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. Author manuscript; available in PMC: 2021 May 1.
Published in final edited form as: Pain. 2020 May;161(5):1052–1064. doi: 10.1097/j.pain.0000000000001792

Table 6:

Haplotype association to analyze the relationship between acute pain phenotypes and EREG haplotypes:

Cohort Acute Pain Phenotype n prevalence Haplotype II Haplotype III
ESTIMATE FDR ESTIMATE FDR
OPPERA Acute pain intensity 213 52.58%Ϯ β = −1.83 0.517 β = 8.68 0.0390*
Acute facial pain OR = 0.76 0.289 OR = 1.99 0.121
UK biobank Acute pain all over the body 335,565 0.87 % OR = 1.01 0.909 OR = 1.33 0.0003**
Acute stomach or Abdominal pain 352,780 5.34 % OR = 0.99 0.261 OR = 0.94 0.066
Acute headache 388,126 13.96 % OR = 0.99 0.246 OR = 1.00 0.771
Acute neck or shoulder pain 369,264 9.57 % OR = 1.02 0.083 OR = 1.01 0.611
Acute back pain 373,432 10.58 % OR = 0.99 0.672 OR = 0.98 0.447
Acute hip pain 346,291 3.57 % OR = 0.99 0.820 OR = 0.98 0.758
Acute knee pain 356,768 6.40 % OR = 1.00 0.810 OR = 1.03 0.408
Acute facial pain 338,577 1.37 % OR = 0.97 0.405 OR = 0.95 0.541
No. of acute pain sites 471,773 29.22 %Δ β = −0.001 0.752 β = 0.028 0.003*
At least one acute pain site OR = 1.01 0.909 OR = 1.34 0.0002**

CPI: characteristic pain intensity; n: valid number of participants/cases and controls; number of controls (no pain at all) is 333,936 for all the UK biobank phenotypes;

Ϯ

prevalence of participants with acute pain intensity at follow-up > 0 among n with valid acute acute pain intensity scores at follow-up; β: slope of least – squares line; OR: Odds Ratio;

Δ

prevalence of at least one acute pain site. FDR: False Discovery Rate;

‘**’:

FDR < 0.001

‘*’:

0.05