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Erschienen in: Der Nephrologe 4/2017

15.05.2017 | Urolithiasis | Leitthema

Hereditäre Nierenerkrankungen des Erwachsenenalters

verfasst von: M. C. Braunisch, R. Günthner, R. Satanovskij, U. Heemann

Erschienen in: Die Nephrologie | Ausgabe 4/2017

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Zusammenfassung

Die Bedeutung der Genetik in der Erwachsenennephrologie nimmt durch neue genetische Methoden ständig zu. Verschiedene hereditäre nephrologische Erkrankungen können heute relativ schnell diagnostiziert werden. Dies ermöglicht ein besseres Verständnis und ergibt Hinweise auf Therapien. In diesem Artikel werden unterschiedliche Erkrankungen der Erwachsenennephrologie, deren genetische Ursache und die durchzuführende Diagnostik erläutert. Exemplarisch dafür werden autosomal-dominante tubulointerstitielle Nierenerkrankung (ADTKD), Morbus Gaucher, Morbus Fabry, Hypophosphatasie sowie monogene Ursachen der Nephrolithiasis vorgestellt.
Literatur
1.
Zurück zum Zitat Bianchi ML (2015) Hypophosphatasia: an overview of the disease and its treatment. Osteoporos Int 26:2743–2757CrossRefPubMed Bianchi ML (2015) Hypophosphatasia: an overview of the disease and its treatment. Osteoporos Int 26:2743–2757CrossRefPubMed
2.
Zurück zum Zitat Bleyer AJ, Kmoch S, Antignac C et al (2014) Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1. Clin J Am Soc Nephrol 9:527–535CrossRefPubMedPubMedCentral Bleyer AJ, Kmoch S, Antignac C et al (2014) Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1. Clin J Am Soc Nephrol 9:527–535CrossRefPubMedPubMedCentral
3.
Zurück zum Zitat Bollee G, Dahan K, Flamant M et al (2011) Phenotype and outcome in hereditary tubulointerstitial nephritis secondary to UMOD mutations. Clin J Am Soc Nephrol 6:2429–2438CrossRefPubMedPubMedCentral Bollee G, Dahan K, Flamant M et al (2011) Phenotype and outcome in hereditary tubulointerstitial nephritis secondary to UMOD mutations. Clin J Am Soc Nephrol 6:2429–2438CrossRefPubMedPubMedCentral
4.
Zurück zum Zitat Branton MH, Schiffmann R, Sabnis SG et al (2002) Natural history of Fabry renal disease: influence of alpha-galactosidase A activity and genetic mutations on clinical course. Medicine (Baltimore) 81:122–138CrossRef Branton MH, Schiffmann R, Sabnis SG et al (2002) Natural history of Fabry renal disease: influence of alpha-galactosidase A activity and genetic mutations on clinical course. Medicine (Baltimore) 81:122–138CrossRef
5.
Zurück zum Zitat Charrow J, Andersson HC, Kaplan P et al (2000) The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease. Arch Intern Med 160:2835–2843CrossRefPubMed Charrow J, Andersson HC, Kaplan P et al (2000) The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease. Arch Intern Med 160:2835–2843CrossRefPubMed
6.
Zurück zum Zitat Eckardt KU, Alper SL, Antignac C et al (2015) Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management – A KDIGO consensus report. Kidney Int 88:676–683CrossRefPubMed Eckardt KU, Alper SL, Antignac C et al (2015) Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management – A KDIGO consensus report. Kidney Int 88:676–683CrossRefPubMed
7.
Zurück zum Zitat Ekici AB, Hackenbeck T, Moriniere V et al (2014) Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin. Kidney Int 86:589–599CrossRefPubMed Ekici AB, Hackenbeck T, Moriniere V et al (2014) Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin. Kidney Int 86:589–599CrossRefPubMed
