Hemorrhage-adjusted iron requirements, hematinics and hepcidin define hereditary hemorrhagic telangiectasia as a model of hemorrhagic iron deficiency

Helen Finnamore, James Le Couteur, Mary Hickson, Mark Busbridge, Kevin Whelan, Claire L Shovlin, Helen Finnamore, James Le Couteur, Mary Hickson, Mark Busbridge, Kevin Whelan, Claire L Shovlin

Abstract

Background: Iron deficiency anemia remains a major global health problem. Higher iron demands provide the potential for a targeted preventative approach before anemia develops. The primary study objective was to develop and validate a metric that stratifies recommended dietary iron intake to compensate for patient-specific non-menstrual hemorrhagic losses. The secondary objective was to examine whether iron deficiency can be attributed to under-replacement of epistaxis (nosebleed) hemorrhagic iron losses in hereditary hemorrhagic telangiectasia (HHT).

Methodology/principal findings: The hemorrhage adjusted iron requirement (HAIR) sums the recommended dietary allowance, and iron required to replace additional quantified hemorrhagic losses, based on the pre-menopausal increment to compensate for menstrual losses (formula provided). In a study population of 50 HHT patients completing concurrent dietary and nosebleed questionnaires, 43/50 (86%) met their recommended dietary allowance, but only 10/50 (20%) met their HAIR. Higher HAIR was a powerful predictor of lower hemoglobin (p = 0.009), lower mean corpuscular hemoglobin content (p<0.001), lower log-transformed serum iron (p = 0.009), and higher log-transformed red cell distribution width (p<0.001). There was no evidence of generalised abnormalities in iron handling Ferritin and ferritin(2) explained 60% of the hepcidin variance (p<0.001), and the mean hepcidinferritin ratio was similar to reported controls. Iron supplement use increased the proportion of individuals meeting their HAIR, and blunted associations between HAIR and hematinic indices. Once adjusted for supplement use however, reciprocal relationships between HAIR and hemoglobin/serum iron persisted. Of 568 individuals using iron tablets, most reported problems completing the course. For patients with hereditary hemorrhagic telangiectasia, persistent anemia was reported three-times more frequently if iron tablets caused diarrhea or needed to be stopped.

