Alexanderson B, Evans D A, Sjöqvist F
Br Med J. 1969 Dec 27;4(5686):764-8. doi: 10.1136/bmj.4.5686.764.
Nineteen identical (monozygotic) and 20 fraternal (dizygotic) sets of twins between 45 and 51 years of age were given nortriptyline orally in doses of 0.2 mg./kg. body weight three times daily for eight days. The steady-state plasma concentrations of nortriptyline were calculated from the mean of the determinations for days 6, 7, and 8. Identical twins, not treated with other drugs, achieved similar steady-state plasma concentrations of nortriptyline in contrast to fraternal twins who were not given other drugs. The intrapair similarity in steady-state plasma concentrations was not found in identical twins simultaneously treated with various drugs during the experiment. Identical and fraternal twins treated with drugs containing barbiturates had considerably lower steady-state plasma concentrations of nortriptyline compared with untreated twins.It is concluded that most of the variability in nor-triptyline steady-state plasma concentration between persons who have not received drugs is genetically determined. Exposure to other drugs also influences the steady-state plasma concentration of nortriptyline, which in a given patient may therefore be determined by a resultant of genetic and environmental factors.
19对45至51岁的同卵双胞胎和20对异卵双胞胎口服去甲替林,剂量为0.2毫克/千克体重,每日3次,共8天。去甲替林的稳态血浆浓度根据第6、7和8天测定值的平均值计算得出。未服用其他药物的同卵双胞胎,其去甲替林的稳态血浆浓度相似,而未服用其他药物的异卵双胞胎则不然。在实验期间同时服用各种药物的同卵双胞胎中,未发现稳态血浆浓度的配对内相似性。与未治疗的双胞胎相比,服用含巴比妥类药物的同卵和异卵双胞胎的去甲替林稳态血浆浓度显著降低。得出的结论是,未接受药物治疗的个体之间,去甲替林稳态血浆浓度的大部分变异性是由基因决定的。接触其他药物也会影响去甲替林的稳态血浆浓度,因此在特定患者中,这可能由遗传和环境因素的综合作用决定。