Imerslund–Gräsbeck syndrome, also known as Imerslund–Najman–Gräsbeck syndrome, Imerslund–Gräsbeck disease (IGS or INGS), Imerslund syndrome, congenital cobalamin malabsorption or autosomal recessive megaloblastic anemia (MGA1), is a rare autosomal recessive, familial form of vitamin B12 deficiency caused by malfunction of the "Cubam" receptor located in the terminal ileum. This receptor is composed of two proteins, amnionless (AMN), and cubilin. A defect in either of these protein components can cause this syndrome. This is a rare disease, with a prevalence about 1 in 200,000,[1] and is usually seen in patients of European ancestry.
Vitamin B12 is an important vitamin needed for bone marrow functioning, the deficit of which causes decreased marrow output and anemia. Vitamin B12 has two forms, one of which, along with folate, is important in DNA synthesis. Vitamin B12 is sensitive to acid deformation in the stomach, so a molecule called haptocorrin (R-factor), protects it in the stomach. In the small bowel, a molecule named intrinsic factor (IF), allows vitamin B12 to be absorbed in the ileum. IGS is caused by a mutation in the receptors located in the terminal portion of ileum. This is a very rare, and unlikely cause of vitamin B12 deficiency but is a cause nonetheless.
Contents
- 1 Signs and symptoms
- 2 Genetics
- 3 Pathogenesis
- 4 Treatment
- 5 Epidemiology
- 6 History
- 7 References
- 8 Sources
Signs and symptoms
Defined as those seen in any macrocytic, megaloblastic anemia:
- Anemia: causing fatigue, conjuctival pallor, pale complexion, and in some cases, a mild icterus (yellowing of the eye).
- Glossitis ("shiny tongue"): shiny, glossy tongue.
- Cheilosis (stomatitis): Inflammation of the edges of the lips and the oral mucosa.
- Tabes dorsalis ("subacute combined degeneration of the spinal cord"): This involves the posterior section of the spinal cord and therefore involves proprioception (sense of position), touch, sense of vibration and in severe cases the lateral corticospinal tract, causing spastic paralysis of the limbs.
- Peripheral neuropathy: tingling sensation in the arms and legs.
- Pancytopenia: decreased number of blood cells of all lineages (RBCs,leucocytes,platelets), due to decreased bone marrow production.
- Methylmalonyl CoA-emia: defined as blood having and unusually high concentration of methylmalonyl CoA.
- Peripheral findings such as hypersegmented neutrophils and large RBCs on high field view of the blood smears.
- Laboratory findings indicating increased MCV (Mean Corpuscular Volume), decreased Hgb/Hct (indicating anemia), and decreased value of vitamin B12 in the blood.
- Proteinuria: protein found in the urine detected by analysis or by dipstick.
- Reversal of all symptoms except neurological symptoms, by IV injection of vitamin B12.
- Schilling test indicating no radioactive vitamin B12 in the urine. (This test has dropped out of favor and should not be tried in patients with any form of renal failure).
