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Abstract

Objectives:

There are inherent risks associated with intravenous thrombolysis (IVT) therapy in patients with acute ischemic stroke (AIS). The atherogenic index of plasma (AIP), defined as log (triglyceride [TG]/high-density lipoprotein cholesterol [HDL-C]), has recently been associated with the prognosis. We aimed to gauge AIP prognostic value in AIS patients receiving IVT.

Methods:

We retrospectively collected data from 183 AIS patients who underwent IVT. We grouped modified Rankin Scale scores of 0–2 and 3–6 as good and poor outcomes at 1 year, respectively. Multivariate logistic regression, receiver operating characteristic (ROC) curve and restricted cubic spline (RCS) analyses were used to investigate the underlying link between the AIP and 1-year functional outcomes.

Results:

In this study, 67 patients (36.6%) exhibited poor 1-year outcomes. An optimal AIP cut-off of 0.188 was used to divide the patients into low and high AIP levels. Our results showed that continuous AIP (odds ratio [OR] = 25.10, 95% confidence interval [CI]: 4.86–129.68, p < 0.001) was associated with poor 1-year outcome; when AIP was as a categorical variable, OR (95% CI) for the prognosis in the high AIP group was 27.86 (9.33–83.25) compared with the low AIP group. ROC analyses revealed that the area under the ROC curve for the AIP was 0.694 (0.603–0.785), with a sensitivity of 87.1% and a specificity of 61.2%. In the fully adjusted RCS, we found a positive but non-linear trend between the AIP and prognosis.

Conclusions:

High AIP may offer potential value as a novel target for predicting 1-year outcomes in patients receiving IVT.

1. Introduction

Acute ischemic stroke (AIS) is a debilitating and devastating disease, with a high global burden that is continuously increasing [1]. Although intravenous thrombolysis (IVT) with recombinant tissue-type plasminogen activator (rt-PA) has continued to occupy a pivotal position in the treatment of AIS, there are inherent risks associated with the process of IVT [2]. It is crucial to develop simple, non-invasive, and affordable biomarkers that could help assess prognosis and guide decision-making for eligible patients.

Atherosclerosis is a progressive disorder of arterial vessels. It is marked by the accumulation of lipids in the inner layer of the artery wall, increasing the incidence of AIS and cardiovascular disease (CVD) [3, 4]. Dyslipidemia is a key contributor to atherosclerosis, and is characterized by abnormal triglyceride (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C) levels [5, 6]. These findings have spurred further interest in the prognostic relevance of lipid profiles in AIS. The atherogenic index of plasma (AIP) is defined as log (TG/HDL-C) and is negatively correlated with LDL-C levels [7, 8]. Therefore, the AIP serves as a metric to assess the severity of dyslipidemia in patients. Notably, several studies have observed an association between AIP and AIS prognosis [9, 10]. High AIP was correlated with the 3-month clinical outcomes in patients with AIS. However, data regarding the long-term prognosis of patients undergoing IVT are scarce. Therefore, we aimed to further explore the ability of the AIP to predict 1-year functional outcomes in a population of AIS patients receiving IVT by building on previous research [11].

2. Materials and Methods
2.1 Study Design

To enhance data consistency and minimize loss to follow-up, 236 patients who underwent IVT and were admitted to Shanghai Fifth People’s Hospital (129 cases) and Taizhou People’s Hospital (107 cases) between January and December 2023 were enrolled between January and December 2023. Furthermore, all patients received standard statin therapy according to the guidelines [12]. Standardized telephone surveys were used to collect follow-up information.

The inclusion criteria for patients: (1) Aged 18 years. (2) Pretreatment modified Rankin Scale (mRS) score of 0–2. (3) Diagnosis of AIS was confirmed by head magnetic resonance imaging (MRI). The exclusion criteria: (1) Receiving bridging therapy; (2) Having hematologic diseases, active bleeding, severe heart, kidney, or liver failure, intracranial tumor; (3) being readmitted during the follow-up period; and (4) Incomplete or poor imaging/laboratory/follow-up information.