Conclusions/significance: HAIR values, providing an indication of individuals' iron requirements, may be a useful tool in prevention, assessment and management of iron deficiency. Iron deficiency in HHT can be explained by under-replacement of nosebleed hemorrhagic iron losses.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1. Actual and recommended dietary iron…
Figure 1. Actual and recommended dietary iron intakes for the 50 study participants.
A) Current recommendations using US recommended dietary allowance (RDA [2]) values for iron (blue dropped line circles, at 8 or 18 mg/day): the left hand five datasets, with higher RDA values, represent the five premenopausal women, the remaining 45 datasets with lower RDA values represent males and post menopausal females. Red columns indicate each individual’s iron intake per day from their personalised food frequency questionnaire (FFQ, intake of 130 food items presented in Table S1). Note that the RDA was not met by any of the pre-menopausal females. B) HAIR recommendations: The same intake data as in A) are now illustrated on a natural logarithmic scale to allow presentation of each individual’s personalised HAIR value, calculated according to their personalised iron losses, and US based recommended dietary allowance (RDA) for iron, presented in Table 1. Note that a log(HAIR) of 3 corresponds to a HAIR of 20 mg/day (approximate needs of a male blood donor); a log(HAIR) of 4 to a HAIR of 55 mg/day (approximate needs over 3 months to replace a 3–4 g/dl drop in hemoglobin), and a log(HAIR) of 5 to a HAIR of 148 mg/day. Generally short (0.5–2.5 min) nosebleeds less than once per month resulted in log(HAIR) of approximately 2; several nosebleeds per week of 5 minutes or more in a log(HAIR) of ∼3; daily 10 min nosebleeds a log(HAIR) of ∼4, and several nosebleeds per day, each lasting 2.5–10 minutes, in a log(HAIR) of 5.
Figure 2. Raw data on nosebleed frequency…
Figure 2. Raw data on nosebleed frequency and duration.
Typical number of nosebleeds per month (blue symbols/lines, data from ESS question 1), and typical duration of nosebleeds per month (red symbols/lines, data from ESS question 2) reported by the 50 study participants, ordered by increasing value of HAIR. Nosebleeds reported as “typically gushing or pouring” were significantly longer than nosebleeds reported as “typically not gushing or pouring” (mean [standard deviation] 8.9 [6.4], versus 4.5 [4.9] minutes, Mann Whitney p = 0.0038).
Figure 3. Details of the nosebleeds reported…
Figure 3. Details of the nosebleeds reported by the online survey respondents.
A) Reported volume (mls) of individual nosebleeds, converted where appropriate from original units of measurement to mls as described in the methods. B) Reported duration (minutes) of individual nosebleeds. Corroborating evidence for specified major bleeds was provided by 16 individuals, and included acute hemodynamic consequences (faints, collapses, n = 5); hematocrit/hemoglobin falls (n = 4 including 3.2 g/dl hemoglobin fall in 8 hours; 8 units of hematocrit over 3 days); and unspecified acute transfusions or hospital admission (n = 8). There was no corroboratory evidence for the two indicated outliers (red crosses) whose values were excluded from calculations for the median, 20th and 5th percentile values used in nosebleed rate conversions.
Figure 4. Iron intakes from diet and…
Figure 4. Iron intakes from diet and iron supplements.
The nine individuals using ferrous sulphate, ferrous gluconate, ferrous fumarate or other iron supplements, are illustrated with pairwise comparisons of their dietary iron intake from the FFQ (left red bar) and dietary FFQ intake plus their supplement iron intake (right red bar) in addition to each individual’s log(RDA) and personalised log(HAIR), which were calculated according to their personalised iron losses and RDA for iron. As in Figure 1, note that generally short (0.5–2.5 min) nosebleeds less than once per month resulted in log(HAIR) of approximately 2; several nosebleeds per week of 5 minutes or more in a log(HAIR) of ∼3; daily 10 min nosebleeds a log(HAIR) of ∼4, and several nosebleeds per day, each lasting 2.5–10 minutes, in a log(HAIR) of 5. The two highest intakes were seen in individuals using ferrous sulphate 325 mg bd; the next six in users of once daily ferrous sulphate or ferrous fumarate.
Figure 5. Stratification of blood hematinic and…
Figure 5. Stratification of blood hematinic and iron indices according to HAIR values and iron supplement use.
A–E: Distributions of all participants, either by conventional recommended dietary allowance (RDA, left two box plots (mens., menses distinguishing males and post menopausal women from pre-menopausal women), or by approximate quintile (Qu) determined by HAIR (right five box plots, exact figures provided in methods). A) HAIR values (mg of iron per day). B) Serum iron (µmol/L). C) Hemoglobin (Hb, g/dL)). D) Mean corpuscular hemoglobin concentration (MCHC, g/dl). E) Red cell distribution width (RDW). F) Quadratic regression plots for the distribution of hemoglobin according to HAIR, in study participants using oral iron supplements (continuous line with 95% confidence interval indicated), and those who did not (dotted line).
Figure 6. Relationships between hepcidin and iron…
Figure 6. Relationships between hepcidin and iron indices.
A and B) Hepcidin levels according to approximate tertile groupings of A) serum iron, and B) serum ferritin. Note that the reference range for hepcidin using this radioimmunoassay is 1.1–55 ng/mL. Details of individual participants are provided in Table 4. C) and D) Best fit quadratic regression relationships (with shaded areas indicating the 95% confidence intervals) for hepcidin with C) serum iron, and D) ferritin.

