메뉴 건너뛰기




Volumn 62, Issue 2, 2013, Pages 377-383

Evaluation of hypomagnesemia: Lessons from disorders of tubular transport

Author keywords

Gitelman syndrome; inherited renal disorders; Kidney; transient receptor potential melastin 6 channel (TRPM6)

Indexed keywords

CALCIUM ION; CREATININE; ELECTROLYTE; MAGNESIUM ION; MAGNESIUM OXIDE; POTASSIUM CHLORIDE; POTASSIUM ION; SODIUM CHLORIDE COTRANSPORTER;

EID: 84880622301     PISSN: 02726386     EISSN: 15236838     Source Type: Journal    
DOI: 10.1053/j.ajkd.2012.07.033     Document Type: Article
Times cited : (27)

References (46)
  • 1
    • 0033029532 scopus 로고    scopus 로고
    • Hypomagnesemia
    • Z.S. Agus Hypomagnesemia J Am Soc Nephrol 10 1999 1616 1622
    • (1999) J Am Soc Nephrol , vol.10 , pp. 1616-1622
    • Agus, Z.S.1
  • 2
    • 0031591705 scopus 로고    scopus 로고
    • [5 children with hypokalemia, hypomagnesemia and hypocalciuria (Gitelman syndrome) in one family]
    • J.J. Schweizer, J.J. van Collenburg [5 children with hypokalemia, hypomagnesemia and hypocalciuria (Gitelman syndrome) in one family] Ned Tijdschr Geneeskd 141 1997 1698 1701
    • (1997) Ned Tijdschr Geneeskd , vol.141 , pp. 1698-1701
    • Schweizer, J.J.1    Van Collenburg, J.J.2
  • 3
    • 0022510113 scopus 로고
    • Serum magnesium levels in the United States, 1971-1974
    • F.W. Lowenstein, M.F. Stanton Serum magnesium levels in the United States, 1971-1974 J Am Coll Nutr 5 1986 399 414
    • (1986) J Am Coll Nutr , vol.5 , pp. 399-414
    • Lowenstein, F.W.1    Stanton, M.F.2
  • 5
    • 0011922329 scopus 로고
    • Experimental human magnesium depletion I. Clinical observations and blood chemistry alterations
    • M.E. Shils Experimental human magnesium depletion I. Clinical observations and blood chemistry alterations Am J Clin Nutr 15 1964 133 143
    • (1964) Am J Clin Nutr , vol.15 , pp. 133-143
    • Shils, M.E.1
  • 6
    • 82755161829 scopus 로고    scopus 로고
    • Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: Novel mutations in TRPM6 and CLDN16 genes
    • T. Guran, T. Akcay, A. Bereket Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes Nephrol Dial Transplant 27 2011 667 673
    • (2011) Nephrol Dial Transplant , vol.27 , pp. 667-673
    • Guran, T.1    Akcay, T.2    Bereket, A.3
  • 7
    • 0031301943 scopus 로고    scopus 로고
    • Fractional excretion of magnesium in normal subjects and in patients with hypomagnesemia
    • M. Elisaf, K. Panteli, J. Theodorou, K.C. Siamopoulos Fractional excretion of magnesium in normal subjects and in patients with hypomagnesemia Magnes Res 10 1997 315 320
    • (1997) Magnes Res , vol.10 , pp. 315-320
    • Elisaf, M.1    Panteli, K.2    Theodorou, J.3    Siamopoulos, K.C.4
  • 8
    • 0015515015 scopus 로고
    • Evidence for parathyroid failure in magnesium deficiency
    • C.S. Anast, J.M. Mohs, S.L. Kaplan, T.W. Burns Evidence for parathyroid failure in magnesium deficiency Science 177 1972 606 608
    • (1972) Science , vol.177 , pp. 606-608
    • Anast, C.S.1    Mohs, J.M.2    Kaplan, S.L.3    Burns, T.W.4
  • 9
    • 0017183721 scopus 로고
    • Functional hypoparathyroidism and parathyroid hormone end-organ resistance in human magnesium deficiency
    • R.K. Rude, S.B. Oldham, F.R. Singer Functional hypoparathyroidism and parathyroid hormone end-organ resistance in human magnesium deficiency Clin Endocrinol (Oxf) 5 1976 209 224
    • (1976) Clin Endocrinol (Oxf) , vol.5 , pp. 209-224
    • Rude, R.K.1    Oldham, S.B.2    Singer, F.R.3
  • 10
    • 0025196297 scopus 로고
    • Frequency of hypomagnesemia and hypermagnesemia Requested vs routine
    • R. Whang, K.W. Ryder Frequency of hypomagnesemia and hypermagnesemia Requested vs routine JAMA 263 1990 3063 3064
