Jump to content

Iron deficiency

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by JenOttawa (talk | contribs) at 02:36, 17 September 2023 (→Food sources: iron fortified seasoning- evidence from 2023 systematic review). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

For other uses, see Iron deficiency (disambiguation).

Iron deficiency
Other namesSideropenia, hypoferremia
Iron in heme
SpecialtyHematology

Iron deficiency, or sideropenia, is the state in which a body lacks enough iron to supply its needs. Iron is present in all cells in the human body and has several vital functions, such as carrying oxygen to the tissues from the lungs as a key component of the hemoglobin protein, acting as a transport medium for electrons within the cells in the form of cytochromes, and facilitating oxygen enzyme reactions in various tissues. Too little iron can interfere with these vital functions and lead to morbidity and death.[1]

Total body iron averages approximately 3.8 g in men and 2.3 g in women. In blood plasma, iron is carried tightly bound to the protein transferrin. There are several mechanisms that control iron metabolism and safeguard against iron deficiency. The main regulatory mechanism is situated in the gastrointestinal tract. The majority of iron absorption occurs in the duodenum, the first section of the small intestine. A number of dietary factors may affect iron absorption. When loss of iron is not sufficiently compensated by intake of iron from the diet, a state of iron deficiency develops over time. When this state is uncorrected, it leads to iron-deficiency anemia, a common type of anemia.[1] Before anemia occurs, the medical condition of iron deficiency without anemia is called latent iron deficiency (LID).

Anemia is a condition characterized by inadequate red blood cells (erythrocytes) or hemoglobin. When the body lacks sufficient amounts of iron, production of the protein hemoglobin is reduced. Hemoglobin binds to oxygen, enabling red blood cells to supply oxygenated blood throughout the body. Women of child-bearing age,[2] children, and people with poor diet are most susceptible to the disease. Most cases of iron-deficiency anemia are mild, but if not treated can cause problems like an irregular heartbeat, pregnancy complications, and delayed growth in infants and children that could affect their cognitive development and their behavior.[3]

Signs and symptoms

Deaths due to iron-deficiency anemia per million persons in 2012
  0
  1
  2–3
  4–5
  6–8
  9–12
  13–19
  20–30
  31–74
  75–381
Disability-adjusted life year for iron-deficiency anemia per 100,000 inhabitants in 2004[4]
  no data
  less than 50
  50–100
  100–150
  150–200
  200–250
  250–300
  300–350
  350–400
  400–450
  450–500
  500–1000
  more than 1000

Symptoms of iron deficiency can occur even before the condition has progressed to iron deficiency anemia.

Symptoms of iron deficiency are not unique to iron deficiency (i.e. not pathognomonic). Iron is needed for many enzymes to function normally, so a wide range of symptoms may eventually emerge, either as the secondary result of the anemia, or as other primary results of iron deficiency. Symptoms of iron deficiency include:[citation needed]

Continued iron deficiency may progress to anemia and worsening fatigue. Thrombocytosis, or an elevated platelet count, can also result. A lack of sufficient iron levels in the blood is one reason that some people cannot donate blood.

Signs and symptoms in children


Iron requirements in young children to teenagers

Age group Recommended amount of iron a day[7]
7–12 months 11 mg
1–3 years 7 mg
4–8 years 10 mg
9–13 years 8 mg
14–18 years, girls 15 mg
14–18 years, boys 11 mg

Causes

Though genetic defects causing iron deficiency have been studied in rodents, there are no known genetic disorders of human iron metabolism that directly cause iron deficiency.

Athletics

Possible reasons that athletics may contribute to lower iron levels includes mechanical hemolysis (destruction of red blood cells from physical impact), loss of iron through sweat and urine, gastrointestinal blood loss, and haematuria (presence of blood in urine).[9][10] Although small amounts of iron are excreted in sweat and urine, these losses can generally be seen as insignificant even with increased sweat and urine production, especially considering that athletes' bodies appear to become conditioned to retain iron better.[9] Mechanical hemolysis is most likely to occur in high-impact sports, especially among long-distance runners who experience "foot-strike hemolysis" from the repeated impact of their feet with the ground. Exercise-induced gastrointestinal bleeding is most likely to occur in endurance athletes. Haematuria in athletes is most likely to occur in those that undergo repetitive impacts on the body, particularly affecting the feet (such as running on a hard road, or Kendo) and hands (e.g. Conga or Candombe drumming). Additionally, athletes in sports that emphasize weight loss (e.g. ballet, gymnastics, marathon running, and cycling) as well as sports that emphasize high-carbohydrate, low-fat diets, may be at an increased risk for iron deficiency.[9][10]

