Cardiac function in paediatric patients with congenital adrenal hyperplasia due to 21 hydroxylase deficiency

被引:10
|
作者
Mooij, Christiaan F. [1 ]
Pourier, Milanthy S. [2 ]
Weijers, Gert [3 ]
de Korte, Chris L. [3 ]
Fejzic, Zina [4 ]
Claahsen-van der Grinten, Hedi L. [1 ]
Kapusta, Livia [4 ,5 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Amalia Childrens Hosp, Div Pediat Endocrinol,Dept Pediat, Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Amalia Childrens Hosp, Dept Pediat, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Radiol, Med Ultrasound Imaging Ctr, Nijmegen, Netherlands
[4] Radboud Univ Nijmegen, Med Ctr, Amalia Childrens Hosp, Childrens Heart Ctr, Nijmegen, Netherlands
[5] Tel Aviv Univ, Sackler Sch Med, Tel Aviv Sourasky Med Ctr, Pediat Cardiol Unit, Tel Aviv, Israel
关键词
cardiac function; cardiovascular risk; congenital adrenal hyperplasia; echocardiography; SPECKLE TRACKING ECHOCARDIOGRAPHY; VENTRICULAR DIASTOLIC FUNCTION; SYSTOLIC WALL STRESS; CUSHINGS-SYNDROME; 21-HYDROXYLASE DEFICIENCY; EJECTION FRACTION; LV DYSFUNCTION; CHILDREN; POPULATION; HEALTH;
D O I
10.1111/cen.13529
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundHyperandrogenism and exogenous glucocorticoid excess may cause unfavourable changes in the cardiovascular risk profile of patients with congenital adrenal hyperplasia (CAH). ObjectiveTo evaluate the cardiac function in paediatric patients with CAH. Patients and methodsTwenty-seven paediatric patients with CAH, aged 8-16years, were evaluated by physical examination, electrocardiogram (ECG), conventional echocardiography, tissue Doppler imaging and two-dimensional (2D) myocardial strain (rate) imaging. Results were compared to 27 age- and gender- matched healthy controls. ResultsNo signs of left ventricular hypertrophy or dilatation were detected on echocardiography. ECG revealed a high prevalence (25.9%) of incomplete right bundle branch block. Left ventricular posterior wall thickness in diastole (LVPWd) was significantly lower in patients with CAH compared to controls (5.55 vs 6.53mm; P=.009). The LVPWd Z-score was significantly lower in patients with CAH yet within the normal range (-1.12 vs -0.35; P=.002). Isovolumetric relaxation time was significantly lower in patients with CAH (49 vs 62ms; P=.003). Global longitudinal, radial and circumferential strain was not significantly different compared to controls. Global radial strain rate was significantly higher compared to healthy controls (2.58 vs 2.06 1/s; P=.046). Global longitudinal strain was negatively correlated with 24-hour blood pressure parameters. ConclusionCardiac evaluation of paediatric patients with CAH showed no signs of left ventricular hypertrophy or ventricular dilatation. LVPWd was lower in patients with CAH than in controls but within the normal range. A shorter isovolumetric relaxation time in patients with CAH may be a sign of mild left ventricular diastolic dysfunction.
引用
收藏
页码:364 / 371
页数:8
相关论文
共 50 条
  • [41] Genetic Characterization of a Cohort of Italian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
    Concolino, Paola
    Perrucci, Alessia
    Carrozza, Cinzia
    Urbani, Andrea
    MOLECULAR DIAGNOSIS & THERAPY, 2023, 27 (05) : 621 - 630
  • [42] Fertility outcome in male and female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    Kamoun, Mahdi
    Mnif, Mouna
    Charfi, Nadia
    Naceur, Basma
    Mnif, Fatma
    Rekik, Nabila
    Mnif, Zainab
    Sfar, Mohamed
    Sfar, Mohamed
    Hachicha, Mongia
    Salem, Azza
    Keskes, Leila
    Abid, Mohamed
    MIDDLE EAST FERTILITY SOCIETY JOURNAL, 2014, 19 (02) : 89 - 95
  • [43] AROMATASE INHIBITOR INCREASES THE HEIGHT OF PATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
    Xi, Wang
    Mao, Jangfeng
    Li, Shuying
    Zhao, Yaling
    Nie, Min
    Yu, Bingqing
    Gao, Yinjie
    Lu, Lin
    Wu, Xueyan
    ENDOCRINE PRACTICE, 2020, 26 (09) : 997 - 1002
  • [44] Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    Bachelot, Anne
    Plu-Bureau, Genevieve
    Thibaud, Elisabeth
    Laborde, Kathleen
    Pinto, Graziella
    Samara, Dinane
    Nihoul-Fekete, Claire
    Kuttenn, Frederique
    Polak, Michel
    Touraine, Philippe
    HORMONE RESEARCH, 2007, 67 (06) : 268 - 276
  • [45] Mutational characterization of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Malaysia
    Balraj, P.
    Lim, P. G.
    Sidek, H.
    Wu, L. L.
    Khoo, A. S. B.
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2013, 36 (06) : 366 - 374
  • [46] Congenital adrenal hyperplasia due to 21-hydroxylase deficiency associated with bilateral keratoconus
    Incorvaia, C
    Parmeggiani, F
    Costagliola, C
    Perri, P
    Tittoni, M
    Sebastiani, A
    AMERICAN JOURNAL OF OPHTHALMOLOGY, 2003, 135 (04) : 557 - 559
  • [47] A Rare Combination: Congenital Adrenal Hyperplasia Due To 21 Hydroxylase Deficiency and Turner Syndrome
    Kendirci, Havva Nur Peltek
    Aycan, Zehra
    Cetinkaya, Semra
    Bas, Veysel Nijat
    Agladioglu, Sebahat Yilmaz
    Onder, Asan
    JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, 2012, 4 (04) : 213 - 215
  • [48] Barriers to the Management of Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
    Eitel, Kelsey B.
    Fechner, Patricia Y.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2025, 110 : S67 - S73
  • [49] Procedure for neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    Honour, JW
    Torresani, T
    Toublanc, JE
    Larsson, A
    Grueters-Kieslich, A
    Giovanelli, G
    Donaldson, M
    Ferrandez-Longas, A
    Klett, M
    Hnikova, O
    Schrama, SMPFDK
    HORMONE RESEARCH, 2001, 55 (04) : 201 - 205
  • [50] Genetics in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and Clinical Implications
    Concolino, Paola
    Falhammar, Henrik
    JOURNAL OF THE ENDOCRINE SOCIETY, 2025, 9 (03)