    • (1990) JAMA , vol.263 , pp. 3063-3064
    • Whang, R.1    Ryder, K.W.2
  • 11
    • 34948878001 scopus 로고    scopus 로고
    • Mechanism of hypokalemia in magnesium deficiency
    • C.L. Huang, E. Kuo Mechanism of hypokalemia in magnesium deficiency J Am Soc Nephrol 18 2007 2649 2652
    • (2007) J Am Soc Nephrol , vol.18 , pp. 2649-2652
    • Huang, C.L.1    Kuo, E.2
  • 12
    • 78649888528 scopus 로고    scopus 로고
    • Magnesium modulates ROMK channel-mediated potassium secretion
    • L. Yang, G. Frindt, L.G. Palmer Magnesium modulates ROMK channel-mediated potassium secretion J Am Soc Nephrol 21 2010 2109 2116
    • (2010) J Am Soc Nephrol , vol.21 , pp. 2109-2116
    • Yang, L.1    Frindt, G.2    Palmer, L.G.3
  • 13
    • 80855156751 scopus 로고    scopus 로고
    • How should hypomagnesaemia be investigated and treated?
    • J. Ayuk, N.J. Gittoes How should hypomagnesaemia be investigated and treated? Clin Endocrinol (Oxf) 75 2011 743 746
    • (2011) Clin Endocrinol (Oxf) , vol.75 , pp. 743-746
    • Ayuk, J.1    Gittoes, N.J.2
  • 14
    • 0030032699 scopus 로고    scopus 로고
    • Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2
    • D.B. Simon, F.E. Karet, J.M. Hamdan, A. DiPietro, R.P. Sanjad Lifton Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2 Nat Genet 13 1996 183 188
    • (1996) Nat Genet , vol.13 , pp. 183-188
    • Simon, D.B.1    Karet, F.E.2    Hamdan, J.M.3    Dipietro, A.4    Sanjad Lifton, R.P.5
  • 16
    • 16944366243 scopus 로고    scopus 로고
    • Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
    • D.B. Simon, R.S. Bindra, T.A. Mansfield Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III Nat Genet 17 1997 171 178
    • (1997) Nat Genet , vol.17 , pp. 171-178
    • Simon, D.B.1    Bindra, R.S.2    Mansfield, T.A.3
  • 17
    • 0036707879 scopus 로고    scopus 로고
    • Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome
    • R. Vargas-Poussou, C. Huang, P. Hulin Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome J Am Soc Nephrol 13 2002 2259 2266
    • (2002) J Am Soc Nephrol , vol.13 , pp. 2259-2266
    • Vargas-Poussou, R.1    Huang, C.2    Hulin, P.3
  • 18
    • 0033763089 scopus 로고    scopus 로고
    • Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit
    • I.C. Meij, J.B. Koenderink, H. van Bokhoven Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit Nat Genet 26 2000 265 266
    • (2000) Nat Genet , vol.26 , pp. 265-266
    • Meij, I.C.1    Koenderink, J.B.2    Van Bokhoven, H.3
  • 19
    • 65649146156 scopus 로고    scopus 로고
    • HNF1B mutations associate with hypomagnesemia and renal magnesium wasting
    • S. Adalat, A.S. Woolf, K.A. Johnstone HNF1B mutations associate with hypomagnesemia and renal magnesium wasting J Am Soc Nephrol 20 2009 1123 1131
    • (2009) J Am Soc Nephrol , vol.20 , pp. 1123-1131
    • Adalat, S.1    Woolf, A.S.2    Johnstone, K.A.3
  • 20
    • 80052844338 scopus 로고    scopus 로고
    • Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood
    • S. Faguer, S. Decramer, N. Chassaing Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood Kidney Int 80 2011 768 776
    • (2011) Kidney Int , vol.80 , pp. 768-776
    • Faguer, S.1    Decramer, S.2    Chassaing, N.3
  • 21
    • 79952469460 scopus 로고    scopus 로고
    • 2+ handling, is mutated in dominant hypomagnesemia
    • 2+ handling, is mutated in dominant hypomagnesemia Am J Hum Genet 88 2011 333 343
    • (2011) Am J Hum Genet , vol.88 , pp. 333-343
    • Stuiver, M.1    Lainez, S.2    Will, C.3
  • 22
    • 65649112786 scopus 로고    scopus 로고
    • Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations
    • D. Bockenhauer, S. Feather, H.C. Stanescu Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations N Engl J Med 360 2009 1960 1970
