Iron Deficiency Anaemia
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Evaluation of Iron Profile in Type II Diabetes Mellitus Cases
International Journal of Biotechnology and Biochemistry ISSN 0973-2691 Volume 15, Number 1 (2019) pp. 27-37 © Research India Publications http://www.ripublication.com Evaluation of Iron Profile in Type II Diabetes Mellitus Cases Dr. Sayantaann Saha*, Dr. Roopa Murgod Department of Biochemistry Vydehi Institute of Medical Sciences and Research Centre, EPIP Area, Whitefield, Bangalore 560066, India. ABSTRACT Introduction: Type 2 diabetes mellitus is the most common metabolic disorder, characterized by chronic hyperglycemia resulting from defects in insulin secretion, insulin action, or both. Iron, a transitional metal has been shown to play a major role in pathogenesis of T2DM with a bi-directional relationship where iron affects glucose metabolism, and glucose metabolism in turn impinges on several iron metabolic pathways. Aims or Objectives: To estimate and compare the parameters related to iron metabolism viz. Serum Iron (Fe), Serum Ferritin, Serum TIBC (Total Iron Binding Capacity), Serum Transferrin and Transferrin Saturation with Fasting Blood Sugar (FBS) between T2DM patients and healthy controls and correlation of FBS with the above iron parameters. Material and methods: A case control study was conducted between 41 cases of confirmed T2DM patients and 40 age & sex matched healthy controls. Iron profile parameters & FBS were estimated in both the groups and compared. Iron parameters were also correlated with FBS. * Corresponding author(Dr. Sayantaann Saha), Email id: [email protected] 28 Dr. Sayantaann Saha, Dr. Roopa Murgod Results: Serum ferritin, Serum iron & serum transferrin saturation were found to be significantly higher in patients with T2DM compared to control group (P<0.001). Serum transferrin & serum TIBC were found to be slightly lower in cases as compared to controls (P<0.001). -
Scurvy Due to Selective Diet in a Seemingly Healthy 4-Year-Old Boy Andrew Nastro, MD,A,G,H Natalie Rosenwasser, MD,A,B Steven P
Scurvy Due to Selective Diet in a Seemingly Healthy 4-Year-Old Boy Andrew Nastro, MD,a,g,h Natalie Rosenwasser, MD,a,b Steven P. Daniels, MD,c Jessie Magnani, MD,a,d Yoshimi Endo, MD,e Elisa Hampton, MD,a Nancy Pan, MD,a,b Arzu Kovanlikaya, MDf Scurvy is a rare disease in developed nations. In the field of pediatrics, it abstract primarily is seen in children with developmental and behavioral issues, fDivision of Pediatric Radiology and aDepartments of malabsorptive processes, or diseases involving dysphagia. We present the Pediatrics and cRadiology, NewYork-Presbyterian/Weill Cornell Medical Center, New York, New York; bDivision of case of an otherwise developmentally appropriate 4-year-old boy who Pediatric Rheumatology and eDepartment of Radiology, developed scurvy after gradual self-restriction of his diet. He initially Hospital for Special Surgery, New York, New York; and d presented with a limp and a rash and was subsequently found to have anemia Division of Neonatal-Perinatal Medicine, University of Michigan, Ann Arbor, Michigan gDepartment of Pediatrics, and hematuria. A serum vitamin C level was undetectable, and after review of NYU School of Medicine, New York, New York hDepartment of the MRI of his lower extremities, the clinical findings supported a diagnosis of Pediatrics, Bellevue Hospital Center, New York, New York scurvy. Although scurvy is rare in developed nations, this diagnosis should be Dr Nastro helped conceptualize the case report, considered in a patient with the clinical constellation of lower-extremity pain contributed to writing the introduction, initial presentation, hospital course, and discussion, and or arthralgias, a nonblanching rash, easy bleeding or bruising, fatigue, and developed the laboratory tables while he was anemia. -
Specialty Ferritin