References

    1. McLean E, Cogswell M, Egli I, Wojdyla D, Benoist B (2009) Worldwide prevalence of anaemia, WHO Vitamin and Mineral Nutrition Information System, 1993–2005. Public Health Nutr 12: 444–54.
    1. Center for Disease Control (2002) Iron Deficiency United States, 1999–2000. MMWR Weekly 51: 897–899. Available: . Accessed 2013 Sep 9.
    1. World Health Organization (2002) The World Health Report 2002: Reducing Risks, Promoting Healthy Life. Geneva 2002. Available: . Accessed 2013 Sep 9.
    1. Ganz T (2011) Hepcidin and iron regulation, 10 years later. Blood 117: 4425–33.
    1. Shaw STJ, Aaronson DE, Moyer DL (1972) Quantitation of menstrual blood loss-further evaluation of the alkaline hematin method. Contraception 5: 497–513.
    1. Hallberg L, Högdahl A-M, Nilsson L, Rybo G (1966) Menstrual blood loss and iron deficiency. Acta Medica Scandinavica 180: 639–50.
    1. Nelson M, Erens B, Bates B, Church S, Boshier T, editors (2007) Low income diet and nutrition survey – Food Standards Agency. London: The Stationary Office.
    1. Thane C, Bates C, Prentice A (2003) Risk factors for low iron intake and poor iron status in a national sample of British young people aged 4–18 years. Public Health Nutr 6: 485–96.
    1. Goddard AF, James MW, McIntyre AS, Scott BB (2011) British Society of Gastroenterology (2011) Guidelines for the management of iron deficiency anaemia. Gut 60: 1309–1316.
    1. United Nations Children’s Fund, United Nations University and World Health Organization (2001) Iron deficiency anaemia: assessment, prevention, and control. A guide for programme managers. WHO/NHD/01.3 Geneva.
    1. Centers for Disease Control and Prevention (1998) Recommendations to prevent and control iron deficiency in the United States. MMWR Recomm Rep 47: 1e36.
    1. Anand IS, Chandrashekhar Y, Wander GS, Chawla LS (1995) Endothelium-derived relaxing factor is important in mediating the high output state in chronic severe anemia. J Am Coll Cardiol 25: 1402–7.
    1. Smith TG, Balanos GM, Croft QP, Talbot NP, Dorrington KL, et al. (2008) The increase in pulmonary arterial pressure caused by hypoxia depends on iron status. J Physiol 586: 5999–6005.
    1. Livesey JA, Manning R, Meek JH, Jackson JE, Kulinskaya E, et al. (2012) Low serum iron levels are associated with elevated plasma levels of coagulation factor VIII and pulmonary emboli/deep venous thromboses in replicate cohorts of patients with hereditary hemorrhagic telangiectasia. Thorax 67: 328–33.
    1. Guttmacher AE, Marchuk DA, White RI (1995) Hereditary hemorrhagic telangiectasia. New Engl J Med 333: 918–924.
    1. Faughnan ME, Palda VA, Garcia-Tsao G, Geisthoff UW, McDonald J, et al. (2011) International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia. J Med Genet 48: 73–87.
    1. Shovlin CL (2010) Hereditary hemorrhagic telangiectasia: pathophysiology, diagnosis and treatment. Blood Rev 24: 203–19.
    1. Buscarini E, Leandro G, Conte D, Danesino C, Daina E, et al. (2011) Natural history and outcome of hepatic vascular malformations in a large cohort of patients with hereditary hemorrhagic telangiectasia. Dig Dis Sci 56: 2166–78.
    1. Whyte MK, Hughes JM, Jackson JE, Peters AM, Hempleman SC, et al. (1993) Cardiopulmonary response to exercise in patients with intrapulmonary vascular shunts. J Appl Physiol 75: 321–328.
    1. Androne AS, Katz SD, Lund L, LaManca J, Hudaihed A, et al. (2003) Hemodilution is common in patients with advanced heart failure. Circulation 107: 226–9.
    1. Zeidman A, Fradin Z, Blecher A, Oster HS, Avrahami Y, et al. (2004) Anemia as a risk factor for ischemic heart disease. Isr Med Assoc J 6: 16–8.
