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. 2024 Jan 26;5(2):101391. doi: 10.1016/j.xcrm.2023.101391

Table 2.

Results from the prospective observational study of the association between IPFD and incidence of PDAC in the UK Biobank

Cumulative incidence,a %
Crude
Age and BMI adjusted
Multivariable adjustedb
(N cases/N total) HR (95% CI)c p value HR (95% CI)c p value HR (95% CI)c p value
Categorization (mean value)d
 Low IPFD (≤10%) 0.07 (12/17,978) 1.00 (reference) 1.00 (reference) 1.00 (reference)
 High IPFD (>10%) 0.28 (32/11,485) 4.20 (2.16–8.15) <0.001 3.53 (1.72–7.26) 0.001 3.35 (1.60–7.00) 0.001
Categorization (tertiles)
 Low IPFD (≤5.8%) 0.06 (6/9,821) 1.00 (reference) 1.00 (reference) 1.00 (reference)
 Moderate IPFD (5.8–11%) 0.09 (9/9,821) 1.49 (0.53–4.19) 0.45 1.34 (0.47–3.87) 0.58 1.28 (0.44–3.73) 0.65
 High IPFD (>11%) 0.30 (29/9,821) 4.83 (2.01–11.6) <0.001 3.85 (1.47–10.1) 0.006 3.57 (1.32–9.62) 0.012
Continuous IPFDe
 IPFD (per 1-SD increase) 0.15 (44/29,463) 1.69 (1.25–2.27) 0.001 1.48 (1.05–2.08) 0.025 1.42 (0.99–2.02) 0.056

IPFD, intra-pancreatic fat deposition; PDAC, pancreatic ductal adenocarcinoma; HR, hazard ratio; CI, confidence interval; BMI, body mass index; SD, standard deviation.

a

Median follow-up period was 4.5 years (interquartile range: 3.8–5.4).

b

The multivariable analysis was adjusted for age, gender, BMI, current smoking status, and daily drinking.

c

HR and 95% CI estimated using Cox regression models.

d

High and low IPFD were defined based on the mean IPFD among all participants (10%).

e

Log transformation was applied to continuous IPFD to correct for skewness. Models evaluated 1-SD increase in the log-transformed value.