Childhood hypertension in autosomal-dominant hypertension with brachydactyly

Hypertension

Volumn 56, Issue 5, 2010, Pages 988-994

  Toka, Okan ^a   Maass, Philipp G ^b   Aydin, Atakan ^b   Toka, Hakan ^b,c   Hübner, Norbert ^b   Rüschendorf, Franz ^b   Gong, Maolian ^b   Luft, Friedrich C ^b   Bähring, Sylvia ^b  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^c BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

adolescent hypertension; autosomal dominant hypertension with brachydactyly; childhood hypertension; genetic hypertension; prepubertal growth spurt

Indexed keywords

ANTIHYPERTENSIVE AGENT;

ADOLESCENT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT DISORDER HYPERTENSION WITH BRACHYDACTYLY; AUTOSOMAL DOMINANT HYPERTENSION WITH BRACHYDACTYLY; BLOOD PRESSURE MEASUREMENT; BRACHYDACTYLY; CHILD; CHILDHOOD DISEASE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DRUG EFFICACY; FEMALE; GENE REARRANGEMENT; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENOTYPE; GROUPS BY AGE; GROWTH ACCELERATION; HUMAN; HYPERTENSION; INFANT; MALE; ONSET AGE; PHENOTYPE; PREPUBERTY; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SHORT STATURE; SINGLE NUCLEOTIDE POLYMORPHISM; TODDLER; BODY HEIGHT; GENETICS; LIMB MALFORMATION; PUBERTY;

ADOLESCENT; BODY HEIGHT; CHILD; CHILD, PRESCHOOL; FEMALE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; HYPERTENSION; INFANT; LIMB DEFORMITIES, CONGENITAL; LINKAGE (GENETICS); MALE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PUBERTY;

EID: 78149238595     PISSN: 0194911X     EISSN: None     Source Type: Journal    
DOI: 10.1161/HYPERTENSIONAHA.110.156620     Document Type: Article

References (30)

