메뉴 건너뛰기




Volumn 95, Issue 8, 2010, Pages 3599-3604

The first case report of sulfonylurea use in a woman with permanent neonatal diabetes mellitus due to KCNJ11 mutation during a high-risk pregnancy

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA ADRENERGIC RECEPTOR BLOCKING AGENT; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CHORIONIC GONADOTROPIN; DYDROGESTERONE; GLIBENCLAMIDE; GLIPIZIDE; GLUCOSE; HEMOGLOBIN A1C; HYDROXYPROGESTERONE CAPROATE; INSULIN; INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.2; ISOPHANE INSULIN; METHYLDOPA; PREGNANCY ASSOCIATED PLASMA PROTEIN A; PROTEIN; SULFONYLUREA; THIAZIDE DIURETIC AGENT;

EID: 77955358841     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2010-0096     Document Type: Article
Times cited : (11)

References (29)
  • 1
    • 41149084500 scopus 로고    scopus 로고
    • Clinical implications of a molecular genetic classification of monogenic β-cell diabetes
    • DOI 10.1038/ncpendmet0778, PII NCPENDMET0778
    • Murphy R, Ellard S, Hattersley AT 2008 Clinical implications of a molecular genetic classification of monogenic β-cell diabetes. Nat Clin Pract Endocrinol Metab 4:200-213 (Pubitemid 351430925)
    • (2008) Nature Clinical Practice Endocrinology and Metabolism , vol.4 , Issue.4 , pp. 200-213
    • Murphy, R.1    Ellard, S.2    Hattersley, A.T.3
  • 6
    • 53849146370 scopus 로고    scopus 로고
    • Familial permanent neonatal diabetes with KCNJ11 mutation and the response to glyburide therapy - A three-year follow-up
    • Begum-Hasan J, Polychronakos C, Brill H 2008 Familial permanent neonatal diabetes with KCNJ11 mutation and the response to glyburide therapy - a three-year follow-up. J Pediatr Endocrinol Metab 21:895-903
    • (2008) J Pediatr Endocrinol Metab , vol.21 , pp. 895-903
    • Begum-Hasan, J.1    Polychronakos, C.2    Brill, H.3
  • 8
    • 20044387060 scopus 로고    scopus 로고
    • The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: Evidence for heterogeneity of beta cell function among carriers of the R201H mutation [1]
    • DOI 10.1007/s00125-005-1731-5
    • Klupa T, Edghill EL, Nazim J, Sieradzki J, Ellard S, Hattersley AT, Malecki MT 2005 The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: evidence for heterogeneity of β-cell function among carriers of the R201H mutation. Diabetologia 48:1029-1031 (Pubitemid 40767999)
    • (2005) Diabetologia , vol.48 , Issue.5 , pp. 1029-1031
    • Klupa, T.1    Edghill, E.L.2    Nazim, J.3    Sieradzki, J.4    Ellard, S.5    Hattersley, A.T.6    Malecki, M.T.7
  • 9
    • 33846008028 scopus 로고    scopus 로고
    • Transfer to sulphonylurea therapy in adult subjects with permanent neonatal diabetes due to KCNJ1-activating mutations: Evidence for improvement in insulin sensitivity
    • DOI 10.2337/dc06-1628
    • Malecki MT, Skupien J, Klupa T, Wanic K, Mlynarski W, Gach A, Solecka I, Sieradzki J 2007 Transfer to sulphonylurea therapy in adult subjects with permanent neonatal diabetes due to KCNJ11-activating mutations: evidence for improvement in insulin sensitivity. Diabetes Care 30:147-149 (Pubitemid 46052514)
    • (2007) Diabetes Care , vol.30 , Issue.1 , pp. 147-149
    • Malecki, M.T.1    Skupien, J.2    Klupa, T.3    Wanic, K.4    Mlynarski, W.5    Gach, A.6    Solecka, I.7    Sieradzki, J.8
  • 10
    • 8744262895 scopus 로고    scopus 로고
    • Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2
    • DOI 10.1210/jc.2004-1241
    • Zung A, Glaser B, Nimri R, Zadik Z 2004 Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2. J Clin Endocrinol Metab 89:5504-5507 (Pubitemid 39518433)
    • (2004) Journal of Clinical Endocrinology and Metabolism , vol.89 , Issue.11 , pp. 5504-5507
    • Zung, A.1    Glaser, B.2    Nimri, R.3    Zadik, Z.4
  • 11
    • 33646513278 scopus 로고    scopus 로고
    • Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype
    • Flanagan SE, Edghill EL, Gloyn AL, Ellard S, Hattersley AT 2006 Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype. Diabetologia 49:1190-1197
    • (2006) Diabetologia , vol.49 , pp. 1190-1197
    • Flanagan, S.E.1    Edghill, E.L.2    Gloyn, A.L.3    Ellard, S.4    Hattersley, A.T.5
  • 13
    • 33847363327 scopus 로고    scopus 로고
    • Improved motor development and good long-term glycaemic control with sulfonylurea treatment in a patient with the syndrome of intermediate developmental delay, early-onset generalised epilepsy and neonatal diabetes associated with the V59M mutation in the KCNJ11 gene
    • Slingerland AS, Nuboer R, Hadders-Algra M, Hattersley AT, Bruining GJ 2006 Improved motor development and good long-term glycaemic control with sulfonylurea treatment in a patient with the syndrome of intermediate developmental delay, early-onset generalised epilepsy and neonatal diabetes associated with the V59M mutation in the KCNJ11 gene. Diabetologia 49:2559-2563
