Pérez de Oteyza C, Menéndez Martínez M A, Irazábal C, Enríquez de Salamanca R, Pérez Aznar C, Rebollar J L
Departamento de Medicina Interna, Hospital Militar Universitario Gómez Ulla, Universidad Complutense, Madrid.
An Med Interna. 1996 May;13(5):217-21.
To establish the discriminatory value of ADA and beta 2M serum levels as markers of AIDS progression.
We have followed quarterly during two years a cohort of 24 patients with HIV infection; 103 clinical and laboratory evaluations were done (CDC/93 classification). In each of those blood samples we determined ADA, beta 2M, IgG, IgA, IgM, and CD4+ and CD8+ lymphocytes.
26 evaluations belong to cases that kept stable in the clinic category A or B, CDC/93, ("stables": ADA = 19.05 +/- 10.79 U/L; beta 2M = 2.95 +/- 1.1 mg/L); the remaining 77 evaluations are from patients who clinical progressed to AIDS ("progressors": ADA = 32.03 +/- 13.2 U/L; beta 2M = 4.74 +/- 1.94 mg/L). When we compared statistically (RSIGMA software) the ADA and beta 2M means of both groups (Student t) and the means of all the variables in a block (multivariate analysis: Hotelling T2), very significant differences were appreciated (p < 0.001).
ADA and beta 2M are significantly increased in serum of HIV infected patients who clinical progress to AIDS. ADA and beta 2M can be used as serum markers of AIDS progression with a mistaken classification probability in the discriminatory analysis of 0.25; this probability decreases to 0.06 when immunoglobulins and lymphocytes subpopulations are evaluated too.
确定腺苷脱氨酶(ADA)和β2微球蛋白(β2M)血清水平作为艾滋病进展标志物的鉴别价值。
我们对24例HIV感染患者进行了为期两年的季度随访;进行了103次临床和实验室评估(CDC/93分类)。在每一份血样中,我们测定了ADA、β2M、IgG、IgA、IgM以及CD4+和CD8+淋巴细胞。
26次评估属于在临床A类或B类(CDC/93)中保持稳定的病例(“稳定组”:ADA = 19.05 ± 10.79 U/L;β2M = 2.95 ± 1.1 mg/L);其余77次评估来自临床进展为艾滋病的患者(“进展组”:ADA = 32.03 ± 13.2 U/L;β2M = 4.74 ± 1.94 mg/L)。当我们使用RSIGMA软件进行统计学比较(两组的ADA和β2M均值采用Student t检验,所有变量均值采用多变量分析:Hotelling T2)时,发现了非常显著的差异(p < 0.001)。
临床进展为艾滋病的HIV感染患者血清中ADA和β2M显著升高。ADA和β2M可作为艾滋病进展的血清标志物,在鉴别分析中的错误分类概率为0.25;当同时评估免疫球蛋白和淋巴细胞亚群时,该概率降至0.06。