» Articles » PMID: 25310024

Abdominal Regional Fat Distribution on MRI Correlates with Cholecystolithiasis

Overview
Journal PLoS One
Date 2014 Oct 14
PMID 25310024
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Aims: To determine whether abdominal regional fat distribution pattern on MRI is correlated with cholecystolithiasis.

Methods: Magnetic resonance imaging (MRI) of 163 patients with cholecystolithiasis and 163 non-cholecystolithiasis control subjects admitted to our institution between March 2011 and September 2013 were included in this cross-sectional evaluation. There were 98 women and 65 men in cholecystolithiasis group with an average age of 57±16 years (range 25-86 years). There were 87 women and 76 men in the control group with an average age of 41±16 years (range 14-77 years). Visceral adipose tissue (VAT), abdominal subcutaneous adipose tissue (SAT) and total abdominal adipose tissue (TAT) of all the subjects at navel level were measured on abdominal MRI. According to the visceral adipose area (cut-off point VAT = 100 cm2), study subjects were divided into 1) increased accumulation of intra-abdominal fat and 2) normal distribution of intra-abdominal fat. Logistic regression was used to assess the association of fat with the presence of cholecystolithiasis, adjusted for age and sex.

Results: The incidence of increased intra-abdominal fat accumulation in the cholecystolithiasis group was significantly higher than that of the control group (P = 0.000). After adjusting for age and sex, cholecystolithiasis was associated with a one standard deviation increment in the waist circumference (WC) (OR = 1.44; 95%CI: 1.01,1.93; p = 0.00), VAT (OR = 4.26; 95%CI: 1.85,5.29; p = 0.00), VAT/SAT (OR = 8.66; 95%CI: 1.60,12.63; p = 0.00), and VAT/TAT (OR = 6.73; 95%CI: 4.24,12.18; p = 0.00), but not with fat content in the abdominal subcutaneous fat (p = 0.19).

Conclusions: The visceral adipose tissue and distribution proportion of abdominal adipose tissue are correlates of cholecystolithiasis.

Citing Articles

Genetically predicted visceral adipose tissue and risk of nine non-tumour gastrointestinal diseases: evidence from a Mendelian randomization study.

Sun X, Yuan Y, Chen L, Ye M, Zheng L Int J Obes (Lond). 2023; 47(5):406-412.

PMID: 36934207 DOI: 10.1038/s41366-023-01279-4.


Relationship of Two-Hour Plasma Glucose and Abdominal Visceral Fat with Bone Mineral Density and Bone Mineral Content in Women with Different Glucose Metabolism Status.

Jia X, Liu L, Wang R, Liu X, Liu B, Ma N Diabetes Metab Syndr Obes. 2020; 13:851-858.

PMID: 32256099 PMC: 7093093. DOI: 10.2147/DMSO.S245096.

References
1.
Lambou-Gianoukos S, Heller S . Lithogenesis and bile metabolism. Surg Clin North Am. 2008; 88(6):1175-94, vii. DOI: 10.1016/j.suc.2008.07.009. View

2.
Bowen J, Brenner H, FERRANTE W, Maule W . Gallstone disease. Pathophysiology, epidemiology, natural history, and treatment options. Med Clin North Am. 1992; 76(5):1143-57. DOI: 10.1016/s0025-7125(16)30313-3. View

3.
Wang W, Wu Z, Zhao D, Wu G, Wang W, Liu J . [The trends of body mass index and overweight in population aged 25 - 64 in Beijing during 1984 - 1999]. Zhonghua Liu Xing Bing Xue Za Zhi. 2003; 24(4):272-5. View

4.
Shaffer E . Epidemiology and risk factors for gallstone disease: has the paradigm changed in the 21st century?. Curr Gastroenterol Rep. 2005; 7(2):132-40. DOI: 10.1007/s11894-005-0051-8. View

5.
Einarsson K, Nilsell K, Leijd B, Angelin B . Influence of age on secretion of cholesterol and synthesis of bile acids by the liver. N Engl J Med. 1985; 313(5):277-82. DOI: 10.1056/NEJM198508013130501. View