (P < .01 between groups; Z-score test). Black columns: Groups diagnosed according uncorrected hemoglobin. Striped columns: Groups diagnosed according corrected hemoglobin. (B) Prevalence of anemia and erythrocytosis in adults from Lima (150 m), Huancayo (3280 m), Puno (3800 m), and Cerro de Pasco (4340 m)(Left Column), Children less than 60 months of age from the Arequipa Region (0–4500 m) (Middle Column), and infants aged 6–24 months from Puno (3800 m). P < .01 between groups without and with hemoglobin correction (Chi square test). (C) Serum ferritin levels in infants (6–24 months) of Puno, Peru (3800 m) classified according hemoglobin status. Hb is presented with and without correction for altitude. Sample size = 133 infants. P < .01 between groups without and with hemoglobin correction (Student t test). (D) Progressive loss of body iron content. Normal children <60 months and pregnant women are defined as serum ferritin >12 ng/mL and hemoglobin (Hb)>11 g/dL. Iron Deficiency (ID) was defined as serum ferritin levels <12 ng/mL and hemoglobin >11 g/dL). Iron deficiency anemia was defined as serum ferritin lower 12 ng/mL and hemoglobin <11 g/dL. Reduction in serum ferritin and hemoglobin is aggravated associated with increase in serum soluble transferrin receptor (mg/L). (E) Infants and children of Arequipa Region, Peru with normal Z-score of height to age (Percentage) according WHO guidelines (n = 16 303 infants and children). Altitude of residence varies between 0 and 4500 m. P < .01 between groups of corrected and uncorrected hemoglobin (Z-score test). Hemoglobin correction was performed according WHO recommendations.1 (F) Association between hemoglobin levels (g/dL) and prevalence of chronic malnutrition in infants and children <60 months from Arequipa Region (0–4500 m)(Quadratic regression analysis). *P < .01 between groups before and after hemoglobin correction Uncorrected Anemia (25) Corrected Anemia (93) Uncorrected normal hemoglobin (306) Corrected normal hemoglobin (364) Infants aged 6–24 months from Puno (3800 m) having normal uncorrected hemoglobin levels (Hb:11–14.5 g/dL) showed higher serum ferritin levels than those with mild anemia (Hb:10.9–10 g/dL). If Hb was corrected, serum ferritin levels were higher in the group newly diagnosed as mild anemia suggesting that infants with normal ferritin levels were included as anemic after Hb correction. The same pattern was observed in the group with moderate anemia (Hb:9.9-7.0 g/dL; Figure 1C). Serum ferritin and BIC in anemic defined without hemoglobin correction are lower than values in anemic after correction. Serum hepcidin levels were similar between LA and HA adult women (10.51 ± 1.04 and 12.71 ± 1.47 ng/mL, respectively; P > .05) and adult men (15.06 ± 1.18 and 15.28 ± 8.82 ng/mL, respectively; P > .05). Similarly, hepcidin values were similar between normal and anemic (P > .05). Chronic Mountain Sickness (CMS) score score was also increased after Hb correction as subjects with high CMS score are moved to the left of the distribution curve after Hb correction (Table 1). In summary, adjusting Hb increase the cases of anemia that otherwise have normal BIC. Iron Deficiency Anemia (IDA) is a terminal stage of Iron Deficiency (ID) (Figure 1D). Therefore, when iron store was reduced we expect cases with low ferritin but normal Hb levels (prelatent ID), however, anemia develops when after depletion of iron store, iron availability to bone marrow decrease leading to iron deficiency erythropoiesis. The best way to validate Hb correction is the clinical outcome. At HA, correction of maternal hemoglobin reduces the risks for preterm birth and stillbirth in those women newly considered anemic, suggesting that women with normal Hb were erroneously diagnosed as anemic after correction.2 The prevalence of children with normal nutrition (Z-score height-for-Age) was significantly reduced from 82% to 53% (P < .01) in the group with normal hemoglobin after correction (Figure 1E). Surprisingly, low prevalence of chronic malnutrition was in the range of mild anemia, whereas prevalence increase with moderate/severe anemia and with Hb > 14.5 g/dL (Figure 1F). Findings in highlands of Nepal confirm than Tibetan women with low Hb concentrations have better reproductive outcomes than those with high Hb.10 In Peru, women from Puno (3800 m) have lower Hb concentration and newborns with higher birth-weight than in Huancavelica (3600 m).6 In countries with populations living at high-altitude, corrected hemoglobin values are used to make care decisions. In addition, the guidelines of the Ministry of Health in Peru as well as in other countries mandate the obligatory intervention for prevention or treatment with iron supplements in pregnant women and children.11 Particularly in populations living at HA this may expose to iron overload. Recently, a systematic review provided preclinical evidence of adverse effect of high iron intake in neonates on brain-health-related outcomes in adults.12 In conclusion, the new understanding of iron regulation reveals that hemoglobin concentration alone can be very misleading in high-altitude populations. Therefore, the WHO recommendations for correcting hemoglobin for altitude lead to an over-correction in Peru. In Andean population, hemoglobin correction by altitude favors misclassification of anemia, erythrocytosis and EE. Then, it is needed to use appropriate measures to identify ID at altitude. The authors thank to Gustavo B. Rondon-Fudinaga, Regional Manager of Health and Sandrino Rojas-Pauca, Regional Coordinator of Quality Management, Arequipa for their collaboration sharing data base of the Regional Management of Health, Arequipa. The study was supported by a Grant to the Research Circle on Plants with Effects on Health through CONCYTEC/CIENCIACTIVA, Lima, Peru, and by a grant for reagents supported by Universidad Ricardo Palma. María del Rosario Hinojosa is a Master student at the Universidad Nacional del Altiplano, Puno. Alisson Zevallos-Concha is a Doctor student at the Public Health School, University of Chile. The manuscript was principally authored by G.F.G and A.Z-C and reviewed by all authors; the study was designed by G.F.G, A.Z-C, VRdeC and VT; and data collection and analysis were performed by all authors. VT Contributed data base and performed statistical analysis and interpretation. SY contributed data base from infants and children of Arequipa and participated in the discussion about data. JB and MdelRH contributed with data collection from infants of Puno and participated in the discussion about data All authors declare no competing financial interests.