Lower MCHC than non-carriers, making this marker not suitable to detect hypoferraemia in this group [51]. Differences in the participant’s selection criteria between the Malawian study and the present one may explain the discrepancies observed in the performance of the different iron markers studied. In the aforementioned study only severely anaemic children were included (Hb,5 g/dl), which may preclude its general applicability to the majority of anaemic children who do not have severe anaemia. In the present study all children with anaemia of any degree were recruited (Hb,11 g/dl). They were children with clinical conditions that required hospital admission and for whom investigation of anaemia is recommended in other less resourcelimited settings. The physiopathology of anaemia may vary by its severity [52], and this may be reflected in different inflammatory processes and rates of CAL-120 erythropoiesis, which may have distinct effects on the iron markers evaluated. The findings of this study show that the majority (80 ) of the anaemic children were iron deficient by direct assessment of iron stores, and that sTfR and TfR-F index adjusted by CRP are the most sensitive markers with specificities of at least 50 to identify ID in this study population. However, even with these markers, 17 and 25 of children, respectively, will not be diagnosed of ID and therefore adequately treated. The fact that the children included in the study were those attending the hospital may limit the extrapolation of the findings to children in the community. However, obvious ethical reasons would not have allowed to perform bone marrow aspirations in healthy (though may be irondeficient) children; on the other hand, children attending the hospital with anaemia are likely to be those with the 
greatest need to be diagnosed and adequately treated. In summary, even the best indirect indicators of ID not only failed to detect an important proportion of iron-deficient cases, but also their assessment is not feasible in most (��)-Hexaconazole site developing settings where the majority of ID occurs. Thus, more reliable, affordable, and easy to measure iron markers are urgently needed to reduce the burden of ID anaemia in resource-poor settings where it is more frequent and severe.AcknowledgmentsWe thank the children and their parents-guardians for their participation in the study. We are also grateful to the staff of the MDH and the CISM for their work during the study.Author ContributionsConceived and designed the experiments: RA C. Moraleda MR EM PLA C. Menendez. Performed the experiments: RA C. Moraleda JLA MR LM. ?Analyzed the data: RA C. Moraleda LQ. Wrote the paper: RA C. Moraleda C. Menendez. Interpreted the data: RA C. Moraleda LQ MR ?LM EM JLA PLA C. Menendez. Revised the article critically for important ?intellectual content: RA C. Moraleda LQ MR LM EM JLA PLA C. Menendez. Read and gave final approval of the version to be published: ?RA C. Moraleda LQ MR LM EM JLA PLA C. Menendez. ?Iron Deficiency Diagnosis and Infections
Growth hormone (GH) plays a pivotal role in multiple physiological processes in mammals. It is essential for somatic growth, is a key contributor to normal tissue differentiation and repair, and is an important regulator of intermediary metabolism [1,2]. GH also has been implicated in aging and in the development of certain cancers [1,3?], implying that in the adult its activity must be limited in scope and duration to maintain physiological homeostasis. Thus, it i.Lower MCHC than non-carriers, making this marker not suitable to detect hypoferraemia in this group [51]. Differences in the participant’s selection criteria between the Malawian study and the present one may explain the discrepancies observed in the performance of the different iron markers studied. In the aforementioned study only severely anaemic children were included (Hb,5 g/dl), which may preclude its general applicability to the majority of anaemic children who do not have severe anaemia. In the present study all children with anaemia of any degree were recruited (Hb,11 g/dl). They were children with clinical conditions that required hospital admission and for whom investigation of anaemia is recommended in other less resourcelimited settings. The physiopathology of anaemia may vary 
by its severity [52], and this may be reflected in different inflammatory processes and rates of erythropoiesis, which may have distinct effects on the iron markers evaluated. The findings of this study show that the majority (80 ) of the anaemic children were iron deficient by direct assessment of iron stores, and that sTfR and TfR-F index adjusted by CRP are the most sensitive markers with specificities of at least 50 to identify ID in this study population. However, even with these markers, 17 and 25 of children, respectively, will not be diagnosed of ID and therefore adequately treated. The fact that the children included in the study were those attending the hospital may limit the extrapolation of the findings to children in the community. However, obvious ethical reasons would not have allowed to perform bone marrow aspirations in healthy (though may be irondeficient) children; on the other hand, children attending the hospital with anaemia are likely to be those with the greatest need to be diagnosed and adequately treated. In summary, even the best indirect indicators of ID not only failed to detect an important proportion of iron-deficient cases, but also their assessment is not feasible in most developing settings where the majority of ID occurs. Thus, more reliable, affordable, and easy to measure iron markers are urgently needed to reduce the burden of ID anaemia in resource-poor settings where it is more frequent and severe.AcknowledgmentsWe thank the children and their parents-guardians for their participation in the study. We are also grateful to the staff of the MDH and the CISM for their work during the study.Author ContributionsConceived and designed the experiments: RA C. Moraleda MR EM PLA C. Menendez. Performed the experiments: RA C. Moraleda JLA MR LM. ?Analyzed the data: RA C. Moraleda LQ. Wrote the paper: RA C. Moraleda C. Menendez. Interpreted the data: RA C. Moraleda LQ MR ?LM EM JLA PLA C. Menendez. Revised the article critically for important ?intellectual content: RA C. Moraleda LQ MR LM EM JLA PLA C. Menendez. Read and gave final approval of the version to be published: ?RA C. Moraleda LQ MR LM EM JLA PLA C. Menendez. ?Iron Deficiency Diagnosis and Infections
Growth hormone (GH) plays a pivotal role in multiple physiological processes in mammals. It is essential for somatic growth, is a key contributor to normal tissue differentiation and repair, and is an important regulator of intermediary metabolism [1,2]. GH also has been implicated in aging and in the development of certain cancers [1,3?], implying that in the adult its activity must be limited in scope and duration to maintain physiological homeostasis. Thus, it i.