Specialty Ferritin Analyte Information 1 2011-04-04 Ferritin Introduction Ferritin is an intracellular iron-binding protein that stores iron and releases it in a controlled fashion. The protein is produced by almost all living organisms, including bacteria and algae. In humans, it acts as a buffer against iron deficiency and iron overload1. Most of the iron stored in the body is bound to ferritin. Ferritin is found in almost all tissues of the body, but especially in hepatocytes in the liver, reticuloendothelial cells in the spleen, skeletal tissue, muscles and bone marrow. The amount of ferritin in the blood correlates well with total iron content in the body. Ferritin (Fig.1) has a molecular weight of 450 kDa. Fig.1: Ferritin1 2 2011-04-04 Structure Ferritin consists of an appoferritin protein shell surrounding a cavity in which relatively large amounts of iron can be stored. The central core holds up to 4500 iron ions in the form of ferric hydroxyphosphate. The appoferritin shell is composed of 24 subunits, which are either light (L) or heavy (H) ferritin chains. The relative proportion of light and heavy chains differs from tissue to tissue. L-rich ferritin is found in the spleen, liver and placenta. H- rich ferritin is found in the heart and in red blood cells. Physiological Function Ferritin is the primary protein responsible for iron storage. In the physiology of iron metabolism, ferritin plays the important role of maintaining iron in a soluble, nontoxic and biologically useful form. It isolates and stores vast quantities of iron and acts as a buffer against normal physiological variation in the iron requirements of tissues2. -
K392-100 Total Iron-Binding Capacity (TIBC) and Serum Iron Assay Kit (Colorimetric)
FOR RESEARCH USE ONLY! Total Iron-Binding Capacity (TIBC) and Serum Iron Assay Kit (Colorimetric) rev 08/19 (Catalog # K392-100; 100 assays; Store at -20°C) I. Introduction: BioVision’s TIBC and Serum Iron Assay Kit measures both Total iron-binding capacity (TIBC) and Serum iron. Those values indicate the requisite iron for transferrin saturation and Serum Iron respectively. In humans, Transferrin is a blood protein that binds and transports iron throughout the body. Iron bound to transferrin and not bound are reflected in the following: 1) Total Iron Binding Capacity, 2) Unbound Iron, 3) Transferrin Saturation Bound Iron, and 4) Free Iron. Those measurements can be used for to detect and monito transferrin saturation and also iron-deficiency anemia and chronic inflammatory diseases. Part A: TIBC Part B: Serum Iron 1 1 2 2 3 3 4 II. Application: Determination of TIBC, Unbound Iron, Transferrin Saturation, Serum Iron III. Sample Type: Serum or plasma. Serum-off-the clot is preferable to normal serum. IV. Kit Contents: Components K392-100 Cap Code Part Number TIBC Assay Buffer 25 ml WM K392-100-1 Iron Solution 100 µl Blue K392-100-2 TIBC Detector 2 x 1.5 ml Brown K392-100-3 TIBC Developer 5 ml NM K392-100-4 Iron Standard (100 mM) 100 µl Yellow K392-100-5 V. User Supplied Reagents and Equipment: • 96-well plate clear plate with flat bottom • Microplate reader capable of absorbance reading VI. Storage Conditions and Reagent Preparation: Store kit at -20°C, protected from light. Briefly centrifuge small vials prior to opening. -
Gamma-Glutamyltransferase: a Predictive Biomarker of Cellular Antioxidant Inadequacy and Disease Risk
Hindawi Publishing Corporation Disease Markers Volume 2015, Article ID 818570, 18 pages http://dx.doi.org/10.1155/2015/818570 Review Article Gamma-Glutamyltransferase: A Predictive Biomarker of Cellular Antioxidant Inadequacy and Disease Risk Gerald Koenig1,2 and Stephanie Seneff3 1 Health-e-Iron, LLC, 2800 Waymaker Way, No. 12, Austin, TX 78746, USA 2Iron Disorders Institute, Greenville, SC 29615, USA 3Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA 02139, USA Correspondence should be addressed to Gerald Koenig; [email protected] Received 2 July 2015; Accepted 20 September 2015 Academic Editor: Ralf Lichtinghagen Copyright © 2015 G. Koenig and S. Seneff. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Gamma-glutamyltransferase (GGT) is a well-established serum marker for alcohol-related liver disease. However, GGT’s predictive utility applies well beyond liver disease: elevated GGT is linked to increased risk to a multitude of diseases and conditions, including cardiovascular disease, diabetes, metabolic syndrome (MetS), and all-cause mortality. The literature from multiple population groups worldwide consistently shows strong predictive power for GGT, even across different gender and ethnic categories. Here, we examine the relationship of GGT to other serum markers such as serum ferritin (SF) levels, and we suggest a link to exposure to environmental and endogenous toxins, resulting in oxidative and nitrosative stress. We observe a general upward trend in population levels of GGT over time, particularly in the US and Korea. Since the late 1970s, both GGT and incident MetS and its related disorders have risen in virtual lockstep. -
