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. 2022 Mar 17;13:1407. doi: 10.1038/s41467-022-28237-4

Table 1.

Cohort demographics and clinical features.

Indolent, non-dysplastic Dysplastic BE adjacent to EAC Pre-progressor p-value indolent vs dysplastic p-value indolent vs pre-progressor
Number of patients 28 62 47 12
Patient dysplasia grade ND (LGD: 16, HGD: 25, IMC: 21) NA ND
Time between ND biopsy and future dysplasia in months, median (range) NA NA NA 42.5 (15–100)
Gender, M:F 3.7:1 4.2:1 6.8:1 3:1 0.78 1
  Male 22 50 41 9
  Female 6 12 6 3
Age in years, median (range) 76 (31–83) 69 (39–86) 67 (49–84) 61 (43–77) 0.43 0.034a
BMI, median (range) 28.8 (23.2–43.9) 28.9 (13.5–40.9) 28.1 (20.3–38.8) 27.8 (24.6–34.8) 0.86 0.67
  NA 4 2 9 1
Maximum length BE segment in cm, median (range) 5 (2–12) 6 (0.5–18) Not recorded 4.5 (3–14) 0.56 0.84
Ethnicity
  White British 26 55 36 10
  White other 1 1 1 2
  Pakistani 0 1 0 0
  NA 1 5 10 0
Smoker
  Y, n (%) 10 (45.5%) 39 (81.3%) 30 (71.4%) 5 (62.5%) 0.004 0.68
  N 12 9 12 3
  NA 6 14 5 4
PPI
  Y, n (%) 26 (92.8%) 59 (96.7%) 31 (77.5%) 12 (100%) 0.59 1
  N 2 2 9 0
  NA 0 1 7 0
NSAID
  Y 10 (38.4%) 20 (32.7%) 6 (37.5%) 1 (8.3%) 0.63 0.12
  N 16 41 10 11
  NA 2 1 31 0
Surveillance pre-study sample in months, median (range) 109 (5–233) 3 (0–193) NA 48 (0–141)
Follow-up post-study sample in months, median (range) 38.5 (0–116) 35 (0–127) NA 92 (26–119)
Total patient surveillance in months, median (range) 139 (44–258) 57 (0–249) NA 154 (50–248)

Statistical comparisons were made between indolent and dysplastic, and indolent and pre-progression groups. There were significantly more smokers (p-value = 0.004) in the dysplastic vs. indolent groups. p-values calculated using Fisher’s exact test for categorical variables and t-test (two-sided) for continuous variables.

BMI body mass index, PPI proton pump inhibitor, NSAID non-steroidal anti-inflammatory drugs, ND non-dysplastic, LGD low-grade dysplasia, HGD high-grade dysplasia, IMC intramucosal carcinoma, NA not applicable, % given exclude NA patients.

aThe only significantly different variable between the indolent and pre-progressor cases was the age, with the pre-progressor cases being younger. However, this was likely due to the requirement to use a sample from early in the follow-up for pre-progressor cases.

Surveillance in months, prior to the sequenced sample, and follow-up in months after the study sample are given separately.