1. Bilginturan N, Zileli S, Karacadag S, Pirnar T. Hereditary brachydactyly associated with hypertension. J Med Genet. 1973;10:253-259.
2. Bahring S, Kann M, Neuenfeld Y, Gong M, Chitayat D, Toka HR, Toka O, Plessis G, Maass P, Rauch A, Aydin A, Luft FC. Inversion region for hypertension and brachydactyly on chromosome 12p features multiple splicing and noncoding RNA. Hypertension. 2008;51:426-431.
3. Bahring S, Rauch A, Toka O, Schroeder C, Hesse C, Siedler H, Fesus G, Haefeli WE, Busjahn A, Aydin A, Neuenfeld Y, Muhl A, Toka HR, Gollasch M, Jordan J, Luft FC. Autosomal-dominant hypertension with type E brachydactyly is caused by rearrangement on the short arm of chromosome 12. Hypertension. 2004;43:471-476.
4. Jordan J, Toka HR, Heusser K, Toka O, Shannon JR, Tank J, Diedrich A, Stabroth C, Stoffels M, Naraghi R, Oelkers W, Schuster H, Schobel HP, Haller H, Luft FC. Severely impaired baroreflex-buffering in patients with monogenic hypertension and neurovascular contact. Circulation. 2000;102:2611-2618.
5. Schuster H, Toka O, Toka HR, Busjahn A, Oztekin O, Wienker TF, Bilginturan N, Bahring S, Skrabal F, Haller H, Luft FC. A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly. Kidney Int. 1998;53:167-172.
6. Schuster H, Wienker TE, Bahring S, Bilginturan N, Toka HR, Neitzel H, Jeschke E, Toka O, Gilbert D, Lowe A, Ott J, Haller H, Luft FC. Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12. Nat Genet. 1996;13:98-100. (Pubitemid 126528236)
7. Schuster H, Wienker TF, Toka HR, Bahring S, Jeschke E, Toka O, Busjahn A, Hempel A, Tahlhammer C, Oelkers W, Kunze J, Bilginturan N, Haller H, Luft FC. Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertension. Hypertension. 1996;28:1085-1092. (Pubitemid 26415829)
8. Toka HR, Bahring S, Chitayat D, Melby JC, Whitehead R, Jeschke E, Wienker TF, Toka O, Schuster H, Luft FC. Families with autosomal dominant brachydactyly type E, short stature, and severe hypertension. Ann Intern Med. 1998;129:204-208.
9. Ji W, Foo JN, O'Roak BJ, Zhao H, Larson MG, Simon DB, Newton-Cheh C, State MW, Levy D, Lifton RP. Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nat Genet. 2008;40:592-599.
10. Harrison M, Maresso K, Broeckel U. Genetic determinants of hypertension: an update. Curr Hypertens Rep. 2008;10:488-495.
11. Lifton RP, Dluhy RG, Powers M, Rich GM, Cook S, Ulick S, Lalouel JM. A chimaeric 11 β-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension. Nature. 1992;355:262-265.
12. Lifton RP, Gharavi AG, Geller DS. Molecular mechanisms of human hypertension. Cell. 2001;104:545-556.
13. Mein CA, Caulfield MJ, Munroe PB. Selection of candidate genes in hypertension. Methods Mol Med. 2005;108:107-129.
14. Binder A. A review of the genetics of essential hypertension. Curr Opin Cardiol. 2007;22:176-184.
15. Quack I, Vonend O, Rump LC. Familial hyperaldosteronism I-III. Horm Metab Res. 2010;42:424-428.
16. Luft FC. Mendelian forms of human hypertension and mechanisms of disease. Clin Med Res. 2003;1:291-300.
17. Gong M, Zhang H, Schulz H, Lee YA, Sun K, Bahring S, Luft FC, Nurnberg P, Reis A, Rohde K, Ganten D, Hui R, Hubner N. Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p. HumMol Genet. 2003;12:1273-1277.
18. Harrap SB, Cui JS, Wong ZY, Hopper JL. Familial and genomic analyses of postural changes in systolic and diastolic blood pressure. Hypertension. 2004;43:586-591.
19. Tank J, Toka O, Toka HR, Jordan J, Diedrich A, Busjahn A, Luft FC. Autonomic nervous system function in patients with monogenic hypertension and brachydactyly: a field study in north-eastern Turkey. J Hum Hypertens. 2001;15:787-792.
20. Naraghi R, Schuster H, Toka HR, Bahring S, Toka O, Oztekin O, Bilginturan N, Knoblauch H, Wienker TF, Busjahn A, Haller H, Fahlbusch R, Luft FC. Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly. Stroke. 1997;28:1749-1754. (Pubitemid 27391444)
21. Ruschendorf F, Nurnberg P. ALOHOMORA: a tool for linkage analysis using 10K SNP array data. Bioinformatics. 2005;21:2123-2125.
22. Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet. 2002;30:97-101.
23. Telatar B, Comert S, Vitrinel A, Erginoz E. Anthropometric measurements of term neonates from a state hospital in Turkey. East Mediterr Health J. 2009;15:1412-1419.
24. Hatipoglu N, Kurtoglu S, Oztürk A, Mazicioglu M. The weight and height percentiles in 6-18 years old children in Kayseri and comparison with Isthanbul data. J Clin Res Ped Endo 2009. 2009;1:129-135.
25. World Health Organization. WHO/Programmes and Projects/Child Growth Standards. Available at: http://www.who.int/childgrowth/standards/en/. Accessed September 3, 2010.
26. Poznanski AK, Werder EA, Giedion A, Martin A, Shaw H. The pattern of shortening of the bones of the hand in PHP and PPHP: a comparison with brachydactyly E, Turner Syndrome, and acrodysostosis. Radiology. 1977;123:707-718.
27. National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents. The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents. Pediatrics. 2004;114:555-576.
28. McKusick VA, O'Neil MJF. Online Mendelian Inheritance in Men, Johns Hopkins University 1966-2010, edition 4/26/2010, MIN# 113300, Brachydactyly, Type E1; BDE1. Available at http://www.ncbi.nlm.nih. gov/omim/113300. Accessed September 3, 2010.
29. Mancia G, De Backer G, Dominiczak A, Cifkova R, Fagard R, Germano G, Grassi G, Heagerty AM, Kjeldsen SE, Laurent S, Narkiewicz K, Ruilope L, Rynkiewicz A, Schmieder RE, Boudier HA, Zanchetti A, Vahanian A, Camm J, De Caterina R, Dean V, Dickstein K, Filippatos G, Funck-Brentano C, Hellemans I, Kristensen SD, McGregor K, Sechtem U, Silber S, Tendera M, Widimsky P, Zamorano JL, Erdine S, Kiowski W, Agabiti-Rosei E, Ambrosioni E, Lindholm LH, Viigimaa M, Adamopoulos S, Bertomeu V, Clement D, Farsang C, Gaita D, Lip G, Mallion JM, Manolis AJ, Nilsson PM, O'Brien E, Ponikowski P, Redon J, Ruschitzka F, Tamargo J, van Zwieten P, Waeber B, Williams B. 2007 guidelines for the management of arterial hypertension: the Task Force for the Management of Arterial Hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC). J Hypertens. 2007;25:1105-1187. (Pubitemid 46924065)
30. Jones DW, Hall JE. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure and evidence from new hypertension trials. Hypertension. 2004;43:1-3.