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Published on: January 7, 2016
Plasma total homocysteine concentrations in adults with growth hormone (GH) deficiency: effects of GH replacement
Krzysztof C Lewandowski1, Robert D Murray, J Drzewoski
1Molecular Medicine Research Group, Biomedical Research Institute, University of Warwick, Gibbet Hill Road, Coventry, CV4 7AL, UK.
Insights
Growth hormone (GH) replacement in adults with GH deficiency did not lower total homocysteine, a cardiovascular risk factor. While IGF-1 levels increased, homocysteine levels showed no significant overall change, suggesting further research is needed for cardiovascular benefits.
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Metabolic Research
Background:
- Growth hormone (GH) deficiency is linked to higher cardiovascular risks.
- GH treatment can improve cardiovascular risk markers in GH deficient (GHD) individuals.
- Plasma total homocysteine (Hcy) is an independent cardiovascular risk factor.
Purpose of the Study:
- To investigate if GH replacement therapy reduces plasma total homocysteine (Hcy) in adult GHD patients.
- To assess the potential contribution of Hcy reduction to the cardiovascular benefits of GH replacement.
- To explore the relationship between Hcy, IGF-1, and other metabolic markers during GH treatment.
Main Methods:
- A study involving 25 adult GHD patients (17 female, 8 male, mean age 39).
- Measurements of plasma insulin, IGF-1, Hcy, FT4, creatinine, vitamin B12, and folate at baseline, 3 months, and 6 months of GH treatment.
- Statistical analysis using hierarchical models, univariate and multivariate correlation.
Main Results:
- GH treatment increased IGF-1 and insulin levels significantly.
- Plasma Hcy levels showed a transient increase at 3 months, with no significant overall change at 6 months.
- Vitamin B12 and folate levels were negatively correlated with Hcy, but IGF-1 was not.
- A small but significant increase in Hcy was observed in men at 6 months, but not in women.
Conclusions:
- Normalization of IGF-1 levels in adult GHD patients receiving GH replacement was not associated with a decrease in plasma total homocysteine.
- The impact of GH replacement on homocysteine levels and its contribution to cardiovascular prognosis in GHD requires further investigation through controlled studies.
Abstract:
Growth hormone (GH) deficiency is associated with increased cardiovascular morbidity and mortality. GH treatment improves the profile of many cardiovascular risk markers in individuals with GH deficiency (GHD). The aim of the present was to assess whether GH replacement may decrease plasma total homocysteine, an independent cardiovascular risk factor, thus potentially contributing to benefits of GH replacement in adult subjects with GHD. Twenty-five patients (17 female, 8 male), mean age 39-years, with GHD were studied. GH status had been determined by an insulin tolerance test and/or arginine stimulation test. After an overnight fast, plasma insulin, IGF-1, total homocysteine (Hcy), free thyroxine (FT4), creatinine, vitamin B12, and folate were measured at baseline (V1), 3 months (V2) and then at 6 months (V3) on GH treatment. The data were analysed by hierarchical statistical models, univariate and multivariate correlation. GH treatment resulted in an increase in IGF-1 (p<0.001, p<0.001), and insulin (p=0.068, p<0.001), at each visit, respectively. Hcy levels increased from V1 to V2 (7.7+/-0.53 to 9.15+/-0.45 micromol/L; p=0.051), but this was followed by a decline at V3 (to 8.8+/-0.59), so that the overall change of Hcy levels from V1 to V3, once individuals had achieved 'adequate' GH replacement, was no longer significantly different (p=0.090). When separated by gender, at 6 months (V3) there was a small, but significant increase in Hcy in men (p=0.028), but not in women (p=0.58). There was no significant change in B12, folate, free T4 or creatinine levels. Univariate analysis revealed that only B12 and folate showed significant negative relationships with Hcy (B12: parameter= -0.013, p<0.001; folate: parameter=-1.31, p<0.001), but not between Hcy and IGF-1 (p=0.18). In a multiple variable model, both B12 and folate remained significantly negatively associated with plasma total homocysteine (p=0.018; p<0.001, respectively). In this observational study normalisation of IGF-1 levels in adult subjects with growth hormone deficiency was not associated with a fall in total homocysteine. Before firm conclusions can be drawn about the contribution of changes in plasma homocysteine concentrations to cardiovascular prognosis in adult GHD patients receiving GH replacement, further controlled studies are required.
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