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Association of OPRM1, MIR23B, and MIR107 genetic variability with acute pain, chronic pain and adverse effects after postoperative tramadol and paracetamol treatment in breast cancer Cover

Association of OPRM1, MIR23B, and MIR107 genetic variability with acute pain, chronic pain and adverse effects after postoperative tramadol and paracetamol treatment in breast cancer

Open Access
|Mar 2023

Figures & Tables

The impact of investigated polymorphisms on chronic and neuropathic pain (N = 101)

SNPGenotypeChronic N (%) painOR (95% CI)POR (95% CI)adjPadj
OPRM1 rs1799971AA15 (20.3)Ref. Ref.
AG+GG6 (22.2)1.12 (0.39–3.28)0.8311.2 (0.4–3.57)0.739
OPRMrs677830 1CC14 (27.5)Ref. Ref.
CT+TT7 (14)0.43 (0.16–1.18)0.1010.44 (0.16–1.21)0.112
MIR23B rs1011784CC9 (15.3)Ref. Ref.
CG10 (32.3)2.65 (0.94–7.45)0.0652.85 (0.99–8.19)0.052
GG2 (20)1.39 (0.25–7.64)0.7061.68 (0.29–9.83)0.563
MIR107 rs2296616CG+GG GG12 (29.3) 0 (0)2.3 (0.86–6.11) Ref.0.0952.58 (0.94–7.1) Ref.0.067
GA9 (18.4)/0.099*
AA12 (35.3)/0.004*
GA+AA21 (25.3)/0.021*
SNPGenotypeNeuropathic pain N (%)OR (95% CI)POR (95% CI)adjPadj
OPRM1 rs1799971AA19 (25.7)Ref. Ref.
AG+GG6 (22.2)0.83 (0.29–2.36)0.7220.94 (0.32–2.75)0.915
OPRMrs677830 1CC17 (33.3)Ref. Ref.
CT+TT8 (16)0.38 (0.15–0.99)0.0470.4 (0.15–1.04)0.060
MIR23B rs1011784CC11 (18.6)Ref. Ref.
CG12 (38.7)2.76 (1.04–7.31)0.0423.25 (1.17–9.02)0.023
GG2 (20)1.09 (0.2–5.87)0.9191.59 (0.27–9.24)0.607
CG+GG14 (34.1)2.26 (0.9–5.68)0.0822.85 (1.07–7.59)0.036
MIR107 rs2296616GG3 (16.7)Ref. Ref.
GA11 (22.4)1.45 (0.35–5.93)0.6071.37 (0.33–5.69)0.666
AA11 (32.4)2.39 (0.57–10.02)0.2332.34 (0.55–9.97)0.249
GA+AA22 (26.5)1.8 (0.48–6.83)0.3861.73 (0.45–6.65)0.424

Patients’ clinical characteristics



All subjects
Stronger postoperative analgesia with tramadol/paracetamol
Weaker postoperative analgesia with tramadol/paracetamol
Sample size

N = 113
N = 55
N = 58
Characteristic N (%)N (%)N (%)
Age (years)Median (25–75 %)55 (48–63)57 (49–64)53,5 (47.8–61)
Weight (kg)Median (25–75 %)72 (63.5–82)72 (64–82)72 (63–82.3)
Body Mass Index (kg/m2)Median (25–75 %)27.1 (23.4–31.0)26.7 (23.0–30.8)27.6 (23.5–31.2)
SmokingNo87 (77.7) [1]41 (75.9) [1]46 (79.3)
Yes25 (22.3)13 (24.1)12 (20.7)
ASA score122 (19.6) [1]10 (18.2)12 (21.1) [1]
281 (72.3)39 (70.9)42 (73.7)
39 (8.0)6 (10.9)3 (5.3)
Side of the operationLeft62 (54.9)30 (54.5)32 (55.2)
Right50 (44.2)24 (43.6)26 (44.8)
Bilateral1 (0.9)1 (1.8)0 (0.0)
Tumor grade14 (3.6) [1]1 (1.9) [1]3 (5.2)
1–23 (2.7)2 (3.7)1 (1.7)
239 (34.8)17 (31.5)22 (37.9)
2–38 (7.1)2 (3.7)6 (10.3)
358 (51.3)32 (59.3)26 (44.8)
VAS after 7 daysMedian (25–75 %)2 (1–3) [5]1.3 (1–2) [3]2 (1–3) [2]
VAS after 14 daysMedian (25–75 %)1.5 (0–2) [11]1 (0–2) [9]2 (1–2) [2]
VAS after 21 daysMedian (25–75 %)1 (0.4–2) [11]1 (0–2) [9]1 (1–2) [2]
VAS after 28 daysMedian (25–75 %)1 (0–2) [14]1 (0–1) [10]1 (1–2) [4]