    1. Alleyne M, Horne MK, Miller JL (2008) Individualized treatment for iron-deficiency anemia in adults. Am J Med 121: 943–8.
    1. Spielmann M, Luporsi E, Ray-Coquard I, de Botton S, Azria D, et al. (2012) Diagnosis and management of anemia and iron deficiency in patients with hematological malignancies or solid tumours in France in 2009–2010: the AnemOnHe study. Eur J Cancer 48: 101–7.
    1. Goodnough LT, Maniatis A, Earnshaw P, Benoni G, Beris P, et al. (2011) Detection, evaluation, and management of preoperative anaemia in the elective orthopaedic surgical patient: NATA guidelines. Br J Anaesth 106: 13–22.
    1. Milman N (2012) Postpartum anemia II: prevention and treatment. Ann Hematol 91: 143–54.
    1. Royal Pharmaceutical Society of Great Britain and British Medical Association (2012) British National Formulary 63: BMJ Publishing Group, London.
    1. Hallberg L, Ryttinger L, Solvell L (1966) Side-effects of oral iron therapy. A double-blind study of different iron compounds in tablet form. Acta Med Scand Suppl 459: 3–10.
    1. Centers for Disease Control and Prevention (2011). Nutrition for everyone: Basics: Iron and iron deficiency. Available: . Accessed 2013 Sep 9.
    1. Pasricha SR (2012) Should we screen for iron deficiency anaemia? A review of the evidence and recent recommendations. Pathology 44(2): 139–47.
    1. Valberg LS (1980) Plasma ferritin concentrations: their clinical significance and relevance to patient care. Can Med Assoc J 122: 1240–8.
    1. NICE Clinical Knowledge Summaries: Interpreting ferritin levels. Available: . Accessed 2013 Sep 9.
    1. Roked F, Jackson JE, Fuld J, Basheer FT, Chilvers ER, et al. (2011) Pulmonary thromboemboli modifying the natural history of pulmonary arteriovenous malformations. Am J Resp Crit Care Med 183: 828–9.
    1. Santhirapala V, Howard LSGE, Murphy K, Mukherjee B, Busbridge M, et al.. (2013) Oxygen delivery and consumption is preserved in hypoxaemic patients with pulmonary arteriovenous malformations and hereditary haemorrhagic telangiectasia. Hematology Reports 5 (s1) 33–34.
    1. Boulton F (2008) Evidence-based criteria for the care and selection of blood donors, with some comments on the relationship to blood supply, and emphasis on the management of donation-induced iron depletion. Transfus Med 18: 13–27.
    1. Abdullah SM (2011) The effect of repeated blood donations on the iron status of male Saudi blood donors. Blood Transfus 9: 167–71.
    1. Hallberg L (2000) New tools in studies on iron nutrition. Principles, applications and consequences. Scand J Nutr 44: 150–154.
    1. Silva BM, Hosman AE, Devlin HL, Shovlin CL (2013) A questionnaire-based study suggests lifestyle and dietary factors influencing nosebleed severity in hereditary hemorrhagic telangiectasia (HHT). Laryngoscope, 2013 doi:
    1. Pope LER, Hobbs CGL (2005) Epistaxis: an update on current management. Postgrad Med J. 81: 309–14.
    1. Tay HL, Evans JM, McMahon AD, MacDonald TM (1998) Aspirin, nonsteroidal anti-inflammatory drugs, and epistaxis. A regional record linkage case control study. Ann Otol Rhinol Laryngol 107: 671–4.
    1. Saban Y, Amodeo CA, Bouaziz D, Polselli R (2012) Nasal Arterial Vasculature Arch Facial Plast Surg. 14: 429–36.
    1. Rhodes CJ, Howard LS, Busbridge M, Ashby D, Kondili E, et al. (2011) Iron deficiency and raised hepcidin in idiopathic pulmonary arterial hypertension: clinical prevalence, outcomes, and mechanistic insights. J Am Coll Cardiol 58: 300e9.
    1. Girerd B, Montani D, Coulet F, et al. (2010) Clinical outcomes of pulmonary arterial hypertension in patients carrying an ACVRL1 (ALK1) mutation. Am J Respir Crit Care Med 2010 181: 851–61.