Genetics
The disease is autosomal recessive, and can therefore skip generations. Mutations in either amnionless (AMN) or cubilin can be the culprit. Due to its autosomal recessive pattern of inheritance, affected individuals (persons possessing a homozygous recessive genotype) need to undergo genetic counselling to identify risk of family members who might be heterozygous genetic carriers. Certain mutations on the CUBN or AMN (genes that encode cubilin and amnionless respectively) have been identified through genetic analysis, and ethnic susceptibility of some of the mutations were indicated from the current research. [2] [3] It has been further suggested that mutations on CUBN were restricted to exon 1-28 which encoded amnionless binding domains (EGF) and IF-Cbl binding region of cubilin,while AMN mutations primarily clustered in intron 8-11 and transmembrane domain in exon 10. [4] Some interesting aspects of particular mutations were also elucidated by the researchers, for example, CUBN mutation c.3890C>T; p.Pro1297Leu,was considered to be a Finnish founder mutation presenting mostly in homozygous status, while an AMN mutation c.208-2A>G, which was thought to account for 15% IGS cases around the world, was postulated as an ancient founder mutation that can trace back to approximately 13,600 years ago. [5] [6]
Pathogenesis
Vitamin B12, is an essential water-soluble vitamin found in animal products (such as liver, meat, fish, and dairy products).[7] Vitamin B12 is not found in plant sources; a vegetarian diet can be a risk factor for vitamin B12 deficiency. Normal daily intake of vitamin B12 is 7–30 micro gram, cooking has minimal effect on the structure of this vitamin. The minimal daily adult requirement is 1–3 micro gram, and the human body is able to store at any one time about 2–3 milligram, which is sufficient for at least 2 years of impeccable functioning before the source is depleted. In terms of absorption, no more than 2–3 microgram of vitamin B12 can be absorbed on a daily basis, with some 5–10 microgram of the vitamin B12 involved in enterohepatic circulation.[7] This is in general a principal characteristic of water-soluble vitamins, in that no matter the oral intake, there is a certain threshold for intestinal absorption hence, low or non-existent chance of intoxication, as opposed to fat-soluble vitamins.
Vitamin B12 has a major function in the nuclear replication of the DNA. It is therefore logical that its deficiency causes decrease bone marrow production, one of the most common manifestations of which is decreased red blood cell production or as it is referred to medically, anemia. Vitamin B12 however has two major forms in the human body:
- Deoxyadenosyl B12 or as it is sometimes referred to Ado B12: Ado B12 is essential for acid-base maintenance of the blood, simply because Ado B12 is the catalyst that assists the conversion of, Methylmalonyl CoA, into Succinyl CoA. In absence of vitamin B12, levels of Methylmalonyl CoA increase, and this is in fact a great way to distinguish folate deficiency macrocytic anemia, from vitamin B12 anemia. The following is the reaction in which Ado B12, plays a pivotal role:
Propionyl CoA → Methylmalonyl CoA → Succinyl CoA [7]
- Methyl B12: This form of vitamin B12 is essential for conversion of Methy-THF (methyl tetrahydrofolate) into THF, and methyl (CH3). The methyl group, is then used to add a carbon, to homocysteine, converting it into Methionine. Methionine is further converted to S-adenosyl methionine, which in turn gives of the extra carbon it received from THF, now to a DNA nucleotide, becoming S-adenosyl homcysteine. S-adenosyl Homocysteine, further loses its "S-adenosyl" attachment, to become homocysteine, and the cycle repeats yet again!
Methyl THF → CH3 + THF
↓
Homocysteine → Methionine
S-adenosyl ← ↑ ↓ ← S-adenosyl
S-adenosyl Homocysteine ← S-adenosyl Methionine
↓
CH3
↓
DNA → Methyl-DNA
It is therefore understood that vitamin B12 is involved in complex DNA synthesis, along with folate, as well as in acid-base metabolism. To understand the basic pathophysiology of Imerslund-Gräsbeck syndrome, it is imperative to understand the absorption of vitamin B12. The following lists principal events that lead to absorption of vitamin B12 along the GI tract:
- Oral cavity: vitamin B12 containing food is ingested. Salivary glands produce haptocorrin, which binds vitamin B12, creating a "vitamin B12-Haptocorrin complex". This complex is then ingested via esophageal peristalsis into the stomach.
- Stomach: vitamin B12-Haptocorrin, survives the low pH, highly osmotic environment of the stomach. Parietal cells produce hydrochloric acid (the effect of which Haptocorrin protects vitamin B12 from), and also intrinsic factor (IF). Intrinsic factor also has a high binding affinity for vitamin B12, but because that position is already filled by Haptocorrin, free intrinsic factor, and "Haptocorrin-vitamin B12" complex, empty from the stomach into the duodenum.
