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第45卷第2期 蔡清清,尤含笑,王 磊,等. NLR和SII对抗MDA5抗体阳性皮肌炎伴快速进展型肺炎的预后价值[J].
                  2025年2月                     南京医科大学学报(自然科学版),2025,45(2):196-207                        ·199 ·


                12.57)years vs.(50.16±13.36)years,P=0.03],had low⁃  (i.e.,age,NLR,LMR,SII,SIRI,AISI,and myasthenia)
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                er LYC levels(median:0.73×10 /L vs. 0.98×10 /L,P=  were included in the multivariate model. The multivari⁃
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                0.003),lower PLT levels(median:168.00 × 10 /L vs.  ate Cox regression analysis indicated that a high SII
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                179.00×10 /L,P=0.023),higher NLR levels(6.74 vs.  was an independent risk factor for mortality(HR=1.00,
                3.92,P=0.003),higher SII levels(1 206.81 vs. 716.83,  95% CI:1.00-1.00,P < 0.05). Increasing age was also
                P=0.014),higher AST levels(median:62.40 U/L vs.   a significant determinant of mortality risk(Table 3).
                48.60 U/L,P=0.005),higher LDH levels(median:      2.3  Analysis of the value of NLR and SII on the

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                344.00 U/L vs. 288.00 U/L,P=0.012),higher CRP     prognosis of anti⁃MDA5 DM
                levels(median:9.15 mg/L vs. 3.96 mg/L,P=0.001),       NLR and SII were identified as independent risk
                and higher SF levels(median:977.70 mg/mL vs.      factors for poor prognosis,specifically for the develop⁃
                547.20 mg/mL,P=0.001)(Table 1).                   ment of RPILD and overall survival,respectively. The
                    Furthermore,we observed a significant difference  ROC curve analysis was used to determine the optimal
                in myositis⁃associated antibodies,with a higher rate of  cut⁃off values for predicting RPILD and survival(Fig⁃
                anti⁃Ro52 antibody positivity in the RPILD group than  ure 1A,B). The AUC for NLR in predicting RPILD
                in the non ⁃ RPILD group(86.49% vs. 67.82% ,P=    was 0.67,with a cut⁃off value of 6.12. This cut⁃off value
                0.044). Baseline data of glucocorticoid(GC)usage also  indicated a sensitivity of 56.76% and a specificity of
                differed significantly between the two groups(P=  77.01%,suggesting moderate accuracy. Similarly,the
                0.014). In the non⁃RPILD group,27 cases(31.03%)   AUC for NLR in predicting survival was 0.73,with the
                used no GC at baseline,26 cases(29.89%)used high⁃  same cut ⁃ off value of 6.12,reflecting a sensitivity of
                dose GC,and only 1 case(1.15%)used mega⁃dose GC.  62.16% and a specificity of 79.31%,indicating a good
                In contrast,in the RPILD group,17 cases(45.95%)   accuracy. Regarding SII,the AUC for predicting
                used no GC at baseline,16 cases(43.24%)used high⁃  RPILD was 0.64,with a cut⁃off value of 1 200.82,dem⁃
                dose GC,and none used mega⁃dose GC. There were no  onstrating a sensitivity of 51.35% and a specificity of
                statistically significant differences between the two  78.16%. The AUC for SII predicting survival was 0.69,
                groups regarding the percentage of males as well as  with the cut⁃off value of 875.79,reflecting a sensitivity
                the levels of WBC,NEU,MON,ALT,CK,ESR,FIB,         of 72.97% and a specificity of 62.07%,indicating that
                D⁃D,baseline average dose of GC and anti⁃MDA5 anti⁃  SII was a moderately accurate predictor(Table 4).
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                bodies(Table 1).                                  2.4  Survival analysis of anti⁃MDA5 DM
                2.2  Risk factor analysis for RPILD and mortality     Among patients with anti⁃MDA5 DM,there was a
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                in anti⁃MDA5 DM                                   significant association between SII,NLR and RPILD
                    In the current study,we analyzed the risk factors  (P=0.001 and P < 0.001). When stratified by the opti⁃
                for developing RPILD and mortality in patients with anti  mal cut ⁃ off value of SII,the Kaplan ⁃ Meier survival
                ⁃ MDA5  +  DM,respectively. Univariate analysis re⁃  curve revealed that patients with SII>1 200.82 had a
                vealed that age and serum biomarkers(i.e.,NLR,PLR,  significantly lower incidence of non⁃RPILD within one

                SII,SIRI,and AISI)were positively correlated with the  year,compared to those with SII≤1 200.82(P=0.001,
                risk of developing RPILD[hazard ratio(HR)>1,P <   Figure 2A). Figure 2B showed that patients with an
                0.05,respectively]. A higher LMR was identified as a  NLR≤6.12 had a significantly lower incidence of non⁃
                protective factor against RPILD(Table 2). In the multi⁃  RPILD than those with an NLR>6.12(P < 0.001).
                variate Cox regression analysis,a high NLR remained   Furthermore,SII and NLR were found to be signifi⁃
                the strongest independent risk factor for RPILD[HR=  cantly associated with mortality(P < 0.001). Patients
                1.11,95% confidence interval(CI):1.03- 1.18,P=    with SII>875.79 had a significantly lower survival rate
                0.003](Table 2).                                  within one year,compared to those with SII≤875.79
                    To assess the risk of mortality,variables that  (Figure 3A). While,patients with NLR>6.12 had a
                showed significant differences in the univariate analysis  lower survival rate than those with NLR<6.12(Figure
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