    1. Frykman E, Bystrom M, Jansson U, Edberg A, Hansen T (1994) Side effects of iron supplements in blood donors: superior tolerance of heme iron. J Lab Clin Med 123: 561–4.
    1. Royal Pharmaceutical Society of Great Britain and British Medical Association (2012) British National Formulary 63: BMJ Publishing Group, London.
    1. Rimon E, Kagansky N, Kagansky M, Mechnick L, Mashiah T, et al. (2005) Are we giving too much iron? Low-dose iron therapy is effective in octogenarians. Am J Med 118: 1142–7.
    1. Hallberg L (2001) Perspectives on nutritional iron deficiency. Ann Rev Nutrition 21: 1–21.
    1. Aronstam A, Aston DL (1982) A comparative trial of a controlled-release iron tablet preparation (‘Ferrocontin’ Continus) and ferrous fumarate tablets. Pharmatherapeutica 3: 263–7.
    1. National Institute for Health and Clinical Excellence (NICE) (2011) Colorectal cancer. Costing report. Implementing NICE Guidance. Available: . Accessed 2013 Sep 9.
    1. Curtis L (2011). Unit costs of health and social care 2011. PSSRU, Canterbury. Available: . Accessed 2013 September 9.
    1. Hoag J, Terry P, Mitchell S, Reh D, Merlo C (2010) An epistaxis severity score for hereditary hemorrhagic telangiectasia. Laryngoscope 120: 838–43.
    1. Burdett E, Stephens R (2006) Blood transfusion: a practical guide. Br J Hosp Med (Lond) 67: 200–5.
    1. Royal College of Obstetricians and Gynaecologists (2009) Prevention and management of postpartum hemorrhage. Green-top Guideline no 52. Available: . Accessed 2013 Sep 9.
    1. Swain DG, Nightingale PG, Patel JV (2000) Transfusion requirements in femoral neck fracture. Injury 31: 7–10.
    1. Shovlin CL, Guttmacher AE, Buscarini E, Faughan M, Hyland R, et al. (2000) Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet. 91: 66–7.
    1. International Agency for Research on Cancer and World Health Organisation (2010) European Prospective Investigation into Cancer and Nutrition. British Medical Association. Available: . Accessed 2013 September 9.
    1. Welch AA, Luben R, Khaw KT, Bingham SA (2005) The CAFE computer program for nutritional analysis of the EPIC-Norfolk food frequency questionnaire and identification of extreme nutrient values. J Hum Nutr Dietet 18: 99–116.
    1. Bingham SA, Welch AA, McTaggart A, Mulligan AA, Runswick SA, et al. (2001) Nutritional methods in the European Prospective Investigation of Cancer in Norfolk. Public Health Nutr 4: 847–58.
    1. Busbridge M, Griffiths C, Ashby D, Gale D, Jayantha A, et al. (2009) Development of a novel immunoassay for the iron regulatory peptide hepcidin. Br J Biomed Sci 66: 150–7.
    1. Devlin HL, Hosman AE, Shovlin CL (2013) Antiplatelet and anticoagulant agents in hereditary hemorrhagic telangiectasia. N Engl J Med 368: 876–8.
    1. (2004) The National Diet & Nutrition Survey: Adults aged 19 to 64 years. Nutritional status (anthropometry and blood analytes), blood pressure and physical activity. HMSO, Norwich. Available: . Page 63, table 4.1. Accessed 2013 Sep 9.
    1. Franzini CBA, Favarelli C, Brambilla S (2000) Low frequency of elevated serum transferrin saturation in elderly subjects. Clin Chim Acta 298: 181–6.
    1. Tan TC, Crawford DH, Franklin ME, Jaskowski LA, Macdonald GA, et al. (2012) The serum hepcidin:ferritin ratio is a potential biomarker for cirrhosis. Liver Int 32: 1391–9.
    1. Piperno A, Girelli D, Nemeth E, Trombini P, Bozzini C, et al. (2007) Blunted hepcidin response to oral iron challenge in HFE-related hemochromatosis. Blood 110: 4096–4100.
    1. Department of Health (1991) Dietary Reference Values for Food Energy and Nutrients for the United Kingdom. HMSO, London.
    1. Kerr DN, Davidson S (1958) Gastrointestinal intolerance to oral iron preparations. Lancet 2: 489–92.

Source: PubMed

3
Abonnere