Skip to content
2000
Volume 4, Issue 1
  • ISSN: 2666-2906
  • E-ISSN: 2666-2914

Abstract

Vitamin B12 (cobalamin) is a water-soluble vitamin. It is a crucial vitamin for the health of humans, contributing immensely to numerous biological processes. This study aims to highlight the importance of vitamin B12 in nourishing hair growth and the nervous system and how its malabsorption might trigger various problems in the body. Major absorption of vitamin B12 takes place in the small intestine from several foods like milk, eggs, fish, liver, meat, and yoghurt. Several factors can cause malabsorption of vitamin B12, including atrophy of the gastric mucosa, disease of the terminal ileum in the body, and cigarette smoking. These factors can lead to the demyelination of large nerve fibers in the spinal cord, a variation in the fraction of S-adenosylmethionine to S-adenosylhomocysteine, and an alteration in TNF and epidermal growth factor (EGF) levels, which can cause optic neuropathy and hair loss. Maintaining a proper diet and leading a healthy lifestyle are crucial for maintaining vitamin B12 levels in the body, as the body can store this vitamin for up to 3–6 years. Mainly, the level of vitamin B12 in the healthy human body is 160 to 950 picogrammes per millilitre. In conclusion, the factors leading to malabsorption of vitamin B12 and their consequent deficiencies were examined. The body's numerous crucial functional pathways are influenced by vitamin B12.

Loading

Article metrics loading...

/content/journals/ijghd/10.2174/0126662906322948241211220853
2025-01-08
2025-09-26
Loading full text...

Full text loading...

References

  1. GeorgieffM.K. RamelS.E. CusickS.E. Nutritional influences on brain development.Acta Paediatr.201810781310132110.1111/apa.1428729468731
    [Google Scholar]
  2. StablerS.P. Vitamin B12.Present Knowledge in Nutrition Basic Nutrition and MetabolismAcademic Press202025727110.1016/B978‑0‑323‑66162‑1.00015‑9
    [Google Scholar]
  3. NielsenM.J. RasmussenM.R. AndersenC.B.F. NexøE. MoestrupS.K. Vitamin B12 transport from food to the body’s cells: A sophisticated, multistep pathway.Nat. Rev. Gastroenterol. Hepatol.20129634535410.1038/nrgastro.2012.7622547309
    [Google Scholar]
  4. FangH. KangJ. ZhangD. Microbial production of vitamin B12: a review and future perspectives.Microb. Cell Fact.20171611510.1186/s12934‑017‑0631‑y28137297
    [Google Scholar]
  5. ReynoldsE. Vitamin B12, folic acid, and the nervous system.Lancet Neurol.200651194996010.1016/S1474‑4422(06)70598‑117052662
    [Google Scholar]
  6. SeetharamB. AlpersD.H. Absorption and transport of cobalamin (vitamin B12).Annu. Rev. Nutr.19822134336910.1146/annurev.nu.02.070182.0020156313022
    [Google Scholar]
  7. DoscherholmenA. SwaimW.R. Impaired assimilation of egg Co 57 vitamin B 12 in patients with hypochlorhydria and achlorhydria and after gastric resection.Gastroenterology197364591391910.1016/S0016‑5085(73)80002‑24633664
    [Google Scholar]
  8. KapadiaC.R. DonaldsonR.M.Jr Disorders of cobalamin (vitamin B12) absorption and transport.Annu. Rev. Med.19853619311010.1146/annurev.me.36.020185.0005213994330
    [Google Scholar]
  9. AllenR.H. SeetharamB. PodellE. AlpersD.H. Effect of proteolytic enzymes on the binding of cobalamin to R protein and intrinsic factor. In vitro evidence that a failure to partially degrade R protein is responsible for cobalamin malabsorption in pancreatic insufficiency.J. Clin. Invest.1978611475410.1172/JCI10892422556
