Key result
Childhood ALL history is linked to ~11% higher plasma ADMA levels versus healthy controls.
Why the study?
Does a history of childhood ALL treated with chemotherapy increase plasma levels of ADMA in young adult survivors compared to healthy controls?
Case-Control (n=45)
Does a history of childhood ALL treated with chemotherapy increase plasma levels of ADMA in young adult survivors compared to healthy controls?
Young adult survivors of childhood ALL treated with chemotherapy exhibit elevated ADMA levels, which may reflect late detrimental effects of chemotherapy on cardiovascular risk.
Answers are grounded in this paper and cite their sources.
May signal heightened CV risk in ALL survivors; hypothesis-generating for chemotherapy-related endothelial effects.
Background:Adult survivors of childhood malignancy are predisposed to late cardiovascular (CV) complications. Our aim was to estimate plasma levels of the endogenous nitric oxide formation inhibitor asymmetric dimethylarginine (ADMA), in long-term survivors of childhood acute lymphoblastic leukemia (ALL) treated with only chemotherapy. Methods:ADMA and its isomer symmetric dimethylarginine (SDMA) were measured in 25 former ALL patients (aged 18–28 years) who had survived without recurrent disease ≥ 5 years from completing chemotherapy without cranial irradiation, and in 20 healthy controls (aged 20–31 years). Results:Characteristics of the both groups were similar, except for lower high-density lipoproteins-cholesterol (HDL-C) in ALL survivors. Compared to controls, the former ALL patients exhibited significant, albeit small, rises in levels of ADMA (0.63 ± 0.09 [SD] vs. 0.57 ± 0.07 μmol/L;p= 0.016), but not SDMA, with a consequently increased ADMA to SDMA ratio (1.08 ± 0.22 vs. 0.91 ± 0.16;p= 0.004). The effect of former ALL on ADMA was attenuated (intergroupp= 0.10 [ANCOVA]) upon adjustment for HDL-C (ADMA vs. HDL-C regression coefficient: −0.065 ± 0.030 [SEM];p= 0.03). Conclusions:ADMA is elevated in adult childhood ALL survivors, which can reflect late detrimental chemotherapy effects, partially related to minor lipid profile changes. Whether these subtle ADMA elevations might herald future CV morbidity, remains to be elucidated.
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Sulicka‐Grodzicka et al. (2012) conducted a case-control in Childhood acute lymphoblastic leukemia (ALL) (n=45). History of childhood ALL vs. Healthy controls was evaluated on Plasma levels of asymmetric dimethylarginine (ADMA) (p=0.016). Adult survivors of childhood acute lymphoblastic leukemia exhibited significantly higher plasma levels of ADMA compared to healthy controls (0.63 vs. 0.57 μmol/L; p=0.016).
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