Iron Deficiency and Endurance Athletes By
The undersigned, appointed by the Vice President of the Graduate School, have examined the dissertation entitled: Iron Deficiency and Endurance Athletes by: Jamin Swift A candidate for the degree of Doctor of Education And hereby certify that in their opinion it is worthy of acceptance April 2018 Approved: Chair: __________________________________________________________________ (Dr. Paul Sturgis, Ed. D, Chair) __________________________________________________________________ (Dr. Doug Ebersold, Ed. D, Committee Member) __________________________________________________________________ (Dr. Lynn Hanrahan, Ed. D, Committee Member) __________________________________________________________________ (Dr. J. Michael Pragman, Ed. D, Committee Member) Iron Deficiency and Endurance Athletes by Jamin Swift A Dissertation Presented to the Faculty of the Graduate College William Woods University in Partial Fulfillment of the Requirement for the Degree Doctor of Education May 2018 3 Abstract The purpose of this study was to explore the various opinions concerning the importance of testing multiple markers of iron status while examining the current knowledge base in relation to the effects of iron depletion on endurance athletes. Contrasting beliefs exist pertaining to the differing methods for screening iron status as well as differing opinions regarding healthy ranges on those assessments. This study utilized an exploratory research approach to determine which diagnostic tests physicians deem most beneficial in determining iron deficiency in endurance -
Volume 1, Chapter 10 – Hematology
WASHINGTON STATE WIC POLICY AND PROCEDURE MANUAL VOLUME 1, CHAPTER 10 Hematology DOH 960-105 March 2014 In accordance with Federal law and Department of Agriculture USDA policy, this institution is prohibited from discriminating on the basis of race, color, national origin, sex, age, or disability. To file a complaint of discrimination, write USDA, Director, Office of Adjudication, 1400 Independence Avenue, SW, Washington, D.C. 20250-9410 or call toll free (866) 632-9992 (Voice). Individuals who are hearing impaired or have speech disabilities may contact USDA through the Federal Relay Service at (800) 877-8339; or (800) 845-6136 (Spanish). USDA is an equal opportunity provider and employer. Washington State WIC Nutrition Program does not discriminate. For persons with disabilities, this document is available on request in other formats. To submit a request, please call 1-800-841-1410 (TDD/TTY 711). DOH 960-105 March 2014 CHAPTER 10 HEMATOLOGY TABLE OF CONTENTS Section 1 - Licenses ........................................................................................................................1 The WIC Clinic as a Medical Test Site ...............................................................................1 Medical Assistants ...............................................................................................................3 Section 2 - When to Assess Clients' Iron Status ..........................................................................5 Assess Iron Status of Infants Certified from Birth through Five Months -
The Use of Mean Corpuscular Volume (MCV) to Classify the Anemia As