    [Google Scholar]
  10. OkudaK. KitazakiT. TakamatsuM. Inactivation of vitamin B12 by a binder in rat intestine and the role of intrinsic factor.Digestion197141354810.1159/0001970945554024
    [Google Scholar]
  11. Von Der LippeG. AndersenK.J. SchjönsbyH. Pancreatic extract and the intestinal uptake of vitamin B12. III. Stimulatory effect in the presence of a non-intrinsic factor vitamin B12 binder.Scand. J. Gastroenterol.197712218318710.1080/00365521.1977.1203113115312
    [Google Scholar]
  12. ToskesP.P. SmithG.W. FrancisG.M. SanderE.G. Evidence that pancreatic proteases enhance vitamin B12 absorption by acting on curde preparations of hog gastric intrinsic factor and human gastric juice.Gastroenterology1977721313610.1016/S0016‑5085(77)80299‑0318582
    [Google Scholar]
  13. HewittJ.E. GordonM.M. TaggartR.T. MohandasT.K. AlpersD.H. Human gastric intrinsic factor: Characterization of cDNA and genomic clones and localization to human chromosome 11.Genomics199110243244010.1016/0888‑7543(91)90329‑D2071148
    [Google Scholar]
  14. AlpersD.H. Russell-JonesG. Gastric intrinsic factor: The gastric and small intestinal stages of cobalamin absorption. A personal journey.Biochimie201395598999410.1016/j.biochi.2012.12.00623274574
    [Google Scholar]
  15. HallC.A. The proteins of transport of the cobalamin.Folates and Cobalamins. ZittounJ. CooperB.A. Springer-Verlag Berlin Heidelberg19895310.1007/978‑3‑642‑74364‑1_4
    [Google Scholar]
  16. TohB.H. van DrielI.R. GleesonP.A. Pernicious Anemia.N. Engl. J. Med.1997337201441144810.1056/NEJM1997111333720079358143
    [Google Scholar]
  17. HagedornC.H. AlpersD.H. Distribution of intrinsic factor-vitamin B12 receptors in human intestine.Gastroenterology19777351019102210.1016/S0016‑5085(19)31851‑7198333
    [Google Scholar]
  18. SchjønsbyH. Vitamin B12 absorption and malabsorption.Gut198930121686169110.1136/gut.30.12.16862693230
    [Google Scholar]
  19. QuadrosE.V. Advances in the understanding of cobalamin assimilation and metabolism.Br. J. Haematol.2010148219520410.1111/j.1365‑2141.2009.07937.x19832808
    [Google Scholar]
  20. DixC.J. HassanI.F. ObrayH.Y. ShahR. WilsonG. The transport of vitamin B12 through polarized monolayers of Caco-2 cells.Gastroenterology19909851272127910.1016/0016‑5085(90)90344‑Z2323519
    [Google Scholar]
  21. SchohnH. GuéantJ.L. GirrM. NexøE. BaricaultL. ZweibaumA. NicolasJ.P. Synthesis and secretion of a cobalamin-binding protein by HT 29 cell line.Biochem. J.1991280242743010.1042/bj28004271747118
    [Google Scholar]
  22. QuadrosE.V. RothenbergS.P. PanY.C. SteinS. Purification and molecular characterization of human transcobalamin II.J. Biol. Chem.198626133154551546010.1016/S0021‑9258(18)66733‑X3782074
    [Google Scholar]
  23. RothenbergS.P. QuadrosE.V. 4 Transcobalamin II and the membrane receptor for the transcobalamin II-cobalamin complex.Baillieres Clin. Haematol.19958349951410.1016/S0950‑3536(05)80218‑58534959
    [Google Scholar]
  24. ChemDraw Prime 17.1Available from : https://perkinelmer-chemdraw-prime.software.informer.com/17.1/ 2018
  25. DuttaS.K. Vitamin B12 malabsorption and omeprazole therapy.J. Am. Coll. Nutr.199413654454510.1080/07315724.1994.107184447706583