    • (2009) N Engl J Med , vol.360 , pp. 1960-1970
    • Bockenhauer, D.1    Feather, S.2    Stanescu, H.C.3
  • 23
    • 65249156553 scopus 로고    scopus 로고
    • Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10
    • U.I. Scholl, M. Choi, T. Liu Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10 Proc Natl Acad Sci U S A 106 2009 5842 5847
    • (2009) Proc Natl Acad Sci U S A , vol.106 , pp. 5842-5847
    • Scholl, U.I.1    Choi, M.2    Liu, T.3
  • 25
    • 33751097262 scopus 로고    scopus 로고
    • Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement
    • M. Konrad, A. Schaller, D. Seelow Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement Am J Hum Genet 79 2006 949 957
    • (2006) Am J Hum Genet , vol.79 , pp. 949-957
    • Konrad, M.1    Schaller, A.2    Seelow, D.3
  • 26
    • 9044235777 scopus 로고    scopus 로고
    • Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter
    • D.B. Simon, C. Nelson-Williams, M.J. Bia Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter Nat Genet 12 1996 24 30
    • (1996) Nat Genet , vol.12 , pp. 24-30
    • Simon, D.B.1    Nelson-Williams, C.2    Bia, M.J.3
  • 27
    • 18544369466 scopus 로고    scopus 로고
    • Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family
    • K.P. Schlingmann, S. Weber, M. Peters Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family Nat Genet 31 2002 166 170
    • (2002) Nat Genet , vol.31 , pp. 166-170
    • Schlingmann, K.P.1    Weber, S.2    Peters, M.3
  • 28
    • 0036592004 scopus 로고    scopus 로고
    • Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia
    • R.Y. Walder, D. Landau, P. Meyer Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia Nat Genet 31 2002 171 174
    • (2002) Nat Genet , vol.31 , pp. 171-174
    • Walder, R.Y.1    Landau, D.2    Meyer, P.3
  • 29
    • 34547700632 scopus 로고    scopus 로고
    • Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia
    • W.M. Groenestege, S. Thebault, J. van der Wijst Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia J Clin Invest 117 2007 2260 2267
    • (2007) J Clin Invest , vol.117 , pp. 2260-2267
    • Groenestege, W.M.1    Thebault, S.2    Van Der Wijst, J.3
  • 30
    • 65249096581 scopus 로고    scopus 로고
    • A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia
    • B. Glaudemans, J. van der Wijst, R.H. Scola A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia J Clin Invest 119 2009 936 942
    • (2009) J Clin Invest , vol.119 , pp. 936-942
    • Glaudemans, B.1    Van Der Wijst, J.2    Scola, R.H.3
  • 32
    • 27944501678 scopus 로고    scopus 로고
    • Paracellin-1 and the modulation of ion selectivity of tight junctions
    • J. Hou, D.L. Paul, D.A. Goodenough Paracellin-1 and the modulation of ion selectivity of tight junctions J Cell Sci 118 2005 5109 5118
    • (2005) J Cell Sci , vol.118 , pp. 5109-5118
    • Hou, J.1    Paul, D.L.2    Goodenough, D.A.3
  • 33
    • 38849149203 scopus 로고    scopus 로고
    • Claudin-16 and claudin-19 interact and form a cation-selective tight junction complex
    • J. Hou, A. Renigunta, M. Konrad Claudin-16 and claudin-19 interact and form a cation-selective tight junction complex J Clin Invest 118 2008 619 628
    • (2008) J Clin Invest , vol.118 , pp. 619-628
    • Hou, J.1    Renigunta, A.2    Konrad, M.3
  • 34
    • 65249093634 scopus 로고    scopus 로고
    • Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome
    • K. Brochard, O. Boyer, A. Blanchard Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome Nephrol Dial Transplant 24 2009 1455 1464
    • (2009) Nephrol Dial Transplant , vol.24 , pp. 1455-1464
    • Brochard, K.1    Boyer, O.2    Blanchard, A.3
  • 35
    • 0037082531 scopus 로고    scopus 로고
    • Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies
