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
  • [31] GUIDELINES FOR TREATMENT OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
    Dumic, Miroslav
    PAEDIATRIA CROATICA, 2012, 56 : 31 - 32
  • [32] Growth and pubertal characteristics in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    Trinh, Lien
    Nimkarn, Saroj
    New, Maria I.
    Lin-Su, Karen
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2007, 20 (08): : 883 - 891
  • [33] Steroid 21 Hydroxylase Deficiency Congenital Adrenal Hyperplasia
    Nimkarn, Saroj
    Lin-Su, Karen
    New, Maria I.
    ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 2009, 38 (04) : 699 - +
  • [34] Steroid 21 Hydroxylase Deficiency Congenital Adrenal Hyperplasia
    Nimkarn, Saroj
    Lin-Su, Karen
    New, Maria I.
    PEDIATRIC CLINICS OF NORTH AMERICA, 2011, 58 (05) : 1281 - +
  • [35] 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia
    Shaw, Amy M.
    NEONATAL NETWORK, 2010, 29 (03): : 191 - 196
  • [36] Antenatal Diagnosis and Treatment in Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency and Congenital Adrenal Hyperplasia Screening in Newborns
    Abali, Zehra Yavas
    Kurnaz, Erdal
    Guran, Tulay
    JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, 2025, 17 : 33 - 43
  • [37] Genetic Characterization of a Cohort of Italian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
    Paola Concolino
    Alessia Perrucci
    Cinzia Carrozza
    Andrea Urbani
    Molecular Diagnosis & Therapy, 2023, 27 : 621 - 630
  • [38] Cortical bone mineral density in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    El-Maouche, Diala
    Collier, Suzanne
    Prasad, Mala
    Reynolds, James C.
    Merke, Deborah P.
    CLINICAL ENDOCRINOLOGY, 2015, 82 (03) : 330 - 337
  • [39] BLUNTED ADRENARCHE IN PATIENTS WITH CLASSICAL CONGENITAL ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
    SELLERS, EP
    MACGILLIVRAY, MH
    ENDOCRINE RESEARCH, 1995, 21 (03) : 537 - 544
  • [40] Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency
    Mnif, Mouna Feki
    Kamoun, Mahdi
    Mnif, Fatma
    Charfi, Nadia
    Kallel, Nozha
    Ben Naceur, Basma
    Rekik, Nabila
    Mnif, Zainab
    Sfar, Mohamed Habib
    Sfar, Mohamed Tahar
    Hachicha, Mongia
    Keskes, Leila Ammar
    Abid, Mohamed
    AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2012, 344 (05): : 363 - 373