    [Google Scholar]
  26. AndrèsE. SerrajK. ZhuJ. VermorkenA.J.M. The pathophysiology of elevated vitamin B12 in clinical practice.QJM2013106650551510.1093/qjmed/hct05123447660
    [Google Scholar]
  27. GlassG.B.J. Gastric intrinsic factor and its function in the metabolism of vitamin B12.Physiol. Rev.196343452984910.1152/physrev.1963.43.4.52914056070
    [Google Scholar]
  28. KozyrakiR. FyfeJ. KristiansenM. GerdesC. JacobsenC. CuiS. ChristensenE.I. AminoffM. de la ChapelleA. KraheR. VerroustP.J. MoestrupS.K. The intrinsic factor–vitamin B12 receptor, cubilin, is a high-affinity apolipoprotein A-I receptor facilitating endocytosis of high-density lipoprotein.Nat. Med.19995665666110.1038/950410371504
    [Google Scholar]
  29. TannerS.M. AminoffM. WrightF.A. LiyanarachchiS. KuronenM. SaarinenA. MassikaO. MandelH. BrochH. de la ChapelleA. Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia.Nat. Genet.200333342642910.1038/ng109812590260
    [Google Scholar]
  30. GräsbeckR. Imerslund-Gräsbeck syndrome (selective vitamin B12 malabsorption with proteinuria).Orphanet J. Rare Dis.2006111710.1186/1750‑1172‑1‑1716722557
    [Google Scholar]
  31. AndrèsE. FothergillH. MeciliM. Efficacy of oral cobalamin (vitamin B12) therapy.Expert Opin. Pharmacother.201011224925610.1517/1465656090345605320088746
    [Google Scholar]
  32. CowenA.E. CampbellC.B. Giardiasis?A cause of vitamin B12 malabsorption.Am. J. Dig. Dis.197318538439010.1007/BF010719874573513
    [Google Scholar]
  33. SinghV.K. HauptM.E. GellerD.E. HallJ.A. DiezP.M.Q. Less common etiologies of exocrine pancreatic insufficiency.World J. Gastroenterol.201723397059707610.3748/wjg.v23.i39.705929093615
    [Google Scholar]
  34. HuddyJ.R. MachargF.M.S. LawnA.M. PrestonS.R. Exocrine pancreatic insufficiency following esophagectomy.Dis. Esophagus201326659459710.1111/dote.1200423199208
    [Google Scholar]
  35. HoltP.R. Intestinal malabsorption in the elderly.Dig. Dis.200725214415010.1159/00009947917468550
    [Google Scholar]
  36. ToskesP.P. HansellJ. CerdaJ. DerenJ.J. Vitamin B 12 malabsorption in chronic pancreatic insufficiency.N. Engl. J. Med.19712841262763210.1056/NEJM1971032528412025547614
    [Google Scholar]
  37. GiannellaR.A. BroitmanS.A. ZamcheckN. Competition between bacteria and intrinsic factor for vitamin B 12 : Implications for vitamin B 12 malabsorption in intestinal bacterial overgrowth.Gastroenterology197262225526010.1016/S0016‑5085(72)80177‑X4629318
    [Google Scholar]
  38. WelkosS.L. ToskesP.P. BaerH. SmithG.W. Importance of anaerobic bacteria in the cobalamin malabsorption of the experimental rat blind loop syndrome.Gastroenterology198180231332010.1016/0016‑5085(81)90720‑47450422
    [Google Scholar]
  39. SinghV.V. ToskesP.P. Small bowel bacterial overgrowth: Presentation, diagnosis, and treatment.Curr. Treat. Options Gastroenterol.200471192810.1007/s11938‑004‑0022‑414723835
    [Google Scholar]
  40. PagánK. HouJ. GoldenbergR.L. CliverS.P. TamuraT. Effect of smoking on serum concentrations of total homocysteine and B vitamins in mid-pregnancy.Clin. Chim. Acta20013061-210310910.1016/S0009‑8981(01)00402‑811282100
    [Google Scholar]
  41. MouhamedD.H. EzzaherA. NeffatiF. DoukiW. NajjarM.F. Effect of cigarette smoking on plasma homocysteine concentrations.cclm201149347948310.1515/CCLM.2011.06221143017