The investigated polymorphism’s characteristics and frequencies

GeneSNPGenotypeN (%)PAF (%)MAF HapMap CEU expected (%)PHWE
OPRM1rs1799971AA84 (74.3)14.215.6–16.70.570
AG26 (23.0)
GG3 (2.7)
rs677830CC56 (49.6)27.420.70.098
CT52 (46.0)
TT5 (4.4)
MIR23Brs1011784*CC63 (56.3) [1]26.823.30.153
CG38 (33.9)
GG11 (9.8)
MIR107rs2296616*GG21 (18.6)57.154.2–55.30.944
GA55 (48.7)
AA37 (32.7)

The impact of investigated polymorphisms on constipation anytime during the first four weeks of tramadol treatment (N = 99)

SNPGenotypeConstipation anytime N (%)OR (95% CI)POR (95% CI)adjPadj
OPRM1 rs1799971AA30 (40)Ref. Ref.
AG+GG18 (75)4.5 (1.6–12.64)0.0044.31 (1.52–12.17)0.006
OPRM1 rs677830CC24 (48)Ref. Ref.
CT+TT24 (49)1.04 (0.47–2.29)0.9220.98 (0.44–2.19)0.964
MIR23B rs1011784CC29 (50)Ref. Ref.
CG16 (50)1 (0.42–2.37)1.0000.96 (0.4–2.31)0.930
GG3 (37.5)0.6 (0.13–2.75)0.5100.46 (0.1–2.23)0.338
CG+GG19 (47.5)0.9 (0.4–2.03)0.8080.84 (0.37–1.91)0.676
MIR107 rs2296616GG11 (57.9)Ref. Ref.
GA23 (48.9)0.7 (0.24–2.04)0.5110.73 (0.25–2.16)0.566
AA14 (42.4)0.54 (0.17–1.68)0.2850.53 (0.17–1.67)0.276
GA+AA37 (46.3)0.63 (0.23–1.72)0.3640.64 (0.23–1.77)0.386

The impact of investigated miRNA polymorphisms on nausea after 21 and 28 days of tramadol treatment (N = 99)

SNPGenotypeNausea days N (%) 21OR (95% CI)PNausea days N (%) 28OR (95% CI)P
MIRrs1011784 23BCC9 (16.4)Ref. 4 (7.5)Ref.
CG4 (12.9)0.76 (0.21–2.7)0.6685 (16.1)2.36 (0.58–9.54)0.230
GG2 (25)1.7 (0.3–9.83)0.5513 (37.5)7.35 (1.27–42.6)0.026
CG+GG6 (15.4)0.93 (0.3–2.86)0.8988 (20.5)3.16 (0.88–11.39)0.078
MIRrs2296616 107GG6 (31.6)Ref. 2 (10.5)Ref.
GA4 (8.9)0.21 (0.05–0.87)0.0314 (8.7)0.81 (0.14–4.84)0.817
AA5 (16.7)0.43 (0.11–1.69)0.2296 (21.4)2.32 (0.41–12.96)0.338
GA+AA9 (12)0.30 (0.09–0.97)0.04510 (13.5)1.33 (0.27–6.64)0.730
DOI: https://doi.org/10.2478/raon-2023-0003 | Journal eISSN: 1581-3207 | Journal ISSN: 1318-2099
Language: English
Page range: 111 - 120
Submitted on: Sep 14, 2022
Accepted on: Sep 28, 2022
Published on: Mar 22, 2023
Published by: Association of Radiology and Oncology
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2023 Zala Vidic, Katja Goricar, Branka Strazisar, Nikola Besic, Vita Dolzan, published by Association of Radiology and Oncology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.