    • M. Peters, N. Jeck, S. Reinalter Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies Am J Med 112 2002 183 190
    • (2002) Am J Med , vol.112 , pp. 183-190
    • Peters, M.1    Jeck, N.2    Reinalter, S.3
  • 36
    • 0018988982 scopus 로고
    • Intraluminal and contraluminal magnesium on magnesium and calcium transfer in the rat nephron
    • G.A. Quamme, J.H. Dirks Intraluminal and contraluminal magnesium on magnesium and calcium transfer in the rat nephron Am J Physiol 238 1980 F187 F198
    • (1980) Am J Physiol , vol.238
    • Quamme, G.A.1    Dirks, J.H.2
  • 38
    • 0033667558 scopus 로고    scopus 로고
    • Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype
    • N. Jeck, M. Konrad, M. Peters, S. Weber, K.E. Bonzel, H.W. Seyberth Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype Pediatr Res 48 2000 754 758
    • (2000) Pediatr Res , vol.48 , pp. 754-758
    • Jeck, N.1    Konrad, M.2    Peters, M.3    Weber, S.4    Bonzel, K.E.5    Seyberth, H.W.6
  • 40
    • 80255139977 scopus 로고    scopus 로고
    • The mechanism of hypocalciuria with NaCl cotransporter inhibition
    • R.F. Reilly, C.L. Huang The mechanism of hypocalciuria with NaCl cotransporter inhibition Nat Rev Nephrol 7 2011 669 674
    • (2011) Nat Rev Nephrol , vol.7 , pp. 669-674
    • Reilly, R.F.1    Huang, C.L.2
  • 41
    • 4344643606 scopus 로고    scopus 로고
    • Altered renal distal tubule structure and renal Na(+) and Ca(2+) handling in a mouse model for Gitelman's syndrome
    • J. Loffing, V. Vallon, D. Loffing-Cueni Altered renal distal tubule structure and renal Na(+) and Ca(2+) handling in a mouse model for Gitelman's syndrome J Am Soc Nephrol 15 2004 2276 2288
    • (2004) J Am Soc Nephrol , vol.15 , pp. 2276-2288
    • Loffing, J.1    Vallon, V.2    Loffing-Cueni, D.3
  • 42
    • 0029827662 scopus 로고    scopus 로고
    • Thiazide treatment of rats provokes apoptosis in distal tubule cells
    • J. Loffing, D. Loffing-Cueni, I. Hegyi Thiazide treatment of rats provokes apoptosis in distal tubule cells Kidney Int 50 1996 1180 1190
    • (1996) Kidney Int , vol.50 , pp. 1180-1190
    • Loffing, J.1    Loffing-Cueni, D.2    Hegyi, I.3
  • 43
    • 0033963206 scopus 로고    scopus 로고
    • Mammalian distal tubule: Physiology, pathophysiology, and molecular anatomy
    • R.F. Reilly, D.H. Ellison Mammalian distal tubule: physiology, pathophysiology, and molecular anatomy Physiol Rev 80 2000 277 313
    • (2000) Physiol Rev , vol.80 , pp. 277-313
    • Reilly, R.F.1    Ellison, D.H.2
  • 44
    • 0023241734 scopus 로고
    • Renal magnesium wasting in two families with autosomal dominant inheritance
    • W.B. Geven, L.A. Monnens, H.L. Willems, W.C. Buijs, B.G. ter Haar Renal magnesium wasting in two families with autosomal dominant inheritance Kidney Int 31 1987 1140 1144
    • (1987) Kidney Int , vol.31 , pp. 1140-1144
    • Geven, W.B.1    Monnens, L.A.2    Willems, H.L.3    Buijs, W.C.4    Ter Haar, B.G.5
  • 45
    • 77955640313 scopus 로고    scopus 로고
    • Effects of the EGFR inhibitor erlotinib on magnesium handling
    • H. Dimke, J. van der Wijst, T.R. Alexander Effects of the EGFR inhibitor erlotinib on magnesium handling J Am Soc Nephrol 21 2010 1309 1316
    • (2010) J Am Soc Nephrol , vol.21 , pp. 1309-1316
    • Dimke, H.1    Van Der Wijst, J.2    Alexander, T.R.3
  • 46
    • 84864477278 scopus 로고    scopus 로고
    • Magnesium in chronic kidney disease stages 3 and 4 and in dialysis patients
    • J. Cunningham, M. Rodriguez, P. Messa Magnesium in chronic kidney disease stages 3 and 4 and in dialysis patients Clin Kidney J 5 2012 i39 i51
    • (2012) Clin Kidney J , vol.5
    • Cunningham, J.1    Rodriguez, M.2    Messa, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.