The Frequency of Iron Deficiency Anemia and Thalassemia Trait among Children: Experience at Prince Rashed Bin Al- Hassan Military Hospital Zuhair Nusair MD*, Abdelrazzaq Al-Wraikat MD**, Nazih Abu Al-Shiekh MD**, Sameer Kofahi MD^, Mohammad Zoubi MD^ ABSTRACT Objectives: To determine the frequency of iron deficiency anemia and thalassemia trait among children attending the Pediatric Department at Prince Rashed Bin Al-Hassan Military Hospital in the North of Jordan. Methods: This hospital based study was conducted in the year 2008 on 1,012 children aged 6 months to 14 years who attended the Pediatric Department at Prince Rashed Bin Al-Hassan Military Hospital in North of Jordan using fully automated blood count of the mean corpuscular volume, serum ferritin level and high performance liquid chromography, or genotyping. None of the subjects included in the study had been on any hematinic in the previous six months, had infection in the past one month or had a chronic disease. The diagnosis of iron deficiency anemia was defined as mean corpuscular volume ≤ mean – 1 standard deviation corrected for age, with a ferritin level < 7 ng/ml of the serum (normal reference range 7 – 140 ng/ml). The diagnosis of thalassemia trait, for subjects with normal or high serum ferritin and those whose mean corpuscular volume was non-compliant to iron therapy, was obtained by high performance liquid chromography or polymerase chain reaction, which was performed at Princess Eman Research and Laboratory Science Center. Results: The frequency of iron deficiency anemia and thalassemia trait was 13.3% and 5.8% respectively. They were equally frequent among males and females. -
Iron Deficiency and the Anemia of Chronic Disease
Thomas G. DeLoughery, MD MACP FAWM Professor of Medicine, Pathology, and Pediatrics Oregon Health Sciences University Portland, Oregon [email protected] IRON DEFICIENCY AND THE ANEMIA OF CHRONIC DISEASE SIGNIFICANCE Lack of iron and the anemia of chronic disease are the most common causes of anemia in the world. The majority of pre-menopausal women will have some element of iron deficiency. The first clue to many GI cancers and other diseases is iron loss. Finally, iron deficiency is one of the most treatable medical disorders of the elderly. IRON METABOLISM It is crucial to understand normal iron metabolism to understand iron deficiency and the anemia of chronic disease. Iron in food is largely in ferric form (Fe+++ ) which is reduced by stomach acid to the ferrous form (Fe++). In the jejunum two receptors on the mucosal cells absorb iron. The one for heme-iron (heme iron receptor) is very avid for heme-bound iron (absorbs 30-40%). The other receptor - divalent metal transporter (DMT1) - takes up inorganic iron but is less efficient (1-10%). Iron is exported from the enterocyte via ferroportin and is then delivered to the transferrin receptor (TfR) and then to plasma transferrin. Transferrin is the main transport molecule for iron. Transferrin can deliver iron to the marrow for the use in RBC production or to the liver for storage in ferritin. Transferrin binds to the TfR on the cell and iron is delivered either for use in hemoglobin synthesis or storage. Iron that is contained in hemoglobin in senescent red cells is recycled by binding to ferritin in the macrophage and is transferred to transferrin for recycling. -
Iron Deficiency Anemia: Evaluation and Management MATTHEW W
Iron Deficiency Anemia: Evaluation and Management MATTHEW W. SHORT, LTC, MC, USA, and JASON E. DOMAGALSKI, MAJ, MC, USA Madigan Healthcare System, Tacoma, Washington Iron deficiency is the most common nutritional disorder worldwide and accounts for approxi- mately one-half of anemia cases. The diagnosis of iron deficiency anemia is confirmed by the findings of low iron stores and a hemoglobin level two standard deviations below normal. Women should be screened during pregnancy, and children screened at one year of age. Supple- mental iron may be given initially, followed by further workup if the patient is not responsive to therapy. Men and postmenopausal women should not be screened, but should be evaluated with gastrointestinal endoscopy if diagnosed with iron deficiency anemia. The underlying cause should be treated, and oral iron therapy can be initiated to replenish iron stores. Paren- teral therapy may be used in patients who cannot tolerate or absorb oral preparations. (Am Fam Physician. 2013;87(2):98-104. Copyright © 2013 American Academy of Family Physicians.) ▲ Patient information: ron deficiency anemia is diminished red causes of microcytosis include chronic A handout on iron defi- blood cell production due to low iron inflammatory states, lead poisoning, thalas- ciency anemia, written by 1 the authors of this article, stores in the body. It is the most com- semia, and sideroblastic anemia. is available at http://www. mon nutritional disorder worldwide The following diagnostic approach is rec- aafp.org/afp/2013/0115/ I and accounts for approximately one-half of ommended in patients with anemia and is p98-s1.html. Access to anemia cases.1,2 Iron deficiency anemia can outlined in Figure 1.2,6-11 A serum ferritin level the handout is free and unrestricted. -