Inadequate intake

A U.S. federal survey of food consumption determined that for women and men over the age of 19, average iron consumption from foods and beverages was 13.1 and 18.0 mg/day, respectively. For women, 16% in the age range 14–50 years consumed less than the Estimated Average Requirement (EAR), for men ages 19 and up, fewer than 3%.[11] Consumption data were updated in a 2014 U.S. government survey and reported that for men and women ages 20 and older the average iron intakes were, respectively, 16.6 and 12.6 mg/day.[12] People in the U.S. usually obtain adequate amounts of iron from their diets. However, subgroups like infants, young children, teenaged girls, pregnant women, and premenopausal women are at risk of obtaining less than the EAR.[13] Socio-economic and racial differences further affect the rates of iron deficiency.[13]

Bioavailability

Iron is needed for bacterial growth making its bioavailability an important factor in controlling infection.[14] Blood plasma as a result carries iron tightly bound to transferrin, which is taken up by cells by endocytosing transferrin, thus preventing its access to bacteria.[15]: 30  Between 15 and 20 percent of the protein content in human milk consists of lactoferrin[16] that binds iron. As a comparison, in cow's milk, this is only 2 percent. As a result, breast-fed babies have fewer infections.[15] Lactoferrin is also concentrated in tears, saliva and at wounds to bind iron to limit bacterial growth. Egg white contains 12% conalbumin to withhold it from bacteria that get through the egg shell (for this reason, prior to antibiotics, egg white was used to treat infections).[15]: 29 

To reduce bacterial growth, plasma concentrations of iron are lowered in a variety of systemic inflammatory states due to increased production of hepcidin which is mainly released by the liver in response to increased production of pro-inflammatory cytokines such as interleukin-6. This functional iron deficiency will resolve once the source of inflammation is rectified; however, if not resolved, it can progress to anaemia of chronic inflammation. The underlying inflammation can be caused by fever,[17] inflammatory bowel disease, infections, chronic heart failure (CHF), carcinomas, or following surgery.

Reflecting this link between iron bioavailability and bacterial growth, the taking of oral iron supplements in excess of 200 mg/day causes a relative overabundance of iron that can alter the types of bacteria that are present within the gut. There have been concerns regarding parenteral iron being administered whilst bacteremia is present, although this has not been borne out in clinical practice. A moderate iron deficiency, in contrast, can provide protection against acute infection, especially against organisms that reside within hepatocytes and macrophages, such as malaria and tuberculosis. This is mainly beneficial in regions with a high prevalence of these diseases and where standard treatment is unavailable.[citation needed]

Diagnosis

  • A complete blood count can reveal microcytic anemia,[18] although this is not always present – even when iron deficiency progresses to iron-deficiency anemia.
  • Low serum ferritin (see below)
  • Low serum iron
  • High TIBC (total iron binding capacity), although this can be elevated in cases of anemia of chronic inflammation.
  • It is possible that the fecal occult blood test might be positive, if iron deficiency is the result of gastrointestinal bleeding; although the sensitivity of the test may mean that in some cases it will be negative even with enteral blood loss.

As always, laboratory values have to be interpreted with the lab's reference values in mind and considering all aspects of the individual clinical situation.

Serum ferritin can be elevated in inflammatory conditions; so a normal serum ferritin may not always exclude iron deficiency, and the utility is improved by taking a concurrent C-reactive protein (CRP). The level of serum ferritin that is viewed as "high" depends on the condition. For example, in inflammatory bowel disease the threshold is 100, where as in chronic heart failure (CHF) the levels are 200.[citation needed]

Treatment

Before commencing treatment, there should be definitive diagnosis of the underlying cause for iron deficiency. This is particularly the case in older patients, who are most susceptible to colorectal cancer and the gastrointestinal bleeding it often causes. In adults, 60% of patients with iron-deficiency anemia may have underlying gastrointestinal disorders leading to chronic blood loss.[19] It is likely that the cause of the iron deficiency will need treatment as well.

Upon diagnosis, the condition can be treated with iron supplements. The choice of supplement will depend upon both the severity of the condition, the required speed of improvement (e.g. if awaiting elective surgery) and the likelihood of treatment being effective (e.g. if the patient has underlying IBD, is undergoing dialysis, or is having ESA therapy).