    • (2006) Diabetologia , vol.49 , pp. 2559-2563
    • Slingerland, A.S.1    Nuboer, R.2    Hadders-Algra, M.3    Hattersley, A.T.4    Bruining, G.J.5
  • 15
    • 66449136276 scopus 로고    scopus 로고
    • Diabetic retinopathy in permanent neonatal diabetes due to Kir6.2 gene mutations: The results of a minimum 2-year follow-up after the transfer from insulin to sulphonylurea
    • Klupa T, Skupien J, Mirkiewicz-Sieradzka B, Gach A, Noczynska A, Szalecki M, Kozek E, Sieradzki J, Mlynarski W, Malecki MT 2009 Diabetic retinopathy in permanent neonatal diabetes due to Kir6.2 gene mutations: the results of a minimum 2-year follow-up after the transfer from insulin to sulphonylurea. Diabet Med 26:663-664
    • (2009) Diabet Med , vol.26 , pp. 663-664
    • Klupa, T.1    Skupien, J.2    Mirkiewicz-Sieradzka, B.3    Gach, A.4    Noczynska, A.5    Szalecki, M.6    Kozek, E.7    Sieradzki, J.8    Mlynarski, W.9    Malecki, M.T.10
  • 17
    • 0035679221 scopus 로고    scopus 로고
    • Normalization of pregnancy outcome in pregestational diabetes through functional insulin treatment and modular out-patient education adapted for pregnancy
    • DOI 10.1046/j.1464-5491.2001.00621.x
    • Howorka K, Pumprla J, Gabriel M, Feiks A, Schlusche C, Nowotny C, Schober E, Waldhoer T, Langer M 2001 Normalization of pregnancy outcome in pregestational diabetes through functional insulin treatment and modular out-patient education adapted for pregnancy. Diabet Med 18:965-972 (Pubitemid 34042932)
    • (2001) Diabetic Medicine , vol.18 , Issue.12 , pp. 965-972
    • Howorka, K.1    Pumprla, J.2    Gabriel, M.3    Feiks, A.4    Schlusche, C.5    Nowotny, C.6    Schober, E.7    Waldhoer, T.8    Langer, M.9
  • 19
    • 0022537781 scopus 로고
    • Relation of glucose tolerance to complications of pregnancy in nondiabetic women
    • Tallarigo L, Giampietro O, Penno G, Miccoli R, Gregori G, Navalesi R 1986 Relation of glucose tolerance to complications of pregnancy in nondiabetic women. N Engl J Med 315:989-992 (Pubitemid 16028579)
    • (1986) New England Journal of Medicine , vol.315 , Issue.16 , pp. 989-992
    • Tallarigo, L.1    Giampietro, O.2    Penno, G.3
  • 21
    • 0034687440 scopus 로고    scopus 로고
    • A comparison of glyburide and insulin in women with gestational diabetes mellitus
    • Langer O, Conway DL, Berkus MD, Xenakis EM, Gonzales O 2000 A comparison of glyburide and insulin in women with gestational diabetes mellitus. N Engl J Med 343:1134-1138
    • (2000) N Engl J Med , vol.343 , pp. 1134-1138
    • Langer, O.1    Conway, D.L.2    Berkus, M.D.3    Xenakis, E.M.4    Gonzales, O.5
  • 23
    • 70349653641 scopus 로고    scopus 로고
    • Effect of glucose variability on the long-term risk of microvascular complications in type 1 diabetes
    • Kilpatrick ES, Rigby AS, Atkin SL 2009 Effect of glucose variability on the long-term risk of microvascular complications in type 1 diabetes. Diabetes Care 32:1901-1903
    • (2009) Diabetes Care , vol.32 , pp. 1901-1903
    • Kilpatrick, E.S.1    Rigby, A.S.2    Atkin, S.L.3
  • 26
    • 42049119159 scopus 로고    scopus 로고
    • Safety of glyburide for gestational diabetes: A meta-analysis of pregnancy outcomes
    • Moretti ME, Rezvani M, Koren G 2008 Safety of glyburide for gestational diabetes: a meta-analysis of pregnancy outcomes. Ann Pharmacother 42:483-490
    • (2008) Ann Pharmacother , vol.42 , pp. 483-490
    • Moretti, M.E.1    Rezvani, M.2    Koren, G.3
  • 27
    • 60749104826 scopus 로고    scopus 로고
    • Benefits and risks of oral diabetes agents compared with insulin in women with gestational diabetes: A systematic review
    • Nicholson W, Bolen S, Witkop CT, Neale D, Wilson L, Bass E 2009 Benefits and risks of oral diabetes agents compared with insulin in women with gestational diabetes: a systematic review. Obstet Gynecol 113:193-205
    • (2009) Obstet Gynecol , vol.113 , pp. 193-205
    • Nicholson, W.1    Bolen, S.2    Witkop, C.T.3    Neale, D.4    Wilson, L.5    Bass, E.6
  • 28
    • 33751505489 scopus 로고    scopus 로고
    • Glucose metabolism in the late preterm infant
    • abstract ix-x
    • Garg M, Devaskar SU 2006 Glucose metabolism in the late preterm infant. Clin Perinatol 33:853-870; abstract ix-x
    • (2006) Clin Perinatol , vol.33 , pp. 853-870
    • Garg, M.1    Devaskar, S.U.2
  • 29
    • 7944238045 scopus 로고    scopus 로고
    • First prenatal diagnosis for Wolfram syndrome by molecular analysis of the WFS1 gene
    • Domènech E, Kruyer H, Gómez C, Calvo MT, Nunes V 2004 First prenatal diagnosis for Wolfram syndrome by molecular analysis of the WFS1 gene. Prenat Diagn 24:787-789
    • (2004) Prenat Diagn , vol.24 , pp. 787-789
    • Domènech, E.1    Kruyer, H.2    Gómez, C.3    Calvo, M.T.4    Nunes, V.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.