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] Congenital adrenal hyperplasia due to 21-hydroxylase deficiency A paradigm for prenatal diagnosis and treatment
    Nimkarn, Saroj
    New, Maria I.
    SKELETAL BIOLOGY AND MEDICINE, 2010, 1192 : 5 - 11
  • [32] Future Directions in the Management of Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
    Sarafoglou, Kyriakie
    Auchus, Richard J.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2025, 110 : S74 - S87
  • [33] 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
  • [34] 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
  • [35] Update on diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    White, Perrin C.
    CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY, 2018, 25 (03) : 178 - 184
  • [36] 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
  • [37] 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
  • [38] Adult height of children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    Tsai, Meng-Ju Melody
    Tsai, Wen-Yu
    Lee, Cheng-Ting
    Liu, Shih-Yao
    Chien, Yin-Hsiu
    Tung, Yi-Ching
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2023, 122 (02) : 106 - 112
  • [39] Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
    Doerr, Helmuth G.
    Penger, Theresa
    Albrecht, Andrea
    Marx, Michaela
    Voelkl, Thomas M. K.
    JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, 2019, 11 (01) : 41 - 45
  • [40] Treatment of adult men with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    Knape, P.
    Reisch, N.
    Doerr, H.-G.
    Reincke, M.
    Quinkler, M.
    DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 2008, 133 (19) : 1025 - 1029