8.
Zurück zum Zitat Faguer S, Decramer S, Chassaing N et al (2011) Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood. Kidney Int 80:768–776CrossRefPubMed Faguer S, Decramer S, Chassaing N et al (2011) Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood. Kidney Int 80:768–776CrossRefPubMed
9.
Zurück zum Zitat Ferraro PM, D’addessi A, Gambaro G (2013) When to suspect a genetic disorder in a patient with renal stones, and why. Nephrol Dial Transplant 28:811–820CrossRefPubMed Ferraro PM, D’addessi A, Gambaro G (2013) When to suspect a genetic disorder in a patient with renal stones, and why. Nephrol Dial Transplant 28:811–820CrossRefPubMed
10.
Zurück zum Zitat Gambaro G, Favaro S, D’angelo A (2001) Risk for renal failure in nephrolithiasis. Am J Kidney Dis 37:233–243CrossRefPubMed Gambaro G, Favaro S, D’angelo A (2001) Risk for renal failure in nephrolithiasis. Am J Kidney Dis 37:233–243CrossRefPubMed
11.
Zurück zum Zitat Grabowski GA, Andria G, Baldellou A et al (2004) Pediatric non-neuronopathic Gaucher disease: presentation, diagnosis and assessment. Consensus statements. Eur J Pediatr 163:58–66CrossRefPubMed Grabowski GA, Andria G, Baldellou A et al (2004) Pediatric non-neuronopathic Gaucher disease: presentation, diagnosis and assessment. Consensus statements. Eur J Pediatr 163:58–66CrossRefPubMed
12.
Zurück zum Zitat Gupta N, Oppenheim IM, Kauvar EF et al (2011) Type 2 Gaucher disease: phenotypic variation and genotypic heterogeneity. Blood Cells Mol Dis 46:75–84CrossRefPubMed Gupta N, Oppenheim IM, Kauvar EF et al (2011) Type 2 Gaucher disease: phenotypic variation and genotypic heterogeneity. Blood Cells Mol Dis 46:75–84CrossRefPubMed
13.
Zurück zum Zitat Gupta S, Ries M, Kotsopoulos S et al (2005) The relationship of vascular Glycolipid storage to clinical manifestations of Fabry disease. Medicine (Baltimore) 84:261–268CrossRef Gupta S, Ries M, Kotsopoulos S et al (2005) The relationship of vascular Glycolipid storage to clinical manifestations of Fabry disease. Medicine (Baltimore) 84:261–268CrossRef
14.
Zurück zum Zitat Halbritter J, Baum M, Hynes AM et al (2015) Fourteen monogenic genes account for 15 % of nephrolithiasis/nephrocalcinosis. J Am Soc Nephrol 26:543–551CrossRefPubMed Halbritter J, Baum M, Hynes AM et al (2015) Fourteen monogenic genes account for 15 % of nephrolithiasis/nephrocalcinosis. J Am Soc Nephrol 26:543–551CrossRefPubMed
15.
Zurück zum Zitat Kirby A, Gnirke A, Jaffe DB et al (2013) Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing. Nat Genet 45:299–303CrossRefPubMedPubMedCentral Kirby A, Gnirke A, Jaffe DB et al (2013) Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing. Nat Genet 45:299–303CrossRefPubMedPubMedCentral
16.
Zurück zum Zitat Labriola L, Olinger E, Belge H et al (2015) Paradoxical response to furosemide in uromodulin-associated kidney disease. Nephrol Dial Transplant 30:330–335CrossRefPubMed Labriola L, Olinger E, Belge H et al (2015) Paradoxical response to furosemide in uromodulin-associated kidney disease. Nephrol Dial Transplant 30:330–335CrossRefPubMed
17.
Zurück zum Zitat Mehta A, Ricci R, Widmer U et al (2004) Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry outcome survey. Eur J Clin Invest 34:236–242CrossRefPubMed Mehta A, Ricci R, Widmer U et al (2004) Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry outcome survey. Eur J Clin Invest 34:236–242CrossRefPubMed
18.