    [Google Scholar]
  42. StedmanR.L. Chemical composition of tobacco and tobacco smoke.Chem. Rev.196868215320710.1021/cr60252a0024868017
    [Google Scholar]
  43. DasturD.K. QuadrosE.V. WadiaN.H. DesaiM.M. BharuchaE.P. Effect of vegetarianism and smoking on vitamin B12, thiocyanate, and folate levels in the blood of normal subjects.BMJ19723582126026310.1136/bmj.3.5821.2605046479
    [Google Scholar]
  44. LinnellJ.C. SmithA.D. SmithC.L. WilsonJ. MatthewsD.M. Effects of smoking on metabolism and excretion of vitamin B12.BMJ19682559921521610.1136/bmj.2.5599.2155653029
    [Google Scholar]
  45. FalkH.L. Chemical agents in cigarette smoke.Compr. Physiol.2010Jun19921110.1002/cphy.cp090113
    [Google Scholar]
  46. KondoH. OsborneM.L. KolhouseJ.F. BinderM.J. PodellE.R. UtleyC.S. AbramsR.S. AllenR.H. Nitrous oxide has multiple deleterious effects on cobalamin metabolism and causes decreases in activities of both mammalian cobalamin-dependent enzymes in rats.J. Clin. Invest.19816751270128310.1172/JCI1101556112240
    [Google Scholar]
  47. FrascaV. RiazziB.S. MatthewsR.G. In vitro inactivation of methionine synthase by nitrous oxide.J. Biol. Chem.198626134158231582610.1016/S0021‑9258(18)66636‑03536916
    [Google Scholar]
  48. PiyathilakeC.J. MacalusoM. HineR.J. RichardsE.W. KrumdieckC.L. Local and systemic effects of cigarette smoking on folate and vitamin B−12.Am. J. Clin. Nutr.199460455956610.1093/ajcn/60.4.5598092091
    [Google Scholar]
  49. CarmelR. 10 malabsorption of food cobalamin.Baillieres Clin. Haematol.19958363965510.1016/S0950‑3536(05)80224‑08534965
    [Google Scholar]
  50. CaveD.R. Transmission and epidemiology of Helicobacter pylori.Am. J. Med.19961005A12S18S10.1016/S0002‑9343(96)80224‑58644777
    [Google Scholar]
  51. WeckM.N. GaoL. BrennerH. Helicobacter pylori infection and chronic atrophic gastritis: Associations according to severity of disease.Epidemiology200920456957410.1097/EDE.0b013e3181a3d5f419404195
    [Google Scholar]
  52. Veldhuyzen van ZantenS.J.O. DixonM.F. LeeA. The gastric transitional zones: Neglected links between gastroduodenal pathology and Helicobacter ecology.Gastroenterology199911651217122910.1016/S0016‑5085(99)70025‑910220514
    [Google Scholar]
  53. RaviK. JosephJ. ThomasD.M. Helicobacter pylori infection and vitamin B-12 deficiency: A cross sectional study.Asian J. Med. Sci.201784162010.3126/ajms.v8i4.17280
    [Google Scholar]
  54. DholakiaK.R. DharmarajanT.S. YadavD. OisethS. NorkusE.P. PitchumoniC.S. Vitamin B12 deficiency and gastric histopathology in older patients.World J. Gastroenterol.200511457078708310.3748/wjg.v11.i45.707816437651
    [Google Scholar]
  55. FranceschiF. AnnalisaT. TeresaD.R. GiovannaD. IaniroG. FrancoS. VivianaG. ValentinaT. RiccardoL.L. AntonioG. Role of Helicobacter pylori infection on nutrition and metabolism.World J. Gastroenterol.20142036128091281710.3748/wjg.v20.i36.1280925278679
    [Google Scholar]
  56. PetersenA.M. KrogfeltK.A. Helicobacter pylori : An invading microorganism? A review.FEMS Immunol. Med. Microbiol.200336311712610.1016/S0928‑8244(03)00020‑812738380
    [Google Scholar]
  57. KaptanK. BeyanC. UralA.U. ÇetinT. AvcuF. GülşenM. FinciR. YalçínA. Helicobacter pylori. Is it a novel causative agent in vitamin B12 deficiency?Arch. Intern. Med.200016091349135310.1001/archinte.160.9.134910809040
