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Long-Term Adverse Effect of Liver Stiffness on Glycaemic Control in Type 2 Diabetic Patients with Nonalcoholic Fatty Liver Disease: A Pilot Study
被引:11
|作者:
Mantovani, Alessandro
[1
]
Taverna, Antonio
[1
]
Cappelli, Davide
[1
]
Beatrice, Giorgia
[1
]
Csermely, Alessandro
[1
]
Sani, Elena
[1
]
Byrne, Christopher D.
[2
,3
,4
,5
]
Targher, Giovanni
[1
]
机构:
[1] Univ Verona, Dept Med, Sect Endocrinol Diabet & Metab, I-37126 Verona, Italy
[2] Univ Southampton, Fac Med, Nutr & Metab, Southampton SO17 1BJ, Hants, England
[3] Southampton Gen Hosp, Southampton Natl Inst Hlth, Tremona Rd, Southampton SO16 6YD, Hants, England
[4] Southampton Gen Hosp, Care Res Biomed Res Ctr, Tremona Rd, Southampton SO16 6YD, Hants, England
[5] Univ Hosp Southampton, Southampton Gen Hosp, Tremona Rd, Southampton SO16 6YD, Hants, England
关键词:
nonalcoholic fatty liver disease;
NAFLD;
MAFLD;
metabolic associated fatty liver disease;
type;
2;
diabetes;
T2DM;
fibrosis;
liver stiffness;
RATHER;
D O I:
10.3390/ijms232012481
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Currently, there are limited data regarding the long-term effect of liver stiffness on glycaemic control in patients with type 2 diabetes mellitus (T2DM) and nonalcoholic fatty liver disease (NAFLD). We prospectively followed an outpatient sample of 61 consecutive postmenopausal women with T2DM and NAFLD who had baseline data on liver ultrasonography and Fibroscan (R) -assessed liver stiffness measurement (LSM) in 2017 and who underwent follow-up in 2022. Haemoglobin A1c (HbA1c) was measured both at baseline and follow-up. At baseline, 52 patients had NAFLD (hepatic steatosis) alone, and 9 had NAFLD with coexisting clinically significant fibrosis (defined as LSM >= 7 kPa on Fibroscan (R)). At follow-up, 16 patients had a worsening of glycaemic control (arbitrarily defined as HbA1c increase >= 0.5% from baseline). The prevalence of NAFLD and coexisting clinically significant fibrosis at baseline was at least three times greater among patients who developed worse glycaemic control at follow-up, compared with those who did not (31.3% vs. 8.9%; p = 0.030). In logistic regression analysis, the presence of NAFLD and clinically significant fibrosis was associated with an approximately 4.5-fold increased likelihood of developing worse glycaemic control at follow-up (odds ratio 4.66, 95% confidence interval 1.07-20.3; p = 0.041), even after adjustment for baseline confounding factors, such as age, body mass index, haemoglobin A1c (or HOMA-estimated insulin resistance) and use of some glucose-lowering agents that may positively affect NAFLD and liver fibrosis. In conclusion, our results suggest that the presence of Fibroscan (R) -assessed significant fibrosis was associated with a higher risk of developing worse glycaemic control in postmenopausal women with T2DM and NAFLD.
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