Examples of oral iron that are often used are ferrous sulfate, ferrous gluconate, or amino acid chelate tablets. Recent research suggests the replacement dose of iron, at least in the elderly with iron deficiency, may be as little as 15 mg per day of elemental iron.[20]

Low-certainty evidence suggests that IBD-related anemia treatment with Intravenous (IV) iron infusion may be more effective than oral iron therapy, with fewer people needing to stop treatment early due to adverse effects. [21] The type of iron preparation may be an important determinant of clinical benefit. Moderate-certainty evidence suggests response to treatment may be higher when IV ferric carboxymaltose, rather than IV iron sucrose preparation is used, despite very-low certainty evidence of increased adverse effects, including bleeding, in those receiving ferric carboxymaltose treatment. [21]

Ferric maltol, marketed as Accrufer and Ferracru, is available in oral and IV preparations. When used as a treatment for IBD-related anemia, very low certainty evidence suggests a marked benefit with oral ferric maltol compared with placebo. However it was unclear whether the IV preparation was more effective than oral ferric maltol. [22]

A Cochrane review of controlled trials comparing intravenous (IV) iron therapy with oral iron supplements in people with chronic kidney disease, found low-certainty evidence that people receiving IV-iron treatment were 1.71 times as likely to reach their target hemoglobin levels. [23]Overall, hemoglobin was 0.71g/dl higher than those treated with oral iron supplements. Iron stores in the liver, estimated by serum ferritin, were also 224.84 µg/L higher in those receiving IV-iron. [23]However there was also low-certainty evidence that allergic reactions were more likely following IV-iron therapy. It was unclear whether type of iron therapy administration affects the risk of death from any cause, including cardiovascular, nor whether it may alter the number of people who may require a blood transfusion or dialysis. [23]

Food sources

Mild iron deficiency can be prevented or corrected by eating iron-rich foods and by cooking in an iron skillet. Because iron is a requirement for most plants and animals, a wide range of foods provide iron. Good sources of dietary iron have heme iron, as this is most easily absorbed and is not inhibited by medication or other dietary components. Two examples are red meat and poultry.[24][25] Non-heme sources do contain iron, though it has reduced bioavailability. Examples are lentils, beans, leafy vegetables, pistachios, tofu, fortified bread, and fortified breakfast cereals.

Iron from different foods is absorbed and processed differently by the body; for instance, iron in meat (heme iron source) is more easily absorbed than iron in grains and vegetables ("non-heme" iron sources).[26] Minerals and chemicals in one type of food may also inhibit absorption of iron from another type of food eaten at the same time.[27] For example, oxalates and phytic acid form insoluble complexes which bind iron in the gut before it can be absorbed.

Because iron from plant sources is less easily absorbed than the heme-bound iron of animal sources, vegetarians and vegans should have a somewhat higher total daily iron intake than those who eat meat, fish or poultry.[28] Legumes and dark-green leafy vegetables like broccoli, kale and Asian greens are especially good sources of iron for vegetarians and vegans. However, spinach and Swiss chard contain oxalates which bind iron, making it almost entirely unavailable for absorption.[citation needed] Iron from non-heme sources is more readily absorbed if consumed with foods that contain either heme-bound iron or vitamin C. This is due to a hypothesised "meat factor" which enhances iron absorption.[29] The benefits of eating seasonings or condiments that have been fortified with iron for people with iron deficiencies are not clear.[30] There is some evidence that iron fortified condiments or seasonings may help reduce an iron deficiency, however, whether this improves a person's health and prevents the person from developing anemia is not clear.[30]

Following are two tables showing the richest foods in heme and non-heme iron.[31][unreliable source?] In both tables, food serving sizes may differ from the usual 100g quantity for relevancy reasons[clarify]. Arbitrarily, the guideline is set at 18 mg, which is the USDA Recommended Dietary Allowance for women aged between 19 and 50.[32]

