睾酮作为南印度人群结直肠癌的生物标志物

Mohd Younis, Sevgi Gezici, Amrit Sudershan, Sanjeev Kumar Digra, Ashma Gupta, Arun Meyyazhagan, Parvinder Kumar, Vijaya Anand
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摘要

结直肠癌(CRC)是一种高度危及生命的疾病,死亡率很高。有人提出,睾酮水平可能在使个体易患这种毁灭性疾病的过程中起作用。睾酮主要控制男性生殖系统的成熟,同时对两性都有生理影响。在本研究中,我们调查了南印度人群中CRC患者的睾丸激素水平。在印度南部泰米尔纳德邦的医院采集血样,并选择一组健康对照进行比较分析。共有130名受试者参与了这项研究,包括65名CRC患者和同等数量的健康对照。从每个受试者身上采集约7ml血液用于放射免疫测定。使用SPSS软件对血液样本的放射免疫分析结果进行分析,以评估离散和连续数据变量之间的差异。采用卡方检验和t检验进行统计学评价。结直肠癌患者表现出显著的(P <0.0001)平均睾酮水平降低(06.68;2.15 nmol/L),与对照组(22.54 ±8.85 nmol / L)。进一步按吸烟状况分层发现,不吸烟的结直肠癌患者睾酮水平较低(06.81 ±2.21 nmol/L),比非吸烟对照组(10.15 nmol/L;2.48 nmol/L),差异有统计学意义(P <0.0001)。调整酒精摄入后,结直肠癌患者的平均睾酮水平下降(06.31;2.30 nmol/L),与对照组(07.96 ±2.45 nmol/L),差异有统计学意义(P <0.022)。这些发现支持了睾酮水平降低在结直肠癌发病机制中作为关键风险生物标志物的观点。
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Testosterone as a biomarker of colorectal cancer in the South Indian population
Colorectal cancer (CRC) is a highly life-threatening disease associated with a significant mortality rate. It has been proposed that testosterone levels may play a role in predisposing individuals to such devastating conditions. Testosterone primarily governs the maturation of the male reproductive system while also exerting physiological effects in both genders. In the present study, we investigated testosterone levels in CRC patients among the South Indian population. Blood samples were collected in the hospitals in Tamil Nadu, South India, and a cohort of healthy controls was selected for comparative analysis. A total of 130 subjects participated in the study, consisting of 65 CRC patients and an equal number of healthy controls. Approximately 7 mL of blood was collected from each subject for radioimmunoassay. The results of radioimmunoassay on the blood samples were analyzed using SPSS to assess differences between discrete and continuous data variables. Chi-square and t-tests were conducted for statistical evaluation. CRC patients exhibited significantly (P < 0.0001) reduced mean testosterone levels (06.68 &plusmn; 2.15 nmol/L) compared to controls (22.54 &plusmn; 8.85 nmol/L). Further stratification by smoking status revealed that non-smoker CRC patients had lower testosterone levels (06.81 &plusmn; 2.21 nmol/L) than non-smoking controls (10.15 &plusmn; 2.48 nmol/L), with a statistically significant difference (P < 0.0001). Adjusting for alcohol consumption, CRC patients displayed decreased mean testosterone levels (06.31 &plusmn; 2.30 nmol/L) compared to controls (07.96 &plusmn; 2.45 nmol/L), and this difference was found to be significant (P < 0.022). These findings support the notion that reduced testosterone levels serve as a critical risk biomarker in the pathogenesis of CRC.
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