2.2 Data Collection

We collected demographic characteristics from the hospital records, including age, sex, body mass index (BMI), blood pressure, current smoking and drinking status, and medical history (including stroke or transient ischemic attack, coronary heart disease, atrial fibrillation, hypertension, and diabetes mellitus type 2). Neurological function was assessed using the NIH Stroke Scale (NIHSS) scores [13]. The Trial of ORG 10172 in Acute Stroke Treatment (TOAST) criteria were applied to categorize stroke subtypes [14].

2.3 Measurement of AIP

We gathered laboratory data, such as white blood cell (WBC), red blood cells (RBC), platelets (PLT), fasting plasma glucose (FPG), glycated haemoglobin A1c (HbA1c), TC, TG, HDL-C, and LDL-C. The AIP parameter was calculated as log(TG/HDL-C) [7].

2.4 Primary Outcomes

This study assessed the patients’ neurological function at 1 year. We classified mRS scores of 0–2 and 3–6 as indicating good and poor outcomes, respectively [15].

2.5 Statistical Analyses

All statistical analyses were performed using R software (version 4.4.1; R Foundation for Statistical Computing, Vienna, Austria). For categorical variables, the Chi-square test was applied. As for non-normally distributed continuous and ordinal variables, the Kruskal-Wallis test was employed. Multivariate logistic regression models were performed to explore the associations between continuous and categorical AIP and the 1-year functional outcomes. The best AIP cut-off value of 0.188 was determined corresponding the maximum Youden index (sensitivity – [1–specificity]) by the receiver operating characteristic (ROC) curve, with AIP divided into low and high levels. The crude model was a univariable analysis. Model 2 was adjusted for age, sex, BMI. In Model 3, we further adjusted for diastolic blood pressure (DBP), admission NIHSS, WBC, RBC, PLT, FPG, HbA1c, TC and LDL-C. In addition, we used ROC models to assess the predictive abilities of AIP and related lipid profiles. A fully adjusted restricted cubic spline (RCS) was applied to assess the associations of the continuous AIP with 1-year functional outcomes. Statistical significance was set at p < 0.05.

3. Results

After excluding a total of 53 patients (42 who received bridging therapy; 5 with concomitant aneurysm and/or arteriovenous malformation; 3 with intracranial tumor; 3 without complete data), 183 patients were finally selected. The flowchart is presented in Fig. 1.

Fig. 1.

Flowchart of the current study.

The characteristics of subjects are presented in Table 1. The included participants had a mean age of 67.16 years, and 65.03% were men. In total, 67 patients (36.6%) had poor outcomes, whereas 73.4% had good outcomes. The AIP was significantly higher in the poor outcome group (0.15 ± 0.34) than in the good outcome group (–0.03 ± 0.22) (p < 0.001). Compared with the good outcome group, the poor outcome group was more likely to be men and had significantly higher diastolic blood pressure (86.00 [79.00, 97.50] vs. 81.00 [73.50, 91.25], p = 0.007), admission NIHSS (5.00 [3.00, 9.00] vs. 4.00 [2.00, 7.00], p = 0.030), WBC (7.44 [5.66, 9.75] vs. 6.64 [5.44, 8.05], p = 0.026), RBC count (4.64 [4.22, 4.95] vs. 4.33 [3.98, 4.82], p = 0.017), FPG (6.20 [5.46, 8.00] vs. 5.61 [4.93, 6.88], p = 0.015), HbA1c (6.00 [5.60, 7.40] vs. 5.90 [5.50, 6.50], p = 0.046), TC (4.60 [3.90, 5.29] vs. 4.20 [3.27, 5.08], p = 0.027), TG (1.49 [1.02, 2.15] vs. 1.10 [0.80, 1.40], p < 0.001), LDL-C (2.91 [2.34, 3.38] vs. 2.61 [1.89, 3.29], p = 0.039), and lower HDL-C levels (0.97 [0.86, 1.25] vs. 1.21 [1.01, 1.36], p < 0.001).

