Department of Pathology, Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, TN, USA.
Ther Adv Hematol. 2011 Jun;2(3):141-5. doi: 10.1177/2040620711408490.
Between January 1999 and December 2008, 469 patients treated for acute myeloid leukemia (AML) were included in this single-institution study.
We performed a case-control analysis to study the rate of obesity among patients with acute promyelocytic leukemia (APL) and non-APL AML.
A total of 81% of APL patients analyzed were obese compared with 41.7% in the non-APL group (p < 0.001). Body mass index (BMI) >30 was seen in 57% of APL patients compared with 31% for the non-APL group (p = 0.01). Neither obesity nor the chemotherapy dosing based on ideal body weight affected survival.
Our findings generate the hypothesis that APL and metabolic syndromes may share a common pathogenic pathway via retinoic acid receptors (RARs), the ligand-controlled transcription factors that function as heterodimers with retinoid X receptors (RXRs) to regulate cell growth and survival. If this link is confirmed in larger studies, our data will instigate further studies using RXR and RAR modulators as a preventive strategy among obese individuals.
1999 年 1 月至 2008 年 12 月,共有 469 例急性髓细胞白血病(AML)患者接受了本机构的治疗。
我们进行了病例对照分析,研究了急性早幼粒细胞白血病(APL)和非 APL AML 患者中肥胖的发生率。
在接受分析的 APL 患者中,肥胖患者占 81%,而非 APL 组为 41.7%(p<0.001)。57%的 APL 患者体重指数(BMI)>30,而非 APL 组为 31%(p=0.01)。肥胖或根据理想体重进行化疗剂量调整均不影响生存。
我们的发现提出了一个假设,即 APL 和代谢综合征可能通过视黄酸受体(RARs)共享一个共同的致病途径,RARs 是配体控制的转录因子,与视黄醇 X 受体(RXRs)形成异二聚体,调节细胞生长和存活。如果在更大的研究中证实了这一联系,我们的数据将促使进一步研究使用 RXR 和 RAR 调节剂作为肥胖个体的预防策略。