The Relationship Between Serum Vitamin D Level, Anemia, and Iron Deficiency in Preschool Children
HAYDARPAŞA NUMUNE MEDICAL JOURNAL DOI: 10.14744/hnhj.2019.48278 Haydarpasa Numune Med J 2019;59(3):220–223 ORIGINAL ARTICLE hnhtipdergisi.com The Relationship Between Serum Vitamin D Level, Anemia, and Iron Deficiency in Preschool Children Ömer Kartal, Orhan Gürsel Department of Pediatric Hematology and Oncology, Gulhane Training and Research Hospital, Ankara, Turkey Abstract Introduction: Vitamin D deficiency and iron deficiency are the most common nutritional pandemic problems worldwide at all levels of society. In some studies, vitamin D has been shown to have an effect on erythropoiesis. The objective of this study was to investigate the relationship between serum vitamin D level, hemogram parameters, and serum iron level in preschool children. Methods: The study group comprised 108 children aged between 2 and 5 years who visited a single pediatric hematology polyclinic between August 2014 and August 2017and whose serum vitamin D level and iron parameters were evaluated. The patients were divided into 3 groups according to the hemoglobin value, serum ferritin level, and transferrin saturation index calculation: iron deficiency, iron deficiency anemia, and a control group. Vitamin D deficiency, insufficiency, and normal cate- gories were also used based on assessment of the serum vitamin D level. Results: There were 41 children in the iron deficiency group, 32 classified as iron deficiency anemia, and 35 age- and sex- mated controls. The vitamin D level was statistically significant between the groups (p<0.05). Discussion and Conclusion: According to our findings, vitamin D deficiency and insufficiency were prevalent, especially in children with iron deficiency anemia. It is recommended that the serum vitamin D level of children with iron deficiency ane- mia should be checked and vitamin D-fortified food consumption should be increased. -
Mean Corpuscular Hemoglobin (MCH) As a Predictor of Iron Deficiency in Infants
Pediatr. Res. 16: 168-170 (1982) Diagnosis of Iron Deficiency: Mean Corpuscular Hemoglobin (MCH) as a Predictor of Iron Deficiency in Infants G. J. KNIGHT, H. DE V. HEESE,"'' W. S. DEMPSTER, AND G. KIRSTEN Department of Paediatrics and Child Health, Institute of Child Health, University of Cape Town and Red Cross War Memorial Children's Hospital, Rondebosch 7700, Cape Town, Republic of South Africa Summary an infant population. Their interpretation during childhood is further compounded by factors such as age and periods of rapid Hematologic variables were measured in 240 apparently healthy growth. To overcome some of these difficulties, various combi- infants ranging from 1-12 months of age attending a well baby nations of tests have been suggested to assist in the diagnosis of clinic. There were 20 infants for each month of age. Hematologic mild iron deficiency (3, 7, 10, 12, 13, 14). In our hands they have parameters were measured in each infant by Coulter Counter not proved satisfactory and their cost prohibitive in a developing Model S. Serum iron, total iron binding capacity, free erythrocyte country. protoporphyrin (FEP) and serum ferritin levels were measured in A statistical exercise was embarked upon to establish the most most infants. Their weights together with their serum iron, total useful single hematologic parameter for the assessment of the iron iron binding capacity, and serum ferritin were judged to be inde- status of an infant. It formed part of a study to determine the pendent variables of iron status, whereas the hematologic variables prevalence of iron deficiency anemia during infancy in a com- were considered to be response variables indicative of iron status.