    [Google Scholar]
  58. LövbladK.O. RamelliG. RemondaL. NirkkoA.C. OzdobaC. SchrothG. Retardation of myelination due to dietary vitamin B12 deficiency: Cranial MRI findings.Pediatr. Radiol.199727215515810.1007/s0024700500909028851
    [Google Scholar]
  59. DrorD.K. AllenL.H. Effect of vitamin B12 deficiency on neurodevelopment in infants: Current knowledge and possible mechanisms.Nutr. Rev.200866525025510.1111/j.1753‑4887.2008.00031.x18454811
    [Google Scholar]
  60. StollhoffK. SchulteF.J. Vitamin B12 and brain development.Eur. J. Pediatr.1987146220120510.1007/BF023432373569363
    [Google Scholar]
  61. SmithA.D. WarrenM.J. RefsumH. Vitamin B12.Adv. Food Nutr. Res.20188321527910.1016/bs.afnr.2017.11.00529477223
    [Google Scholar]
  62. BaldessariniR.J. Neuropharmacology of S-adenosyl-L-methionine.Am. J. Med.19878359510310.1016/0002‑9343(87)90860‑63318448
    [Google Scholar]
  63. Grattan-SmithP.J. WilckenB. ProcopisP.G. WiseG.A. The neurological syndrome of infantile cobalamin deficiency: Developmental regression and involuntary movements.Mov. Disord.1997121394610.1002/mds.8701201088990052
    [Google Scholar]
  64. CasellaE.B. ValenteM. de NavarroJ.M. KokF. Vitamin B12 deficiency in infancy as a cause of developmental regression.Brain Dev.200527859259410.1016/j.braindev.2005.02.00516310594
    [Google Scholar]
  65. BriddonA. Homocysteine in the context of cobalamin metabolism and deficiency states.Amino Acids200324111210.1007/s00726‑002‑0319‑312624731
    [Google Scholar]
  66. MoatSJ McDowellIF Homocysteine in health and disease.200210.1093/brain/awf065
    [Google Scholar]
  67. Guerra-ShinoharaE.M. MoritaO.E. PeresS. PagliusiR.A. Sampaio NetoL.F. D’AlmeidaV. IrazustaS.P. AllenR.H. StablerS.P. Low ratio of S-adenosylmethionine to S-adenosylhomocysteine is associated with vitamin deficiency in Brazilian pregnant women and newborns.Am. J. Clin. Nutr.20048051312132110.1093/ajcn/80.5.131215531681
    [Google Scholar]
  68. ScalabrinoG. Subacute combined degeneration one century later. The neurotrophic action of cobalamin (vitamin B12) revisited.J. Neuropathol. Exp. Neurol.200160210912010.1093/jnen/60.2.10911272999
    [Google Scholar]
  69. PeracchiM. Bamonti CatenaF. PomatiM. De FranceschiM. ScalabrinoG. Human cobalamin deficiency: Alterations in serum tumour necrosis factor‐α and epidermal growth factor.Eur. J. Haematol.200167212312710.1034/j.1600‑0609.2001.t01‑1‑00507.x11722601
    [Google Scholar]
  70. ScalabrinoG. CarpoM. BamontiF. PizzinelliS. D’AvinoC. BresolinN. MeucciG. MartinelliV. ComiG.C. PeracchiM. High tumor necrosis factor‐α in levels in cerebrospinal fluid of cobalamin‐deficient patients.Ann. Neurol.200456688689010.1002/ana.2032515562428
    [Google Scholar]
  71. ScalabrinoG. PeracchiM. New insights into the pathophysiology of cobalamin deficiency.Trends Mol. Med.200612624725410.1016/j.molmed.2006.04.00816690356
    [Google Scholar]
  72. VealN. HsiehC.L. XiongS. MatoJ.M. LuS. TsukamotoH. Inhibition of lipopolysaccharide-stimulated TNF-α promoter activity by S -adenosylmethionine and 5′-methylthioadenosine.Am. J. Physiol. Gastrointest. Liver Physiol.20042872G352G36210.1152/ajpgi.00316.200315064230
    [Google Scholar]
