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Controlled attenuation parameter in NAFLD identifies risk of suboptimal glycaemic and metabolic control.
Patel, Preya Janubhai; Hossain, Fabrina; Horsfall, Leigh Ula; Banh, Xuan; Hayward, Kelly Lee; Williams, Suzanne; Johnson, Tracey; Brown, Nigel Neil; Saad, Nivene; Valery, Patricia Casarolli; Irvine, Katharine Margaret; Clouston, Andrew Donald; Stuart, Katherine Anne; Russell, Anthony William; Powell, Elizabeth Ellen.
Affiliation
  • Patel PJ; Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Australia; Centre for Liver Disease Research, Translational Research Institute, Faculty of Medicine and Biomedical Science, The University of Queensland, Brisbane, Australia.
  • Hossain F; Inala Primary Care, Brisbane, Australia.
  • Horsfall LU; Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Australia; Centre for Liver Disease Research, Translational Research Institute, Faculty of Medicine and Biomedical Science, The University of Queensland, Brisbane, Australia.
  • Banh X; Centre for Liver Disease Research, Translational Research Institute, Faculty of Medicine and Biomedical Science, The University of Queensland, Brisbane, Australia.
  • Hayward KL; Centre for Liver Disease Research, Translational Research Institute, Faculty of Medicine and Biomedical Science, The University of Queensland, Brisbane, Australia.
  • Williams S; Inala Primary Care, Brisbane, Australia.
  • Johnson T; Inala Primary Care, Brisbane, Australia.
  • Brown NN; Pathology Queensland, Brisbane, Australia.
  • Saad N; Department of Radiology, Princess Alexandra Hospital, Brisbane, Australia; School of Medicine, University of Queensland, Brisbane, Australia.
  • Valery PC; QIMR Berghofer Medical Research Institute, Brisbane, Australia.
  • Irvine KM; Centre for Liver Disease Research, Translational Research Institute, Faculty of Medicine and Biomedical Science, The University of Queensland, Brisbane, Australia; Mater Research, Translational Research Institute, The University of Queensland, Brisbane, Australia.
  • Clouston AD; Centre for Liver Disease Research, Translational Research Institute, Faculty of Medicine and Biomedical Science, The University of Queensland, Brisbane, Australia.
  • Stuart KA; Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Australia.
  • Russell AW; School of Medicine, University of Queensland, Brisbane, Australia; Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Brisbane, Australia.
  • Powell EE; Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Australia; Centre for Liver Disease Research, Translational Research Institute, Faculty of Medicine and Biomedical Science, The University of Queensland, Brisbane, Australia. Electronic address: e.powell@uq.edu.au.
J Diabetes Complications ; 32(8): 799-804, 2018 Aug.
Article in En | MEDLINE | ID: mdl-29861312
ABSTRACT

AIMS:

To examine the relationship between steatosis quantified by controlled attenuation parameter (CAP) values and glycaemic/metabolic control.

METHODS:

230 patients, recruited from an Endocrine clinic or primary care underwent routine Hepatology assessment, with liver stiffness measurements and simultaneous CAP. Multivariable logistic regression was performed to identify potential predictors of Metabolic Syndrome (MetS), HbA1c ≥ 7%, use of insulin, hypertriglyceridaemia and CAP ≥ 300 dB/m.

RESULTS:

Patients were 56.7 ±â€¯12.3 years of age with a high prevalence of MetS (83.5%), T2DM (81.3%), and BMI ≥ 40 kg/m2 (18%). Median CAP score was 344 dB/m, ranging from 128 to 400 dB/m. BMI (aOR 1.140 95% CI 1.068-1.216), requirement for insulin (aOR 2.599 95% CI 1.212-5.575), and serum ALT (aOR 1.018 95% CI 1.004-1.033) were independently associated with CAP ≥ 300 dB/m. Patients with CAP interquartile range < 40 (68%) had a higher median serum ALT level (p = 0.029), greater prevalence of BMI ≥ 40 kg/m2 (p = 0.020) and higher median CAP score (p < 0.001). Patients with higher CAP scores were more likely to have MetS (aOR 1.011 95% CI 1.003-1.019), HBA1c ≥ 7 (aOR 1.010 95% CI 1.003-1.016), requirement for insulin (aOR 1.007 95% CI 1.002-1.013) and hypertriglyceridemia (aOR 1.007 95% CI 1.002-1.013).

CONCLUSIONS:

Our data demonstrate that an elevated CAP reflects suboptimal metabolic control. In diabetic patients with NAFLD, CAP may be a useful point-of-care test to identify patients at risk of poorly controlled metabolic comorbidities or advanced diabetes.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycated Hemoglobin / Metabolic Syndrome / Non-alcoholic Fatty Liver Disease Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Diabetes Complications Journal subject: ENDOCRINOLOGIA Year: 2018 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycated Hemoglobin / Metabolic Syndrome / Non-alcoholic Fatty Liver Disease Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Diabetes Complications Journal subject: ENDOCRINOLOGIA Year: 2018 Document type: Article Affiliation country:
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