Table 1. Baseline characteristics of included patients with acute ischemic stroke receiving intravenous thrombolysis according to 1-year functional outcomes.
Total Good outcome Poor outcome p value
(n = 116) (n = 67)
Demographics
Age, years 67.16 ± 12.24 67.31 ± 11.75 66.90 ± 13.15 0.432
Male, n (%) 119 (65.03) 67 (56.30) 52 (43.70) 0.007
Body Mass Index, kg/m2 23.31 (22.20, 25.60) 23.31 (22.20, 25.56) 23.26 (22.20, 25.54) 0.832
Clinical assessment
Systolic blood pressure, mmHg 150.00 (136.00, 163.00) 149.00 (136.00, 162.25) 150.00 (136.00, 163.00) 0.808
Diastolic blood pressure, mmHg 82.00 (75.00, 94.00) 81.00 (73.50, 91.25) 86.00 (79.00, 97.50) 0.007
Admission NIHSS 4.00 (3.00, 8.00) 4.00 (2.00, 7.00) 5.00 (3.00, 9.00) 0.030
Time to admission, hours 3.00 (2.00, 4.00) 3.00 (2.00, 4.00) 3.00 (2.00, 4.50) 0.910
Medical history, n (%)
Smoking 57 (31.15) 32 (56.14) 25 (43.86) 0.171
Drinking 37 (20.22) 24 (64.86) 13 (35.14) 0.835
Hypertension 121 (66.12) 78 (64.46) 43 (35.54) 0.673
Diabetes mellitus type 2 49 (26.78) 28 (57.14) 21 (42.86) 0.289
Coronary heart disease 11 (6.01) 6 (54.55) 5 (45.45) 0.760
Atrial fibrillation 28 (15.30) 19 (67.86) 9 (32.14) 0.594
Stroke or Transient ischemic attack 19 (10.38) 10 (8.62) 9 (13.43) 0.304
Stroke subtype, n (%) 0.444
Small-vessel 89 (48.63) 61 (68.54) 28 (31.46)
Large artery atherosclerosis 49 (26.78) 27 (55.10) 22 (44.90)
Cardioembolic 23 (12.57) 15 (65.22) 8 (34.78)
Undetermined or others 22 (12.02) 13 (59.09) 9 (40.91)
Laboratory data
White blood cell, 109/L 6.82 (5.50, 8.66) 6.64 (5.44, 8.05) 7.44 (5.66, 9.75) 0.026
Red blood cell, 109/L 4.40 (4.09, 4.85) 4.33 (3.98, 4.82) 4.64 (4.22, 4.95) 0.017
Platelet, 109/L 192.26 ± 59.06 187.17 ± 63.40 201.09 ± 49.89 0.125
Fasting plasma glucose, mmol/L 5.90 (4.99, 7.38) 5.61 (4.93, 6.88) 6.20 (5.46, 8.00) 0.015
HbA1c, (%) 5.90 (5.50, 6.70) 5.90 (5.50, 6.50) 6.00 (5.60, 7.40) 0.046
TC, mmol/L 4.40 (3.60, 5.17) 4.20 (3.27, 5.08) 4.60 (3.90, 5.29) 0.027
TG, mmol/L 1.15 (0.87, 1.68) 1.10 (0.80, 1.40) 1.49 (1.02, 2.15) <0.001
HDL-C, mmol/L 1.13 (0.93, 1.34) 1.21 (1.01, 1.36) 0.97 (0.86, 1.25) <0.001
LDL-C, mmol/L 2.78 (2.05, 3.35) 2.61 (1.89, 3.29) 2.91 (2.34, 3.38) 0.039
Atherogenic index of plasma 0.03 ± 0.28 –0.03 ± 0.22 0.15 ± 0.34 <0.001

Normally distributed continuous variables are presented as means ± standard deviation, and continuous variables without a normal distribution are presented as medians (interquartile ranges). Categorical variables are presented as counts (percentages).