  73. Al-ShubailiA.F. FarahS.A. HusseinJ.M. TronteljJ.V. KhuraibetA.J. Axonal and demyelinating neuropathy with reversible proximal conduction block, an unusual feature of vitamin B12 deficiency.Muscle Nerve199821101341134310.1002/(SICI)1097‑4598(199810)21:10<1341::AID‑MUS18>3.0.CO;2‑49736068
    [Google Scholar]
  74. DerinS. KoseogluS. SahinC. SahanM. Effect of vitamin B12 deficiency on olfactory function.Int Forum Allergy Rhinol.20166101051105510.1002/alr.21790
    [Google Scholar]
  75. ShyambabuC. SinhaS. TalyA.B. VijayanJ. KovoorJ.M.E. Serum vitamin B12 deficiency and hyperhomocystinemia: A reversible cause of acute chorea, cerebellar ataxia in an adult with cerebral ischemia.J. Neurol. Sci.20082731-215215410.1016/j.jns.2008.06.03418678379
    [Google Scholar]
  76. Martinez L de LetonaJ. Optic neuropathy in vitamin B12 deficiency.Lancet1998352912214710.1016/S0140‑6736(98)85055‑19672304
    [Google Scholar]
  77. ChavalaS.H. KosmorskyG.S. LeeM.K. LeeM.S. Optic neuropathy in vitamin B12 deficiency.Eur. J. Intern. Med.200516644744810.1016/j.ejim.2005.01.02116198909
    [Google Scholar]
  78. QuigleyH.A. Number of people with glaucoma worldwide.Br. J. Ophthalmol.199680538939310.1136/bjo.80.5.3898695555
    [Google Scholar]
  79. LarnerA.J. Visual failure caused by vitamin B12 deficiency optic neuropathy.Int. J. Clin. Pract.2004581097797810.1111/j.1368‑5031.2004.00306.x15587778
    [Google Scholar]
  80. PennypackerL.C. AllenR.H. KellyJ.P. MatthewsL.M. GrigsbyJ. KayeK. LindenbaumJ. StablerS.P. High prevalence of cobalamin deficiency in elderly outpatients.J. Am. Geriatr. Soc.199240121197120410.1111/j.1532‑5415.1992.tb03641.x1447433
    [Google Scholar]
  81. PiankaP. AlmogY. ManO. GoldsteinM. SelaB.A. LoewensteinA. Hyperhomocystinemia in patients with nonarteritic anterior ischemic optic neuropathy, central retinal artery occlusion, and central retinal vein occlusion.Ophthalmology200010781588159210.1016/S0161‑6420(00)00181‑010919914
    [Google Scholar]
  82. HintikkaJ. TolmunenT. TanskanenA. ViinamäkiH. High vitamin B12 level and good treatment outcome may be associated in major depressive disorder.BMC Psychiatry2003311710.1186/1471‑244X‑3‑1714641930
    [Google Scholar]
  83. DubajC. CzyżK. Furmaga-JabłońskaW. Vitamin B12 deficiency as a cause of severe neurological symptoms in breast fed infant: A case report.Ital. J. Pediatr.20204614010.1186/s13052‑020‑0804‑x31900190
    [Google Scholar]
  84. AtaF. Bint I BilalA. JavedS. Shabir ChaudhryH. SharmaR. Fatima MalikR. ChoudryH. Bhaskaran KarthaA. Optic neuropathy as a presenting feature of vitamin B-12 deficiency: A systematic review of literature and a case report.Ann. Med. Surg.20206031632210.1016/j.amsu.2020.11.01033204422
    [Google Scholar]
  85. SouzaA. MoloiM.W. Involuntary movements due to vitamin B 12 deficiency.Neurol. Res.201436121121112810.1179/1743132814Y.000000039624852503
    [Google Scholar]
  86. PatirogluT. UnalE. YildirimS. Infantile tremor syndrome associated with cobalamin therapy: A case report.Clin. Neurol. Neurosurg.201311591903190510.1016/j.clineuro.2013.05.01423764041
    [Google Scholar]
  87. O’ConnorK. GoldbergL.J. Nutrition and hair.Clin. Dermatol.202139580981810.1016/j.clindermatol.2021.05.00834785008
    [Google Scholar]
  88. GiedykM. GoliszewskaK. GrykoD. Vitamin B 12 catalysed reactions.Chem. Soc. Rev.201544113391340410.1039/C5CS00165J25945462
