COMMENT ON PARENTE ET AL.
The Relationship Between Body Fat
Distribution and Nonalcoholic Fatty
Liver in Adults With Type 1 Diabetes.
Diabetes Care 2021;44:1706–1713
Diabetes Care 2022;45:e7 | https://doi.org/10.2337/dc21-1773
Marieke de Vries,
Karin H.A.H. Kaasjager, and
Harold W. de Valk
With great interest we read the recent
study by Parente et al. (1), in which they
report a clear relationship between body
fat distribution and nonalcoholic fatty
liver (NAFL) in patients with type 1 diabe-
tes. Visceral adipose tissue as measured
with DXA was independently associated
with NAFL (MRI assessed prevalence,
11.6%), whereas peripheral and total
body fat were not. In addition, waist-to-
height-ratio (WHtR) was more strongly
associated with NAFL than BMI. Based
on this, they state that WHtR might be
an easy and inexpensive tool to screen
individuals with type 1 diabetes at higher
risk for NAFL.
Here, we would like to present pre-
liminary results from our own study,
which are comparable to the findings of
Parente et al. (1) and support the idea
of using clinical markers of visceral fat
as a screening tool for NAFL in patients
with type 1 diabetes.
We performed a NAFL study in 150
patients with type 1 diabetes. Patient
characteristics were comparable to those
of Parente et al. (1): mean age, 47 ± 14
years; male, 55%; diabetes duration,
25 ± 14 years; and median BMI, 25 kg/m
2
.
We assessed NAFL by transient elastog-
raphy controlled attenuation parameter
(CAP) (CAP cutoff $248 dB/m) (2) and
found a NAFL prevalence of 34% (n =
51). In the total group, central obesity
(WHtR $0.5) was present in 85% of
patients, in the NAFL group in as much
as 88.2%, and in the non-NAFL group in
only 44.4%. The area under the curve
(AUC) of the receiver operating charac-
teristic curve of the association between
WHtR and NAFL was 0.76 (95% CI
0.68–0.84), and that of the association of
BMI and NAFL was 0.71 (95% CI
0.62–0.80). The difference in AUC of
WHtR and BMI was borderline statisti-
cally significant (P = 0.05, calculated by
permutation analysis [3]). We found an
optimal (Youden) cutoff value for WHtR
of 0.51, with a sensitivity of 86% and
specificity of 62%. For BMI, the optimal
cutoff value was 25.2 kg/m
2
, with a sen-
sitivity of 72% and specificity of 67%.
To extend the conclusion of Parente
et al. (1) that easy and low-cost markers
of visceral fat might help identify patients
at need for further hepatic imaging, we
also assessed the AUC for waist circum-
ference (WC), measured at the level of
the iliac crest. The AUC of WC (0.80, 95%
CI 0.71–0.88) was larger than that of BMI
(P < 0.001) and that of WHtR (P = 0.06).
For WC, the optimal cutoff for male
patients was 92.5 cm (sensitivity, 87%;
specificity 69%), and for female patients
it was 94.5 cm (sensitivity, 65%; specific-
ity, 72%).
In conclusion, we endorse that clini-
cal markers of visceral adipose tissue
(WHtR and WC) are strongly associated
with NAFL in patients with type 1 dia-
betes and might indeed be of help in
choosing wisely in clinical practice to
identify patients in need of further
hepatic imaging.
Duality of Interest. No potential conflicts
of interest relevant to this letter were
reported.
References
1. Parente EB, Dahlstr€ om EH, Harjutsalo V,
et al.; FinnDiane Study Group. The relationship
between body fat distribution and nonalcoholic
fatty liver in adults with type 1 diabetes.
Diabetes Care 2021;44:1706–1713
2. Karlas T, Petroff D, Sasso M, et al.
Individual patient data meta-analysis of
controlled attenuation parameter (CAP)
technology for assessing steatosis. J Hepatol
2017;66:1022–1030
3. Venkatraman ES, Begg CB. A distribution-free
procedure for comparing receiver operating
characteristic curves from a paired experi-
ment. Biometrika 1996;83:835–848
Department of Internal Medicine, University Medical Center Utrecht, Utrecht, the Netherlands
Corresponding author: Marieke de Vries, m.devries-19@umcutrecht.nl
© 2021 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not
for profit, and the work is not altered. More information is available at https://www.diabetesjournals.org/journals/pages/license.
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Diabetes Care Volume 45, January 2022 e7
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