Richest foods in heme iron
Food Serving size Iron % guideline
clam[a] 100g 28 mg 155%
pork liver 100g 18 mg 100%
lamb kidney 100g 12 mg 69%
cooked oyster 100g 12 mg 67%
cuttlefish 100g 11 mg 60%
lamb liver 100g 10 mg 57%
octopus 100g 9.5 mg 53%
mussel 100g 6.7 mg 37%
beef liver 100g 6.5 mg 36%
beef heart 100g 6.4 mg 35%
Richest foods in non-heme iron
Food Serving size Iron % guideline
raw yellow beans 100g 7 mg 35%
spirulina 15g 4.3 mg 24%
falafel 140g 4.8 mg 24%
soybean kernels 125ml=1/2cup 4.6 mg 23%
spinach 125g 4.4 mg 22%
lentil 125ml=1/2cup 3.5 mg 17.5%
treacle (CSR Australia) 20ml=1Tbsp 3.4 mg 17%
molasses (Bluelabel Australia) 20ml=1Tbsp 1.8 mg 9%
candied ginger root 15g~3p 1.7 mg 8.5%
toasted sesame seeds 10g 1.4 mg 7%
cocoa (dry powder) 5g~1Tbsp .8 mg 4%

Food recommendations for children

Children at 6 months should start having solid food that contains enough iron, which could be found in both heme and non-heme iron.[36]

Heme iron:

  • Red meat (for example, beef, pork, lamb, goat, or venison)
  • Fatty fish
  • Poultry (for example, chicken or turkey)
  • Eggs

Non-heme iron:

  • Iron-fortified infant cereals
  • Tofu
  • Beans and lentils
  • Dark green leafy vegetables

Iron deficiency can have serious health consequences that diet may not be able to quickly correct; hence, an iron supplement is often necessary if the iron deficiency has become symptomatic.

Blood transfusion

Blood transfusion is sometimes used to treat iron deficiency with hemodynamic instability.[37] Sometimes transfusions are considered for people who have chronic iron deficiency or who will soon go to surgery, but even if such people have low hemoglobin, they should be given oral treatment or intravenous iron.[37]

Intravenous iron therapy for non-anaemic, iron-deficient adults

Current evidence is limited to base any recommendations that intravenous iron therapy is beneficial for treating non-anaemic, iron-deficient adults.[38] Further research in this area is needed as current body of evidence is very low quality.  

Cancer research

The presence of Helicobacter pylori in the stomach can cause inflammation and can lower the threshold for the development of gastric cancer. In the setting of iron deficiency, H. pylori causes more severe inflammation and the development of premalignant lesions.[39] This inflammatory effect appears to be mediated, in part, through altered bile acid production including an increase in deoxycholic acid, a secondary bile acid implicated in colon cancer and other gastrointestinal cancers.[39]

See also

Notes

  1. ^ Iron content in clams can vary considerably between types and modes of preparation, and the presence of aluminium could reduce iron bioavailability.[33] The bioaccumulation of heavy metals in clams from highly contaminated areas may make regular consumption unsafe in the long term.[34][35]