- duodenum: Pancreatic juice, produced by the pancreas, contains pancreatic proteases that break the haptocorrin, degrading it and freeing the vitamin B12. Once free, vitamin B12, binds with intrinsic factor (IF), to produce an "IF-vitamin B12" complex.
- Ileum: Cubam, a receptor found in the terminal portion of the ileum is a specialized receptor complex. The complex is responsible for the recognition of the "vitamin B12-IF" complex and initiating the endocytosis of the complex, resulting in absorption.
Cubam is composed of two molecules, amnionless (AMN) and cubilin.[8][9] Cubilin is a multi-ligand protein that contains eight epidermal growth factor (EGF) repeats and 27 CUB domains, from which the four active domains (CUB5-8) collectively get involved in binding interaction with the IF-Cbl complex. [10] Whereas, amnionless is an apical transmembrane protein which is expressed in both intestine and kidney, and it seems to assist the subcellular localization and endocytosis of the cubilin by binding to its amino-terminal residues.[11] [12] Cubilin specializes in recognition of the "vitamin B12-IF" complex and attaches to it, while amnionless (AMN) is responsible for initiation of the endocytosis of complex and the subsequent absorption of vitamin B12. It is at this point that the pathology of IGS syndrome occurs by preventing the absorption of vitamin B12, and can be caused by a mutation in either the amnionless (AMN) portion or the cubilin portion of the receptor.[1]
Treatment
Since the essential pathology is due to the inability to absorb vitamin B12 from the bowels, the solution is therefore injection of IV vitamin B12. Timing is essential, as some of the side effects of vitamin B12 deficiency are reversible (such as RBC indices, peripheral RBC smear findings such as hypersegmented neutrophils, or even high levels of methylmalonyl CoA), but some side effects are irreversible as they are of a neurological source (such as tabes dorsalis, and peripheral neuropathy). High suspicion should be exercised when a neonate, or a pediatric patient presents with anemia, proteinuria, sufficient vitamin B12 dietary intake, and no signs of pernicious anemia.
Epidemiology
This is a rare disease with prevalence about 1 in 200,000[1] to 1 in 600,000.[13] Studies showed that mutations in CUBN or AMN clustered particularly in the Scandinavian countries and the Eastern Mediterranean regions. Founder effect, higher clinical awareness to IGS, and frequent consanguineous marriages all play a role in the higher prevalence of IGS among these populations [14] [15] [16]
History
The syndrome is the result of the collective work done by a Norwegian pediatrician, Olga Imerslund,[17] a Finnish physician and clinical biochemist, Armas Ralph Gustaf Gräsbeck, and Emil Najman, a pediatrician from Croatia.
References
- ^ a b c Grasbeck R (2006). "Imerslund-Gräsbeck syndrome (selective vitamin B12 malabsorption with proteinuria)". Orphanet Journal of Rare Diseases 1 (1): 17. doi:10.1186/1750-1172-1-17. PMC 1513194. PMID 16722557.
- ^ Tanner, S. M., Sturm, A., Baack, E. C., Liyanarachchi, S., & De La Chapella, A. (2012). Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. Orphanet Journal of Rare diseases, 7(1), 56.
- ^ Tanner, S. M., Li, Z., Bisson, R., Acar, C., Oner, C., Oner, R., Cetin, M., Abdelaal, M. A., . . . De La Chapella, A. (2004). Genetically Heterogeneous Selective Intestinal Malabsorption of Vitamin B12: Founder Effects, Consanguinity, and High Clinical Awareness Explain Aggregations in Scandinavia and the Middle Ease. Human Mutation, 23, 327-333.
- ^ Tanner, S. M., Sturm, A., Baack, E. C., Liyanarachchi, S., & De La Chapella, A. (2012). Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. Orphanet Journal of Rare diseases, 7(1), 56.
- ^ Beech, C. M., Liyanarachchi, S., Shah, N. P., Sturm, A., Sadiq, M. F., De La Chapelle, A., & Tanner, S. M. (2011). Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities. Orphanet Journal of Rare Diseases, 6(1), 74.