Zurück zum Zitat Meikle PJ, Hopwood JJ, Clague AE et al (1999) Prevalence of lysosomal storage disorders. JAMA 281:249–254CrossRefPubMed Meikle PJ, Hopwood JJ, Clague AE et al (1999) Prevalence of lysosomal storage disorders. JAMA 281:249–254CrossRefPubMed
20.
Zurück zum Zitat Mornet E, Nunes ME (1993) Hypophosphatasia. In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K (Hrsg) GeneReviews Hypophosphatasia. GeneReviews(R), Seattle Mornet E, Nunes ME (1993) Hypophosphatasia. In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K (Hrsg) GeneReviews Hypophosphatasia. GeneReviews(R), Seattle
21.
Zurück zum Zitat Mornet E, Yvard A, Taillandier A et al (2011) A molecular-based estimation of the prevalence of hypophosphatasia in the European population. Ann Hum Genet 75:439–445CrossRefPubMed Mornet E, Yvard A, Taillandier A et al (2011) A molecular-based estimation of the prevalence of hypophosphatasia in the European population. Ann Hum Genet 75:439–445CrossRefPubMed
23.
Zurück zum Zitat Pearle MS, Goldfarb DS, Assimos DG et al (2014) Medical management of kidney stones: AUA guideline. J Urol 192:316–324CrossRefPubMed Pearle MS, Goldfarb DS, Assimos DG et al (2014) Medical management of kidney stones: AUA guideline. J Urol 192:316–324CrossRefPubMed
24.
Zurück zum Zitat Rhodes HL, Yarram-Smith L, Rice SJ et al (2015) Clinical and genetic analysis of patients with cystinuria in the United Kingdom. Clin J Am Soc Nephrol 10:1235–1245CrossRefPubMedPubMedCentral Rhodes HL, Yarram-Smith L, Rice SJ et al (2015) Clinical and genetic analysis of patients with cystinuria in the United Kingdom. Clin J Am Soc Nephrol 10:1235–1245CrossRefPubMedPubMedCentral
25.
Zurück zum Zitat Satanovskij R, Bader A, Block M et al (2016) A new missense mutation in UMOD gene leads to severely reduced serum uromodulin concentrations – A tool for the diagnosis of uromodulin-associated kidney disease. Clin Biochem. doi:10.1016/j.clinbiochem.2016.10.003 PubMed Satanovskij R, Bader A, Block M et al (2016) A new missense mutation in UMOD gene leads to severely reduced serum uromodulin concentrations – A tool for the diagnosis of uromodulin-associated kidney disease. Clin Biochem. doi:10.​1016/​j.​clinbiochem.​2016.​10.​003 PubMed
26.
Zurück zum Zitat Schiffmann R, Hughes DA, Linthorst GE et al (2016) Screening, diagnosis, and management of patients with Fabry disease: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference. Kidney Int. doi:10.1016/j.kint.2016.10.004 PubMed Schiffmann R, Hughes DA, Linthorst GE et al (2016) Screening, diagnosis, and management of patients with Fabry disease: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference. Kidney Int. doi:10.​1016/​j.​kint.​2016.​10.​004 PubMed
27.
Zurück zum Zitat Steubl D, Block M, Herbst V et al (2016) Plasma uromodulin correlates with kidney function and identifies early stages in chronic kidney disease patients. Medicine (Baltimore) 95:e3011CrossRef Steubl D, Block M, Herbst V et al (2016) Plasma uromodulin correlates with kidney function and identifies early stages in chronic kidney disease patients. Medicine (Baltimore) 95:e3011CrossRef
28.
Metadaten
Titel
Hereditäre Nierenerkrankungen des Erwachsenenalters
verfasst von
M. C. Braunisch
R. Günthner
R. Satanovskij
U. Heemann
Publikationsdatum
15.05.2017
Verlag
Springer Medizin
Erschienen in
Die Nephrologie / Ausgabe 4/2017
Print ISSN: 2731-7463
Elektronische ISSN: 2731-7471
DOI
https://doi.org/10.1007/s11560-017-0163-9

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