References

  1. ^ a b "Recommendations to prevent and control iron deficiency in the United States. Centers for Disease Control and Prevention". MMWR. Recommendations and Reports. 47 (RR-3): 1–29. April 1998. PMID 9563847.
  2. ^ "Women of reproductive age (15-49 years) population (thousands)". www.who.int.
  3. ^ "Iron and Iron Deficiency". Centers for Disease Control and Prevention. 23 February 2011. Archived from the original on 8 September 2014. Retrieved 12 August 2014.
  4. ^ "Mortality and Burden of Disease Estimates for WHO Member States in 2002" (xls). World Health Organization. 2002.
  5. ^ Wintergerst ES, Maggini S, Hornig DH (2007). "Contribution of selected vitamins and trace elements to immune function" (PDF). Annals of Nutrition & Metabolism. 51 (4): 301–23. doi:10.1159/000107673. PMID 17726308. S2CID 1108612.
  6. ^ Rangarajan S, D'Souza GA (April 2007). "Restless legs syndrome in Indian patients having iron deficiency anemia in a tertiary care hospital". Sleep Medicine. 8 (3): 247–51. doi:10.1016/j.sleep.2006.10.004. PMID 17368978.
  7. ^ "Is your child getting enough iron?". Mayo Clinic. Retrieved 26 April 2019.
  8. ^ Badal S, Her YF, Maher LJ (September 2015). "Nonantibiotic Effects of Fluoroquinolones in Mammalian Cells". The Journal of Biological Chemistry. 290 (36): 22287–97. doi:10.1074/jbc.M115.671222. PMC 4571980. PMID 26205818.
  9. ^ a b c Nielsen P, Nachtigall D (October 1998). "Iron supplementation in athletes. Current recommendations". Sports Medicine. 26 (4): 207–16. doi:10.2165/00007256-199826040-00001. PMID 9820921. S2CID 25517866.[dead link‍]
  10. ^ a b Chatard JC, Mujika I, Guy C, Lacour JR (April 1999). "Anaemia and iron deficiency in athletes. Practical recommendations for treatment". Sports Medicine. 4. 27 (4): 229–40. doi:10.2165/00007256-199927040-00003. PMID 10367333. S2CID 32504228.
  11. ^ Moshfegh A, Goldman J, Cleveland L (September 2005). "Table A12: Iron" (PDF). What we eat in America, NHANES 2001-2002: usual nutrient intakes from food compared to dietary reference intakes. National Health and Nutrition Examination Survey (NHANES) (Report). US Department of Agriculture, Agricultural Research Service. Archived from the original on 6 January 2015.
  12. ^ "What We Eat In America, NHANES 2013-2014" (PDF). National Health and Nutrition Examination Survey (NHANES). US Department of Agriculture, Agricultural Research Service.
  13. ^ a b "Iron". Fact Sheet for Health Professionals. Office of Dietary Supplements. National Institutes of Health. February 2020.
  14. ^ Kluger MJ, Rothenburg BA (January 1979). "Fever and reduced iron: their interaction as a host defense response to bacterial infection". Science. 203 (4378): 374–6. Bibcode:1979Sci...203..374K. doi:10.1126/science.760197. PMID 760197.
  15. ^ a b c Nesse RM, Williams GC (1996). Why We Get Sick: The New Science of Darwinian Medicine (First ed.). New York: Vintage Books. ISBN 978-0-679-74674-4.
  16. ^ Lien EL (1997). "Modification of Infant Formula: The Case ofLactoferrin" (PDF). In Hutchens TW, Lönnerdal B (eds.). Lactoferrin: Interactions and Biological Functions. Experimental Biology and Medicine. Totowa, NJ: Humana Press. p. 379. doi:10.1007/978-1-4612-3956-7_24. ISBN 978-1-4612-3956-7.
  17. ^ Weinberg ED (January 1984). "Iron withholding: a defense against infection and neoplasia". Physiological Reviews. 64 (1): 65–102. doi:10.1152/physrev.1984.64.1.65. PMID 6420813.
  18. ^ Longmore M, Wilkinson IB, Rajagoplan S (2004). Oxford Handbook of Clinical Medicine (6th ed.). Oxford University Press. pp. 626–628. ISBN 0-19-852558-3.
  19. ^ Rockey DC, Cello JP (December 1993). "Evaluation of the gastrointestinal tract in patients with iron-deficiency anemia". The New England Journal of Medicine. 329 (23): 1691–5. doi:10.1056/NEJM199312023292303. PMID 8179652.
  20. ^ Rimon E, Kagansky N, Kagansky M, Mechnick L, Mashiah T, Namir M, Levy S (October 2005). "Are we giving too much iron? Low-dose iron therapy is effective in octogenarians". The American Journal of Medicine. 118 (10): 1142–7. doi:10.1016/j.amjmed.2005.01.065. PMID 16194646.
  21. ^ a b Gordon, Morris; Sinopoulou, Vassiliki; Iheozor-Ejiofor, Zipporah; Iqbal, Tariq; Allen, Patrick; Hoque, Sami; Engineer, Jaina; Akobeng, Anthony K (2021). "Interventions for treating iron deficiency anaemia in inflammatory bowel disease". Cochrane Database of Systematic Reviews. 1 (1): CD013529. doi:10.1002/14651858.CD013529.pub2. PMC 8092475. PMID 33471939.
