Cardiac dysfunction in children with mulibrey nanism

被引:15
|
作者
Eerola, A. [1 ]
Pihkala, J. I.
Karlberg, N.
Lipsanen-Nyman, M.
Jokinen, E.
机构
[1] Univ Helsinki, Hosp Children & Adolescents, Dept Pediat Cardiol, FIN-00029 Helsinki, Finland
[2] Kuopio Univ Hosp, Dept Pediat, SF-70210 Kuopio, Finland
[3] Univ Helsinki, Hosp Children & Adolescents, Dept Pediat Endocrinol, FIN-00029 Helsinki, Finland
关键词
Mulibrey nanism; Echocardiography; natriuretic peptides;
D O I
10.1007/s00246-006-0007-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mulibrey nanism is an autosomal recessive disease with severe growth failure and multiple organ involvement. Heart manifestations include constrictive pericarditis and restrictive cardiomyopathy. The purpose of this study was to evaluate left ventricular (LV) diastolic and systolic function in children with mulibrey nanism utilizing two- and three- dimensional (2-D and 3-D) echocardiography and measurement of serum levels of natriuretic peptides. Of the 30 children diagnosed with mulibrey nanism in Finland, 26 participated. The control group comprised 26 children. In 2-D echocardiography, the interventricular septum and LV posterior wall were thicker in patients. The left atrium/aorta ratio measured a median 1.8 (range, 1.4-2.5) in patients and 1.3 (range, 1.0-1.7) in controls (p < 0.001). Patients differed from controls in several indices of diastolic LV function. In 3-D echocardiography, LV end diastolic volume measured a median of 51.9 ml/m(2) (range, 33.3-73.4) in patients and 59.7 ml/m(2) (range, 37.6-87.6) in controls (p = 0.040), and serum levels of N-terminal proatriopeptide and N-terminal pro-brain natriuretic peptide measured, respectively, a median of 0.54 nmol/L (range, 0.04-4.7) and 289 ng/L (range, 18-9170) in patients and 0.28 nmol/L (range, 0.09-0.72; p < 0.001) and 54 ng/L (range, 26-139; p < 0.001) in controls. They correlated with several indices of diastolic LV function. In a significant proportion of children with mulibrey nanism, myocardial function is impaired. Significant correlations appeared between indices of LV function, size of the left atrium, and levels of natriuretic peptides, showing that measurement of serum levels of natriuretic peptides is a useful follow-up method despite its dependence on loading conditions.
引用
收藏
页码:155 / 162
页数:8
相关论文
共 50 条
  • [11] MULIBREY NANISM - 3 ADDITIONAL PATIENTS AND A REVIEW OF 39 PATIENTS
    LAPUNZINA, P
    RODRIGUEZ, JI
    DEMATTEO, E
    GRACIA, R
    MORENO, F
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 55 (03): : 349 - 355
  • [12] Wilms tumor with Mulibrey Nanism: A case report and review of literature
    Upasana, Karthik
    Thakkar, Dhwanee
    Gautam, Dheeraj
    Sachdev, Manvinder Singh
    Yadav, Anjali
    Kapoor, Rohit
    Raghunathan, Veena
    Dhaliwal, Maninder Singh
    Bhargava, Kartikeya
    Nair, Sandhya
    Sharma, Jaiprakash
    Rastogi, Neha
    Yadav, Satya Prakash
    CANCER REPORTS, 2022, 5 (05)
  • [13] New intragenic rearrangements in non-Finnish mulibrey nanism
    Jobic, Florence
    Morin, Gilles
    Vincent-Delorme, Catherine
    Cadet, Estelle
    Cabry, Rosalie
    Mathieu-Dramard, Michele
    Copin, Henri
    Rochette, Jacques
    Jedraszak, Guillaume
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (10) : 2782 - 2788
  • [14] Assessment of mulibrey nanism cardiopathy with functional magnetic resonance imaging
    Kokki, S.
    Lauerma, K.
    Kupari, M.
    Lipsanen-Nyman, M.
    Hekali, P.
    MAGNETIC RESONANCE MATERIALS IN PHYSICS BIOLOGY AND MEDICINE, 2000, 11 (01) : 84 - 86
  • [15] Skeletal Phenotype in Mulibrey Nanism, A Monogenic Skeletal Dysplasia With Fibrous Dysplasia
    Karlberg, Susann
    Toiviainen-Salo, Sanna
    Lipsanen-Nyman, Marita
    Makitie, Outi
    CLINICAL GENETICS, 2025, 107 (03) : 271 - 277
  • [16] A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy
    Doganci, Tumay
    Konuk, Berrin E. Yuksel
    Alpan, Nursel
    Konuk, Onur
    Hamalainen, Riikka H.
    Lehesjoki, Anna-Elina
    Tekin, Mustafa
    CLINICAL DYSMORPHOLOGY, 2007, 16 (03) : 173 - 176
  • [17] ANTIBODY DEFICIENCY AND ISOLATED GROWTH-HORMONE DEFICIENCY IN A GIRL WITH MULIBREY NANISM
    HARALDSSON, A
    VANDERBURGT, CJAM
    WEEMAES, CMR
    OTTEN, B
    BAKKEREN, JAJM
    STOELINGA, GBA
    EUROPEAN JOURNAL OF PEDIATRICS, 1993, 152 (06) : 509 - 512
  • [18] Premature ovarian insufficiency and early depletion of the ovarian reserve in the monogenic Mulibrey nanism disorder
    Karlberg, Susann
    Tiitinen, Aila
    Alfthan, Henrik
    Lipsanen-Nyman, Marita
    HUMAN REPRODUCTION, 2018, 33 (07) : 1254 - 1261
  • [19] Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing
    Mozzillo, Enza
    Cozzolino, Carla
    Genesio, Rita
    Melis, Daniela
    Frisso, Giulia
    Orrico, Ada
    Lombardo, Barbara
    Fattorusso, Valentina
    Discepolo, Valentina
    Della Casa, Roberto
    Simonelli, Francesca
    Nitsch, Lucio
    Salvatore, Francesco
    Franzese, Adriana
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2016, 170 (08) : 2196 - 2199
  • [20] Mulibrey Nanism and the Real Time Use of Genome and Biobank Engines to Inform Clinical Care in an Ultrarare Disease
    Weldy, Chad S.
    Ashley, Euan A.
    CIRCULATION-GENOMIC AND PRECISION MEDICINE, 2021, 14 (03): : 387 - 389