Vestibular function in severe GH deficiency due to an inactivating mutation in the GH-releasing hormone receptor gene

被引:3
作者
Santos-Carvalho, Hugo A. [1 ,2 ,3 ]
Aguiar-Oliveira, Manuel H. [4 ]
Salvatori, Roberto [5 ]
Valenca, Eugenia H. O. [6 ]
Andrade-Guimaraes, Alana L. [1 ,2 ,3 ]
Palanch-Repeke, Carlos E. [1 ]
Moreira-Candido, Luan P. [1 ]
Araujo-Daniel, Carlos R. [7 ]
de Oliveira-Barreto, Aline C. [1 ]
Andrade, Bruna M. R. [6 ]
Oliveira, Alaide H. A. [8 ]
Vieira, Edgar R. [9 ]
Gois-Junior, Miburge B. [1 ,2 ,3 ,7 ]
机构
[1] Univ Fed Sergipe, Ctr Hlth Sci Res, Lab Motor Control & Body Balance, BR-49060100 Sergipe, Brazil
[2] Univ Fed Sergipe, Dept Phys Therapy, Grp Estudos Atividade Fis, GREAT Grp, Sergipe, Brazil
[3] Univ Fed Sergipe, Postgrad Program Hlth Sci, Grp Estudos Atividade Fis, GREAT Grp, Sergipe, Brazil
[4] Univ Fed Sergipe, Div Endocrinol, BR-49060100 Aracaju, Sergipe, Brazil
[5] Johns Hopkins Univ, Div Endocrinol Diabet & Metab, Sch Med, Baltimore, MD 21287 USA
[6] Univ Fed Sergipe, Dept Speech & Hearing Sci, BR-49060100 Aracaju, Sergipe, Brazil
[7] Univ Fed Sergipe, Dept Stat & Actuarial Sci, Aracaju, Sergipe, Brazil
[8] Univ Fed Sergipe, Dent Div, BR-49060100 Aracaju, Sergipe, Brazil
[9] Florida Int Univ, Wertheims Coll Nursing & Hlth Sci, Dept Phys Therapy & Neurosci, Florida City, FL USA
关键词
GH deficiency; IGF-I; Vestibular function; Electronystagmography; IGF-I; GROWTH; INSULIN; LIFETIME; MATURATION; EXPRESSION; LESSONS;
D O I
10.1007/s12020-019-02178-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose Body balance involves the vestibular, visual, and proprioceptive systems. IGF-I is a GH-dependent key factor in the development and postnatal differentiation of the inner ear in mice and men, but its role in the vestibular function in adult humans is unknown. We have previously described a cohort of individuals with severe isolated GH deficiency (IGHD) caused by a mutation in the GHRH receptor (GHRHR) gene. These individuals complain of dizziness, exhibit mild sensorineural loss, but have normal postural balance, without increase in falls risk. The aim of this study was to evaluate their vestibular function. Methods We performed physical examination (clinical head impulse and Fukuda dynamic stepping test), oculomotor (saccadic eye movements, spontaneous, semi-spontaneous and opotokinetic nystagmus, and pendular tracking) and caloric stimulation (postcaloric reflex and ocular fixation index) tests, in 15 GH-naive IGHD (seven males) and 15 controls (five males). Results IGHD subjects showed lower height and weight, with similar BMI to controls, and higher number of individuals with abnormal clinical head impulse test and abnormal oculomotor tests, namely the saccadic movements and the spontaneous nystagmus. There was a nonsignificant trend in abnormalities in the Fukuda stepping test and postcaloric reflex test. Conclusions Adult untreated IGHD individuals have higher prevalence of moderate peripheral vestibular impairment, and of abnormal vestibular-ocular reflex.
引用
收藏
页码:659 / 664
页数:6
相关论文
共 33 条
  • [1] Growth Hormone Deficiency: Health and Longevity
    Aguiar-Oliveira, Manuel H.
    Bartke, Andrzej
    [J]. ENDOCRINE REVIEWS, 2019, 40 (02) : 575 - 601
  • [2] MECHANISMS IN ENDOCRINOLOGY The multiple facets of GHRH/GH/IGF-I axis: lessons from lifetime, untreated, isolated GH deficiency due to a GHRH receptor gene mutation
    Aguiar-Oliveira, Manuel H.
    Souza, Anita H. O.
    Oliveira, Carla R. P.
    Campos, Viviane C.
    Oliveira-Neto, Luiz A.
    Salvatori, Roberto
    [J]. EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2017, 177 (02) : R85 - R97
  • [3] Adult individuals with congenital, untreated, severe isolated growth hormone deficiency have satisfactory muscular function
    Andrade-Guimaraes, Alana L.
    Aguiar-Oliveira, Manuel H.
    Salvatori, Roberto
    Carvalho, Vitor O.
    Alvim-Pereira, Fabiano
    Araujo Daniel, Carlos R.
    Moreira Brasileiro, Giulliani A.
    Santana-Ribeiro, Ananda A.
    Santos-Carvalho, Hugo A.
    Oliveira, Carla R. P.
    Vieira, Edgar R.
    Gois-Junior, Miburge B.
    [J]. ENDOCRINE, 2019, 63 (01) : 112 - 119
  • [4] Cochlear hearing loss in patients with Laron syndrome
    Attias, Joseph
    Zarchi, Omer
    Nageris, Ben I.
    Laron, Zvi
    [J]. EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2012, 269 (02) : 461 - 466
  • [5] Quality of life in congenital, untreated, lifetime isolated growth hormone deficiency
    Barbosa, Jorge A. R.
    Salvatori, Roberto
    Oliveira, Carla R. P.
    Pereira, Rossana M. C.
    Farias, Catarine T.
    Britto, Allan V. de O.
    Farias, Natalia T.
    Blackford, Amanda
    Aguiar-Oliveira, Manuel H.
    [J]. PSYCHONEUROENDOCRINOLOGY, 2009, 34 (06) : 894 - 900
  • [6] Barin K., 2008, Balance function assessment and management, P229
  • [7] Sweat and vitamin D status in congenital, lifetime, untreated GH deficiency
    Barros-Oliveira, Cynthia S.
    Salvatori, Roberto
    dos Santos, Jessica S. S.
    Santos, Paula F. C.
    Oliveira-Santos, Alecia A.
    Marinho, Cindi G.
    Santos, Elenilde G.
    Leal, Angela C. G. B.
    Campos, Viviane C.
    Damascena, Nayra P.
    Oliveira, Carla R. P.
    Aguiar-Oliveira, Manuel H.
    [J]. ENDOCRINE, 2019, 65 (03) : 710 - 713
  • [8] Lessons from growth hormone receptor gene-disrupted mice: are there benefits of endocrine defects?
    Basu, Reetobrata
    Qian, Yanrong
    Kopchick, John J.
    [J]. EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2018, 178 (05) : R155 - R181
  • [9] A novel mutation in a patient with insulin-like growth factor 1 (IGF1) deficiency
    Bonapace, G
    Concolino, D
    Formicola, S
    Strisciuglio, P
    [J]. JOURNAL OF MEDICAL GENETICS, 2003, 40 (12) : 913 - 917
  • [10] BONDY CA, 1991, J NEUROSCI, V11, P3442