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In active acromegaly, IGF1 bioactivity is related to soluble Klotho levels and quality of life
The value of measuring IGF1 bioactivity in active acromegaly is unknown. Soluble Klotho (S-Klotho) level is elevated in active acromegaly and it has been suggested that S-Klotho can inhibit activation of the IGF1 receptor (IGF1R). A cross-sectional study was carried out in 15 patients with active ac...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001616/ https://www.ncbi.nlm.nih.gov/pubmed/24692508 http://dx.doi.org/10.1530/EC-14-0028 |
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author | Varewijck, A J van der Lely, A J Neggers, S J C M M Lamberts, S W J Hofland, L J Janssen, J A M J L |
author_facet | Varewijck, A J van der Lely, A J Neggers, S J C M M Lamberts, S W J Hofland, L J Janssen, J A M J L |
author_sort | Varewijck, A J |
collection | PubMed |
description | The value of measuring IGF1 bioactivity in active acromegaly is unknown. Soluble Klotho (S-Klotho) level is elevated in active acromegaly and it has been suggested that S-Klotho can inhibit activation of the IGF1 receptor (IGF1R). A cross-sectional study was carried out in 15 patients with active acromegaly based on clinical presentation, unsuppressed GH during an oral glucose tolerance test, and elevated total IGF1 levels (>+2 s.d.). Total IGF1 was measured by immunoassay, IGF1 bioactivity by the IGF1R kinase receptor activation assay and S-Klotho by an ELISA. Quality of Life (QoL) was assessed by Acromegaly QoL (AcroQoL) Questionnaire and Short-Form-36 Health Survey Questionnaire (SF-36). Out of 15 patients, nine had IGF1 bioactivity values within the reference range. S-Klotho was higher in active acromegaly compared with controls. Age-adjusted S-Klotho was significantly related to IGF1 bioactivity (r=0.75, P=0.002) and to total IGF1 (r=0.62, P=0.02). IGF1 bioactivity and total IGF1 were inversely related to the physical component summary of the SF-36 (r=−0.78, P=0.002 vs r=−0.60, P=0.03). Moreover, IGF1 bioactivity, but not total IGF1, was significantly inversely related to the physical dimension of the AcroQoL Questionnaire (r=−0.60, P=0.02 vs r=−0.37, P=0.19). In contrast to total IGF1, IGF1 bioactivity was within the reference range in a considerable number of subjects with active acromegaly. Elevated S-Klotho levels may have reduced IGF1 bioactivity. Moreover, IGF1 bioactivity was more strongly related to physical measures of QoL than total IGF1, suggesting that IGF1 bioactivity may better reflect physical limitations perceived in active acromegaly. |
format | Online Article Text |
id | pubmed-4001616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40016162014-05-09 In active acromegaly, IGF1 bioactivity is related to soluble Klotho levels and quality of life Varewijck, A J van der Lely, A J Neggers, S J C M M Lamberts, S W J Hofland, L J Janssen, J A M J L Endocr Connect Research The value of measuring IGF1 bioactivity in active acromegaly is unknown. Soluble Klotho (S-Klotho) level is elevated in active acromegaly and it has been suggested that S-Klotho can inhibit activation of the IGF1 receptor (IGF1R). A cross-sectional study was carried out in 15 patients with active acromegaly based on clinical presentation, unsuppressed GH during an oral glucose tolerance test, and elevated total IGF1 levels (>+2 s.d.). Total IGF1 was measured by immunoassay, IGF1 bioactivity by the IGF1R kinase receptor activation assay and S-Klotho by an ELISA. Quality of Life (QoL) was assessed by Acromegaly QoL (AcroQoL) Questionnaire and Short-Form-36 Health Survey Questionnaire (SF-36). Out of 15 patients, nine had IGF1 bioactivity values within the reference range. S-Klotho was higher in active acromegaly compared with controls. Age-adjusted S-Klotho was significantly related to IGF1 bioactivity (r=0.75, P=0.002) and to total IGF1 (r=0.62, P=0.02). IGF1 bioactivity and total IGF1 were inversely related to the physical component summary of the SF-36 (r=−0.78, P=0.002 vs r=−0.60, P=0.03). Moreover, IGF1 bioactivity, but not total IGF1, was significantly inversely related to the physical dimension of the AcroQoL Questionnaire (r=−0.60, P=0.02 vs r=−0.37, P=0.19). In contrast to total IGF1, IGF1 bioactivity was within the reference range in a considerable number of subjects with active acromegaly. Elevated S-Klotho levels may have reduced IGF1 bioactivity. Moreover, IGF1 bioactivity was more strongly related to physical measures of QoL than total IGF1, suggesting that IGF1 bioactivity may better reflect physical limitations perceived in active acromegaly. Bioscientifica Ltd 2014-04-15 /pmc/articles/PMC4001616/ /pubmed/24692508 http://dx.doi.org/10.1530/EC-14-0028 Text en © 2013 The authors http://creativecommons.org/licenses/by/3.0/deed.en_GB This work is licensed under a Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/deed.en_GB) |
spellingShingle | Research Varewijck, A J van der Lely, A J Neggers, S J C M M Lamberts, S W J Hofland, L J Janssen, J A M J L In active acromegaly, IGF1 bioactivity is related to soluble Klotho levels and quality of life |
title | In active acromegaly, IGF1 bioactivity is related to soluble Klotho levels and quality of life |
title_full | In active acromegaly, IGF1 bioactivity is related to soluble Klotho levels and quality of life |
title_fullStr | In active acromegaly, IGF1 bioactivity is related to soluble Klotho levels and quality of life |
title_full_unstemmed | In active acromegaly, IGF1 bioactivity is related to soluble Klotho levels and quality of life |
title_short | In active acromegaly, IGF1 bioactivity is related to soluble Klotho levels and quality of life |
title_sort | in active acromegaly, igf1 bioactivity is related to soluble klotho levels and quality of life |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001616/ https://www.ncbi.nlm.nih.gov/pubmed/24692508 http://dx.doi.org/10.1530/EC-14-0028 |
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