Tseng Chin-Hsiao
Department of Internal Medicine, National Taiwan University College of Medicine, Taipei 10051, Taiwan.
Division of Endocrinology and Metabolism, Department of Internal Medicine, National Taiwan University Hospital, Taipei 10002, Taiwan.
Cancers (Basel). 2023 Aug 26;15(17):4276. doi: 10.3390/cancers15174276.
Thiazolidinedione (TZD) exerts anti-proliferative effects on multiple myeloma (MM) cells. However, there has not been any human study investigating the risk of MM associated with TZD use.
We used Taiwan's National Health Insurance database to identify 423,949 patients who had been newly diagnosed with diabetes mellitus between 1999 and 2005. After excluding ineligible patients, 86,999 pairs of patients with and without the use of TZD (rosiglitazone or pioglitazone) that had been matched based on propensity score were selected for a follow-up for MM until 31 December 2011. The hazard ratios for MM were estimated using Cox regression and weighted using a propensity score.
After a median follow-up of 4.6 years and 4.7 years in ever users and never users of TZD, 32 and 47 cases were diagnosed with MM, respectively. A 35% lower risk (though not statistically significant) was observed among ever users (hazard ratio 0.652, 95% confidence interval: 0.416-1.023, = 0.0625). When ever users were divided by the median (15 months) cumulative duration of TZD therapy, the hazard ratios (95% confidence interval) for the lower and upper medians were 0.706 (0.394-1.264) and 0.603 (0.346-1.051), respectively. When treated as a continuous variable, the hazard ratio for every 1-month increment of the cumulative duration was 0.980 (95% confidence interval: 0.963-0.997, = 0.0185). In the age subgroup analysis, a significantly lower risk could be seen in the older age subgroup of ≥65 years (hazard ratio 0.550, 95% confidence interval: 0.305-0.992, = 0.0468). Additional analyses suggested that there were no interactions between TZD and some medications and between TZD and some clinical diagnoses, and that the use of TZD as a preventive drug for MM might not be cost-effective because a number-needed-to-treat of 5800 was too large. Survival analyses suggested that ever users had a significantly lower risk of death when all patients were analyzed (hazard ratio: 0.84, 95% confidence interval: 0.81-0.87, < 0.0001 via a log-rank test) or when patients who developed MM were analyzed (hazard ratio: 0.40, 95% confidence interval: 0.19-0.86, = 0.0153 via a log-rank test).
In Taiwanese patients with type 2 diabetes mellitus, TZD use is associated with a borderline lower risk of MM, which is more remarkable in patients aged ≥65 years. Because of the low incidence of MM, the use of TZD for the prevention of MM may not be cost-effective. Patients who have been treated with TZD may have a survival advantage. Future research is required to confirm the findings.
噻唑烷二酮(TZD)对多发性骨髓瘤(MM)细胞具有抗增殖作用。然而,尚无人体研究调查使用TZD与MM风险之间的关系。
我们利用台湾全民健康保险数据库,确定了1999年至2005年间新诊断为糖尿病的423,949例患者。排除不符合条件的患者后,选择了86,999对根据倾向得分匹配的使用TZD(罗格列酮或吡格列酮)和未使用TZD的患者,随访至2011年12月31日,观察MM发生情况。使用Cox回归估计MM的风险比,并使用倾向得分进行加权。
TZD使用者和非使用者的中位随访时间分别为4.6年和4.7年,分别有32例和47例被诊断为MM。TZD使用者的风险降低了35%(尽管无统计学意义)(风险比0.65.6,95%置信区间:0.416 - 1.023,P = 0.0625)。当将TZD使用者按TZD治疗的中位累积持续时间(15个月)分为两组时,较低和较高累积持续时间组的风险比(95%置信区间)分别为0.706(0.394 - 1.264)和0.603(0.346 - 1.051)。将累积持续时间作为连续变量分析时,每增加1个月的累积持续时间,风险比为0.980(95%置信区间:0.963 - 0.997,P = 0.0185)。在年龄亚组分析中,≥65岁的老年亚组风险显著降低(风险比0.550,95%置信区间:0.305 - 0.992,P = 0.0468)。进一步分析表明,TZD与某些药物以及TZD与某些临床诊断之间无相互作用,并且由于需治疗人数高达5800,使用TZD作为MM的预防药物可能不具有成本效益。生存分析表明,在分析所有患者时(风险比:0.84,95%置信区间:0.81 - 0.87,通过对数秩检验P < 0.0001)或分析发生MM患者时(风险比:0.40,95%置信区间:0.19 - 0.86,通过对数秩检验P = 0.0153),TZD使用者的死亡风险显著较低。
在台湾2型糖尿病患者中,使用TZD与MM风险略有降低相关,在≥65岁患者中更显著。由于MM发病率低,使用TZD预防MM可能不具有成本效益。接受TZD治疗的患者可能具有生存优势。需要进一步研究来证实这些发现。