Endocrine
https://doi.org/10.1007/s12020-019-01998-7
RESEARCH LETTER
Sweat and vitamin D status in congenital, lifetime, untreated
GH deficiency
Cynthia S. Barros-Oliveira
1
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Roberto Salvatori
2
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Jéssica S. S. dos Santos
1
●
Paula F. C. Santos
1
●
Alécia A. Oliveira-Santos
1
●
Cindi G. Marinho
1
●
Elenilde G. Santos
1
●
Ângela C. G. B. Leal
1
●
Viviane C. Campos
1
●
Nayra P. Damascena
1
●
Carla R. P. Oliveira
1
●
Manuel H. Aguiar-Oliveira
1
Received: 22 May 2019 / Accepted: 28 June 2019
© Springer Science+Business Media, LLC, part of Springer Nature 2019
Abstract
Purpose A reciprocal relationship exists between the skin and the GH/IGF-I axis. Skin produces both IGF- I and vitamin D,
and GH and IGF-I exert several actions in the skin. Reduced sweating and altered phosphor-calcium homeostasis are
occasionally reported in subjects with GH deficiency (GHD), mostly in the setting of hypopituitarism, therefore associated to
other hormonal deficiencies. It is unclear whether these findings are due to GHD. The aim of this study was to assess skin
function in subjects with isolated GHD (IGHD) due to a mutation in the GHRH receptor gene.
Methods In a cross-sectional study we enrolled 20 IGHD and 20 local controls. Sweating (volume, conductivity and
chloride content) was assessed by a 30 min pilocarpine iontophoresis test, using the Macroduct® Sweat Collection System.
IGF-I, Insulin, PTH, 25-hydroxyvitamin D, C-reactive protein (CRP), CPK, glucose, calcium, phosphate, alkaline phos-
phatase, total proteins and fractions, urinary calcium, and insulin were measured. HOMA-IR was calculated.
Results IGHD presented lower sweating, but normal vitamin D and phosphor-calcium homeostasis. Additionally, IGHD
subjects presented lower HOMA-IR, higher CRP and reduced CPK.
Conclusion Untreated IGHD cause reduction in sweating, but does not affect phosphor-calcium homeostasis.
KeyWords GH deficiency
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skin
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sweat
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vitamin D
Introduction
Skin has many functions, some protective (against micro-
organisms, dehydration, ultraviolet light, and mechanical
damage) and other homeostatic (sweating and production of
vitamin D). A mutual influence exists between the skin and
the growth hormone/insulin growth factor I (GH/IGF-I)
axis. Skin produces IGF-I and vitamin D, and GH and IGF-I
exert several actions on the skin [1, 2]. Therefore, altera-
tions of the GH–IGF-I axis may influence sweating and the
phosphorus–calcium homeostasis.
Sweating is essential for thermoregulation, exercise
capacity, and exposure to high ambient temperatures [3].
Patients with childhood-onset GH deficiency (COGHD)
have impaired sweating ability [3]. Sweating impairment
has been also reported in men with adult-onset GHD [4].
Laron’s dwarfs, affected by GH insensitivity, also exhibit
impaired sweating ability [5].
During exposure to sunlight, ultraviolet radiation pene-
trates into the epidermis and photolyzes the synthesis of
vitamin D. A variable prevalence of vitamin D insufficiency
or deficiency has been described in patients with GHD, and
the latter was suggested to be a risk factor for vitamin D
deficiency [6–8].
We have identified in northeast Brazil a cohort of sub-
jects with severe isolated GHD (IGHD) caused by a
homozygous (c.57+1G>A) mutation in the GHRH receptor
gene (GHRHR)[9]. These individuals have normal long-
evity and quality of life and are quite active [10], coping
well with their environmental challenges, often working
outdoor under high solar exposure [11, 12]. The objectives
of this study were to evaluate sweating, vitamin D
* Roberto Salvatori
salvator@jhmi.edu
1
Division of Endocrinology, Federal University of Sergipe,
Aracaju, Sergipe 49060-100, Brazil
2
Division of Endocrinology, Diabetes and Metabolism, The Johns
Hopkins University School of Medicine, Baltimore, MD 21287,
USA
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