Walitza Susanne, Kämpf Kristina, Artamonov Natalia, Romanos Marcel, Gnana Oli Rajaraman, Wirth Susanne, Warnke Andreas, Gerlach Manfred, Stopper Helga
Department of Child and Adolescent Psychiatry and Psychotherapy, University of Wuerzburg, Fuechsleinstr. 15, 97080 Wuerzburg, Germany.
Toxicol Lett. 2009 Jan 10;184(1):38-43. doi: 10.1016/j.toxlet.2008.10.011. Epub 2008 Oct 28.
Attention-deficit/hyperactivity disorder (ADHD) is the most frequent psychiatric disorder in children and adolescents and is often treated with methylphenidate (MPH), resulting in MPH exposure in more than 1% of all children in many countries. A 2005 report on cytogenetic effects in peripheral lymphocytes from 12 ADHD children treated for 3 months with MPH raised questions about its genetic toxicity and potential carcinogenicity. In 2007, we described no elevated micronucleus frequency in 21 children after 3 months of MPH-treatment; since the difference between the two studies could not be explained we now enlarged the overall sample size, and added a healthy control group, a new chronically treated group and positive control slides. Furthermore, micronuclei were analyzed in a second tissue, buccal mucosa.
A healthy control group (23 individuals), a chronically MPH-treated (>12 months) group (21 patients), and a drug naïve group of ADHD-affected children (26 patients), which was analyzed again after 3 months (17 patients) and 6 months (11 patients), provided samples for analysis of micronucleated lymphocytes. With inclusion of 14 previously obtained blood samples, an overall group size of 31 patients was reached for the comparison of the 3 months observation time with before for micronucleated lymphocytes. For buccal mucosa cells, an additional inclusion of 10 more chronically treated patients (no lymphocytes donated) yielded sample numbers of 22 (healthy), 17 (chronically treated), 23 (ADHD drug naïve), 14 (3 months) and 11 (6 months).
No significant alteration in genomic damage as seen as micronucleus frequency in peripheral lypmphocytes or buccal mucosa cells was detected after MPH treatment.
No indication for genomic damage induced by MPH was obtained in this study, as in our previous study. Together with our previous study, our overall number of MPH-treated patients is now 68 (30 chronically treated, 38 prospectively followed), plus 23 healthy controls. Ongoing studies in the USA, as well as continuation of recently published epidemiological cancer incidence analysis should provide additional reassurance for MPH-treated ADHD patients.
注意力缺陷多动障碍(ADHD)是儿童和青少年中最常见的精神疾病,常使用哌甲酯(MPH)进行治疗,在许多国家超过1%的儿童都有MPH暴露经历。2005年一份关于12名接受MPH治疗3个月的ADHD儿童外周淋巴细胞细胞遗传学效应的报告引发了对其遗传毒性和潜在致癌性的质疑。2007年,我们报道了21名儿童接受MPH治疗3个月后微核频率未升高;由于两项研究结果的差异无法解释,我们现在扩大了总体样本量,并增加了一个健康对照组、一个新的长期治疗组和阳性对照玻片。此外,还在第二种组织颊黏膜中分析了微核。
一个健康对照组(23人)、一个长期接受MPH治疗(>12个月)的组(21名患者)以及一组未接受过药物治疗的ADHD儿童(26名患者),该组在3个月(17名患者)和6个月(11名患者)后再次接受分析,提供了用于分析微核淋巴细胞的样本。加上之前获得的14份血样,在3个月观察期时,用于比较微核淋巴细胞的总体样本量达到31名患者。对于颊黏膜细胞,另外纳入10名长期治疗的患者(未捐献淋巴细胞)后,样本数量分别为22名(健康)、17名(长期治疗)、23名(未接受ADHD药物治疗)、14名(3个月)和11名(6个月)。
MPH治疗后,在外周淋巴细胞或颊黏膜细胞中,未检测到微核频率所反映的基因组损伤有显著改变。
与我们之前的研究一样,本研究未发现MPH诱导基因组损伤的迹象。连同我们之前的研究,目前接受MPH治疗的患者总数为68名(30名长期治疗,38名前瞻性随访),外加23名健康对照。美国正在进行的研究以及最近发表的癌症发病率流行病学分析的延续,应为接受MPH治疗的ADHD患者提供更多的安心保障。