    [Google Scholar]
  89. AlmohannaH.M. AhmedA.A. TsatalisJ.P. TostiA. The role of vitamins and minerals in hair loss: A review.Dermatol. Ther. (Heidelb.)201991517010.1007/s13555‑018‑0278‑630547302
    [Google Scholar]
  90. AllenR.H. StablerS.P. SavageD.G. LindenbaumJ. Metabolic abnormalities in cobalamin (vitamin B 12 ) and folate deficiency.FASEB J.19937141344135310.1096/fasebj.7.14.79011047901104
    [Google Scholar]
  91. WalkerP.R. SmithB. CarsonC. LeBlancJ. SikorskaM. WoodhouseC.S. MorganA.C. Induction of apoptosis in neoplastic cells by depletion of vitamin B12.Cell Death Differ.19974323324110.1038/sj.cdd.440022516465233
    [Google Scholar]
  92. VolkovI. PressY. RudoyI. Vitamin B12 could be a “master key” in the regulation of multiple pathological processes.J. Nippon Med. Sch.2006732656910.1272/jnms.73.6516641529
    [Google Scholar]
  93. StennK.S. PausR. Controls of hair follicle cycling.Physiol. Rev.200181144949410.1152/physrev.2001.81.1.44911152763
    [Google Scholar]
  94. FathkeC. WilsonL. ShahK. KimB. HockingA. MoonR. IsikF. Wnt signaling induces epithelial differentiation during cutaneous wound healing.BMC Cell Biol.200671410.1186/1471‑2121‑7‑416426441
    [Google Scholar]
  95. EstrachS AmblerCA Lo CelsoCL HozumiK WattFM Jagged 1 is a β-catenin target gene required for ectopic hair follicle formation in adult epidermis.Development200613322442710.1242/dev.02644
    [Google Scholar]
  96. Van MaterD. KolligsF.T. DlugoszA.A. FearonE.R. Transient activation of β-catenin signaling in cutaneous keratinocytes is sufficient to trigger the active growth phase of the hair cycle in mice.Genes Dev.200317101219122410.1101/gad.107610312756226
    [Google Scholar]
  97. KruglugerW. StiefsohnK. LaciakK. MoserK. MoserC. Vitamin B12 activates the Wnt-pathway in human hair follicle cells by induction of beta-catenin and inhibition of glycogen synthase kinase-3 transcription.J. Cosmet., Dermatol. Sci. Appl201112252910.4236/jcdsa.2011.12004
    [Google Scholar]
  98. RushtonD.H. Nutritional factors and hair loss.Clin. Exp. Dermatol.200227539640410.1046/j.1365‑2230.2002.01076.x12190640
    [Google Scholar]
  99. CarmelR. Hair and fingernail changes in acquired and congenital pernicious anemia.Arch. Intern. Med.1985145348448510.1001/archinte.1985.003600301280233977516
    [Google Scholar]
  100. Yorulmaz ErtuğE. YilmazR.A. Research article reduced ferritin, folate, and vitamin B12 levels in female patients diagnosed with telogen effluvium.Int. J. Med. Biochem.20181311111410.14744/ijmb.2018.75047
    [Google Scholar]
  101. SilverP.J. DadparvarS. MaurerA.H. ParkmanH.P. Proximal and distal intragastric meal distribution during gastric emptying scintigraphy: Relationships to symptoms of gastroparesis.Neurogastroenterol. Motil.20223412e1443610.1111/nmo.1443635929769
    [Google Scholar]
  102. DurusoyC. OzenliY. AdiguzelA. BudakogluI.Y. TugalO. ArikanS. UsluA. GulecA.T. The role of psychological factors and serum zinc, folate and vitamin B 12 levels in the aetiology of trichodynia: A case-control study.Clin. Exp. Dermatol.200934778979210.1111/j.1365‑2230.2008.03165.x19508569
    [Google Scholar]
/content/journals/ijghd/10.2174/0126662906322948241211220853
Loading
/content/journals/ijghd/10.2174/0126662906322948241211220853
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test