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Association between non-alcoholic fatty liver disease and bone turnover biomarkers in post-menopausal women with type 2 diabetes

Association between non-alcoholic fatty liver disease and bone turnover biomarkers in post-menopausal women with type 2 diabetes
Association between non-alcoholic fatty liver disease and bone turnover biomarkers in post-menopausal women with type 2 diabetes
Aim Information is lacking on the association between non-alcoholic fatty liver disease (NAFLD) and bone mineral density (BMD) or circulating bone turnover biomarkers in post-menopausal women with type 2 diabetes (T2DM). Methods We recruited 77 white post-menopausal women with T2DM, who consecutively attended our diabetes outpatient service during a 3-month period. Liver ultrasonography and transient elastography (Fibroscan®) were used for diagnosing and staging NAFLD. A dual energy X-ray absorptiometry, and serum levels of 25-hydroxyvitamin D3 [25(OH)D], parathyroid hormone and multiple bone turnover biomarkers (periostin, sclerostin, dickkopf-related protein-1 [DKK-1], C-terminal telopeptide of type 1 collagen [sCTX], procollagen type 1 N-terminal propeptide [P1NP], receptor activator of nuclear factor-kB ligand [RANKL]) were also measured. Results Overall, 10 patients had NAFLD with clinically significant fibrosis (i.e., liver stiffness measurement > 7 kPa), 52 had NAFLD without fibrosis and 15 patients were free from steatosis. Although the three patient groups had comparable values of BMD, after adjustment for age, waist circumference, HOMA-insulin resistance and serum 25(OH)D levels, patients with NAFLD and significant fibrosis had significantly higher sclerostin levels (54.1 ± 16.4 vs. 36.1 ± 11.9 vs. 42.3 ± 14.7 pmol/L) and lower levels of serum DKK-1 (26.6 ± 17.8 vs. 49.0 ± 22.4 vs. 42.9 ± 19.4 pmol/L), RANKL (0.04 ± 0.03 vs. 0.08 ± 0.06 vs. 0.11 ± 0.06 pmol/L) and sCTX (0.16 ± 0.09 vs. 0.29 ± 0.17 vs. 0.40 ± 0.28 ng/mL) compared to other groups. Serum periostin and P1NP levels did not significantly differ between the groups. Conclusion In post-menopausal women with T2DM, the presence of NAFLD and clinically significant fibrosis was strongly associated with a low bone turnover, which may reflect the presence of qualitative bone abnormalities.
1262-3636
347-355
Mantovani, Alessandro
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Sani, Elena
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Fassio, Angelo
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Colecchia, Antonio
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Viapiana, Ombretta
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Gatti, Davide
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Idolazzi, Luca
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Rossini, Maurizio
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Salvagno, Gianluca
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Lippi, Giuseppe
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Zoppini, Giacomo
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Byrne, Christopher D.
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Bonora, Enzo
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Targher, Giovanni
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Mantovani, Alessandro
19fc8a1f-60fe-403a-b70e-6b6884929e03
Sani, Elena
1acba034-45cf-4e43-b251-adc4372e64c8
Fassio, Angelo
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Colecchia, Antonio
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Viapiana, Ombretta
11574525-8fc8-48e3-a077-2b0973b08233
Gatti, Davide
cd7d29b8-1be7-456e-aaff-372e29b61e03
Idolazzi, Luca
e42b7517-6e76-4533-8da5-13d8cca220f6
Rossini, Maurizio
af626470-f2be-4ef7-8d21-9457594db653
Salvagno, Gianluca
34ab2fb7-b06c-43d7-8269-8a9769ace737
Lippi, Giuseppe
507006c0-ed97-45a4-91cc-25782dd5176c
Zoppini, Giacomo
514bd5db-7263-43a8-a379-2bdb72b9e76e
Byrne, Christopher D.
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Bonora, Enzo
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Targher, Giovanni
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Mantovani, Alessandro, Sani, Elena, Fassio, Angelo, Colecchia, Antonio, Viapiana, Ombretta, Gatti, Davide, Idolazzi, Luca, Rossini, Maurizio, Salvagno, Gianluca, Lippi, Giuseppe, Zoppini, Giacomo, Byrne, Christopher D., Bonora, Enzo and Targher, Giovanni (2019) Association between non-alcoholic fatty liver disease and bone turnover biomarkers in post-menopausal women with type 2 diabetes. Diabetes & Metabolism, 45 (4), 347-355. (doi:10.1016/j.diabet.2018.10.001).

Record type: Article

Abstract

Aim Information is lacking on the association between non-alcoholic fatty liver disease (NAFLD) and bone mineral density (BMD) or circulating bone turnover biomarkers in post-menopausal women with type 2 diabetes (T2DM). Methods We recruited 77 white post-menopausal women with T2DM, who consecutively attended our diabetes outpatient service during a 3-month period. Liver ultrasonography and transient elastography (Fibroscan®) were used for diagnosing and staging NAFLD. A dual energy X-ray absorptiometry, and serum levels of 25-hydroxyvitamin D3 [25(OH)D], parathyroid hormone and multiple bone turnover biomarkers (periostin, sclerostin, dickkopf-related protein-1 [DKK-1], C-terminal telopeptide of type 1 collagen [sCTX], procollagen type 1 N-terminal propeptide [P1NP], receptor activator of nuclear factor-kB ligand [RANKL]) were also measured. Results Overall, 10 patients had NAFLD with clinically significant fibrosis (i.e., liver stiffness measurement > 7 kPa), 52 had NAFLD without fibrosis and 15 patients were free from steatosis. Although the three patient groups had comparable values of BMD, after adjustment for age, waist circumference, HOMA-insulin resistance and serum 25(OH)D levels, patients with NAFLD and significant fibrosis had significantly higher sclerostin levels (54.1 ± 16.4 vs. 36.1 ± 11.9 vs. 42.3 ± 14.7 pmol/L) and lower levels of serum DKK-1 (26.6 ± 17.8 vs. 49.0 ± 22.4 vs. 42.9 ± 19.4 pmol/L), RANKL (0.04 ± 0.03 vs. 0.08 ± 0.06 vs. 0.11 ± 0.06 pmol/L) and sCTX (0.16 ± 0.09 vs. 0.29 ± 0.17 vs. 0.40 ± 0.28 ng/mL) compared to other groups. Serum periostin and P1NP levels did not significantly differ between the groups. Conclusion In post-menopausal women with T2DM, the presence of NAFLD and clinically significant fibrosis was strongly associated with a low bone turnover, which may reflect the presence of qualitative bone abnormalities.

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Accepted/In Press date: 2 October 2018
e-pub ahead of print date: 10 October 2018
Published date: 1 September 2019

Identifiers

Local EPrints ID: 425086
URI: http://eprints.soton.ac.uk/id/eprint/425086
ISSN: 1262-3636
PURE UUID: 1a9a589a-a3b7-48e8-8a36-6cc55f13488f
ORCID for Christopher D. Byrne: ORCID iD orcid.org/0000-0001-6322-7753

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Date deposited: 10 Oct 2018 16:30
Last modified: 16 Mar 2024 07:09

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Contributors

Author: Alessandro Mantovani
Author: Elena Sani
Author: Angelo Fassio
Author: Antonio Colecchia
Author: Ombretta Viapiana
Author: Davide Gatti
Author: Luca Idolazzi
Author: Maurizio Rossini
Author: Gianluca Salvagno
Author: Giuseppe Lippi
Author: Giacomo Zoppini
Author: Enzo Bonora
Author: Giovanni Targher

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