  22. ^ Gordon, Morris; Sinopoulou, Vassiliki; Iheozor-Ejiofor, Zipporah; Iqbal, Tariq; Allen, Patrick; Hoque, Sami; Engineer, Jaina; Akobeng, Anthony K (2021). "Interventions for treating iron deficiency anaemia in inflammatory bowel disease". Cochrane Database of Systematic Reviews. 1 (1): CD013529. doi:10.1002/14651858.CD013529.pub2. PMC 8092475. PMID 33471939.
  23. ^ a b c O'Lone, Emma L; Hodson, Elisabeth M; Nistor, Ionut; Bolignano, Davide; Webster, Angela C; Craig, Jonathan C (2019). Cochrane Kidney and Transplant Group (ed.). "Parenteral versus oral iron therapy for adults and children with chronic kidney disease". Cochrane Database of Systematic Reviews. 2019 (2): CD007857. doi:10.1002/14651858.CD007857.pub3. PMC 6384096. PMID 30790278.
  24. ^ Defoliart G (1992). "Insects as Human Food". Crop Protection. 11 (5): 395–99. doi:10.1016/0261-2194(92)90020-6.
  25. ^ Bukkens SG (1997). "The Nutritional Value of Edible Insects". Ecol. Food. Nutr. 36 (2–4): 287–319. doi:10.1080/03670244.1997.9991521.
  26. ^ "Iron deficiency". UK Food Standards Agency. Archived from the original on 8 August 2006.
  27. ^ "Iron in diet". MedlinePlus. U.S. National Library of Medicine.
  28. ^ Reed M. "Iron in the vegan diet". The Vegetarian Resource Group.
  29. ^ "Iron". The Merck Manuals Online Medical Library. Archived from the original on 17 October 2015. Retrieved 27 October 2015.
  30. ^ a b Jalal, Chowdhury SB; De-Regil, Luz Maria; Pike, Vanessa; Mithra, Prasanna (1 September 2023). Cochrane Public Health Group (ed.). "Fortification of condiments and seasonings with iron for preventing anaemia and improving health". Cochrane Database of Systematic Reviews. 2023 (9). doi:10.1002/14651858.CD009604.pub2. PMC 10472972. PMID 37665781.
  31. ^ "Iron rich foods". Rich Foods. Archived from the original on 18 May 2017.
  32. ^ "Dietary Reference Intakes: Recommended Intakes for Individuals" (PDF). National Academy of Sciences. Institute of Medicine. Food and Nutrition Board. Archived from the original (PDF) on 6 September 2013.
  33. ^ Lai JF, Dobbs J, Dunn MA (February 2012). "Evaluation of clams as a food source of iron: Total iron, heme iron, aluminum, and in vitro iron bioavailability in live and processed clams". Journal of Food Composition and Analysis. 25 (1): 47–55. doi:10.1016/j.jfca.2011.07.004.
  34. ^ Hossen MF, Hamdan S, Rahman MR (2015). "Review on the Risk Assessment of Heavy Metals in Malaysian Clams". TheScientificWorldJournal. 2015: 905497. doi:10.1155/2015/905497. PMC 4427851. PMID 26060840.
  35. ^ Fang ZQ, Cheung RY, Wong MH (January 2003). "Heavy metals in oysters, mussels and clams collected from coastal sites along the Pearl River Delta, South China". Journal of Environmental Sciences. 15 (1): 9–24. PMID 12602597.
  36. ^ CDC (3 December 2018). "Iron - Infant and Toddler Nutrition". Centers for Disease Control and Prevention. Retrieved 26 April 2019.
  37. ^ a b American Association of Blood Banks (24 April 2014), "Five Things Physicians and Patients Should Question", Choosing Wisely: an initiative of the ABIM Foundation, American Association of Blood Banks, archived from the original on 24 September 2014, retrieved 25 July 2014, which cites
  38. ^ Miles LF, Litton E, Imberger G, Story D (December 2019). "Intravenous iron therapy for non-anaemic, iron-deficient adults". The Cochrane Database of Systematic Reviews. 12 (12): CD013084. doi:10.1002/14651858.cd013084.pub2. PMC 6924972. PMID 31860749.
  39. ^ a b Noto JM, Piazuelo MB, Shah SC, Romero-Gallo J, Hart JL, Di C, Carmichael JD, Delgado AG, Halvorson AE, Greevy RA Jr, Wroblewski LE, Sharma A, Newton AB, Allaman MM, Wilson KT, Washington MK, Calcutt MW, Schey KL, Cummings BP, Flynn CR, Zackular JP, Peek RM Jr. Iron deficiency linked to altered bile acid metabolism promotes Helicobacter pylori-induced inflammation-driven gastric carcinogenesis. J Clin Invest. 2022 Mar 22:e147822. doi: 10.1172/JCI147822. Epub ahead of print. PMID 35316215

Further reading

. Zeglam A, Abugrara A, Kabuka M. Autosomal-recessive iron deficiency anemia, dystonia and hypermanganesemia caused by new variant mutation of the manganese transporter gene SLC39A14. Acta Neurol Belg. 2019 Sep;119(3):379-384. doi: 10.1007/s13760-018-1024-7. Epub 2018 Sep 19. PMID 30232769.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Iron_deficiency&oldid=1175737454"