The Impact of SCN9A Gene Polymorphism on Individual Pain Perception in the General Population

Xianwei Zhang

Status: Completed

Conditions: Surgery; Pain

Study type: Observational

Funder types: Other

Identifiers

NCT01507493

SCN9A

Details and patient eligibility

About

This study was conducted to explore whether the non-synonymous single-nucleotide polymorphisms in SCN9A gene can predict individual basal pain perception and postoperative pain intensity in the general population undergoing upper abdominal surgery. Methods: Patients receiving elective upper abdominal surgery under general anesthesia were recruited into this study. Genotyping of SCN9A was carried out by direct sequencing. The investigators measured their preoperative pressure pain threshold (PPT) and pressure pain tolerance (PTO). The visual analog scale (VAS) was used for pain evaluation at rest during patient-controlled analgesia (PCA) treatment 0 h, 12 h ,24 h and 48h after operation. And the PCA press frequency and drug consumption were recorded.

Full description

Patients with the following diseases were excluded: known history of chronic pain, psychiatric diseases or communication disorders, diabetes mellitus, severe cardiovascular diseases, kidney or liver diseases with poor hepatic function, alcohol or drug abuse, heavy smoker, pregnancy or at the lactation period.

Enrollment: 200 patients

Sex: All

Ages: 20 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Aged 20-70 years
• Receiving elective upper abdominal surgery
• Anesthesiologists (ASA) physical status I or II
• Received PCA administration
• Agreed to participate the research

Exclusion criteria

• History of chronic pain
• Psychiatric diseases
• Diabetes mellitus
• Severe cardiovascular diseases
• Kidney or liver diseases
• Alcohol or drug abuse
• Heavy smoker
• Pregnancy or at lactation period
• Refused PCA administration
• Disagree to participate to the research

Trial design

200 participants in 2 patient groups

mutant alleles

Description:

grouped by SCN9A mutant alleles including 3312T, 1719R, 1150W.

wild-type alleles

Description:

grouped by SCN9A wild-type alleles including 3312G, 1719C, 1150R.