- ^ Tanner, S. M., Sturm, A., Baack, E. C., Liyanarachchi, S., & De La Chapella, A. (2012). Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. Orphanet Journal of Rare diseases, 7(1), 56.
- ^ a b c Pettit, John D.; Paul Moss (2006). Essential Haematology 5e (Essential). Blackwell Publishing Professional. pp. 44–6. ISBN 1-4051-3649-9.
- ^ Pedersen GA, Chakraborty S, Steinhauser AL, Traub LM, Madsen M (May 2010). "AMN directs endocytosis of the intrinsic factor-vitamin B(12) receptor cubam by engaging ARH or Dab2". Traffic 11 (5): 706–20. doi:10.1111/j.1600-0854.2010.01042.x. PMC 2964065. PMID 20088845.
- ^ Quadros EV (January 2010). "Advances in the understanding of cobalamin assimilation and metabolism". Br. J. Haematol. 148 (2): 195–204. doi:10.1111/j.1365-2141.2009.07937.x. PMC 2809139. PMID 19832808.
- ^ Mathews, F. S., Gordon, M. M., Chen, Z., Rajashankar, K. R., Ealick, S. E., Alpers, D. H., & Sukumar, N. (2007). Crystal structure of human intrinsic factor: Cobalamin complex at 2.6-A resolution. Proceedings of the National Academy of Sciences of the United States of America, 104(44), 17311-17316.
- ^ Fyfe, J., Madsen, M., Hojrup, P., Christensen, E. I., Tanner, S. M., De La Chapelle, M., He, Q., & Moestrup, S. K. (2004). The functional cobalamin (vitamin B12)–intrinsic factor receptor is a novel complex of cubilin and amnionless. Blood, 103(5), 1573-1579.
- ^ Grasbeck, R. (2006). Imerslund-Grasbeck syndrome (selective vitamin B12 malabsorption with proteinuria). Orphanet Journal of Rare diseases, 1(1), 17.
- ^ De Filippo, Gianpaolo; Rendina, Domenico; Rocco, Vincenzo; Esposito, Teresa; Gianfrancesco, Fernando; Strazzullo, Pasquale (2013). "Imerslund-Grasbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN". Italian Journal of Pediatrics 39 (1): 58. doi:10.1186/1824-7288-39-58. PMC 3848621. PMID 24044590.
- ^ Beech, C. M., Liyanarachchi, S., Shah, N. P., Sturm, A., Sadiq, M. F., De La Chapelle, A., & Tanner, S. M. (2011). Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities. Orphanet Journal of Rare Diseases, 6(1), 74.
- ^ Tanner, S. M., Sturm, A., Baack, E. C., Liyanarachchi, S., & De La Chapella, A. (2012). Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. Orphanet Journal of Rare diseases, 7(1), 56.
- ^ Tanner, S. M., Li, Z., Bisson, R., Acar, C., Oner, C., Oner, R., Cetin, M., Abdelaal, M. A., . . . De La Chapella, A. (2004). Genetically Heterogeneous Selective Intestinal Malabsorption of Vitamin B12: Founder Effects, Consanguinity, and High Clinical Awareness Explain Aggregations in Scandinavia and the Middle Ease. Human Mutation, 23, 327-333.
- ^ "Who named it --Olga Imerslund"
Sources
- Tanner, S. M.; Li, Z.; Bisson, R.; Acar, C.; Oner, C.; Oner, R.; Cetin, M.; Abdelaal, M. A.; Ismail, E. A.; Lissens, W.; Krahe, R.; Broch, H.; Gräsbeck, R.; De la Chapella, A. (2004). "Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East". Human Mutation 23 (4): 327–333. PMID 15024727.
- Tanner, S. M.; Sturm, A. C.; Baack, E. C.; Liyanarachchi, S.; De la Chapelle, A. (2012). "Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns" (PDF). Orphanet Journal of Rare Diseases 7 (56). doi:10.1186/1750-1172-7-56.