NIHSS, National Institutes of Health Stroke Scale; HbA1c, glycated haemoglobin A1c; TC, total cholesterol; TG, triglyceride; HDL-C, high-density lipoprotein cholesterol; LDL-C, low-density lipoprotein cholesterol.

In the fully adjusted regression models, AIP as a continuous variable (odds ratio [OR]: 25.10; 95% confidence interval [CI]: 4.86–129.68) was associated with 1-year poor outcomes. When AIP was set as a categorical variable, ORs (95% CI) with the high AIP were 27.86 (9.33–83.25) for the prognosis compared with the low AIP (Table 2). ROC analyses showed that the best cut-off AIP value was 0.188. The sensitivity was 87.1%, the specificity was 61.2%, and the area under the ROC curve (AUC) of the AIP was 0.694 (0.603–0.785), which was preferable to other related lipid profiles (0.598 for TC, 0.663 for TG, 0.656 for HDL-C, and 0.592 for LDL-C) (Table 3 and Fig. 2). We also applied adjusted RCS plots to reveal the potential dose-manner associations between the AIP and poor 1-year outcome (Fig. 3). Here, we observed that high AIP was associated with a higher risk of 1-year outcomes, and a positive but non-linear trend was observed.

Table 2. Association of AIP with 1-yaer functional outcomes in patients with acute ischemic stroke receiving intravenous thrombolysis.
Model 1 Model 2 Model 3
OR (95% CI) p value OR (95% CI) p value OR (95% CI) p value
AIP 12.85 (3.7044.58) <0.001 15.06 (3.9058.15) <0.001 25.10 (4.86129.68) <0.001
Low 1.00 (Reference) 1.00 (Reference) 1.00 (Reference)
High 10.62 (5.1122.07) <0.001 14.32 (6.2332.93) <0.001 27.86 (9.3383.25) <0.001

Multivariate logistic regression results are presented as ORs and 95% CIs.

Model 1: Crude.

Model 2: Adjusted for age, sex, BMI.

Model 3: Adjusted for age, sex, BMI, and DBP, admission NIHSS, WBC, RBC, PLT, FPG, HbA1c, TC, LDL-C.

OR, Odds Ratio; CI, Confidence Interval; AIP, atherogenic index of plasma.

Table 3. Abilities of AIP, TC, TG, HDL-C and LDL-C for predicting 1-year functional outcomes in patients with acute ischemic stroke receiving intravenous thrombolysis.
AUC 95% CI Sensitivity Specificity p value
AIP 0.694 (0.603–0.785) 0.871 0.612 <0.001
TC 0.598 (0.516–0.681) 0.250 0.955 0.053
TG 0.663 (0.576–0.750) 0.784 0.537 <0.001
HDL-C 0.656 (0.567–0.746) 0.707 0.642 0.008
LDL-C 0.592 (0.509–0.674) 0.293 0.925 0.065

Receiver operating characteristic curve results are presented as AUC with 95% CI, sensitivity, and specificity.

AUC, Area Under the Curve; CI, Confidence Interval; AIP, atherogenic index of plasma.

Fig. 2.

Receiver operating characteristic curve of AIP for predicting 1-year functional outcome in patients with acute ischemic stroke receiving intravenous thrombolysis.

Fig. 3.

Association between AIP and 1-year functional outcome in patients with acute ischemic stroke receiving intravenous thrombolysis using restricted cubic spline analysis.

4. Discussion

This is the first research focusing on AIP-related differences in the prognosis of AIS patients receiving IVT. High AIP was associated with poor 1-year functional outcomes. Additionally, we observed a positive but non-linear relationship between AIP and prognosis. These findings underscore the importance and need to consider the AIP levels when making medical decisions for AIS patients, consistent with the growing data suggesting that atherosclerosis plays a crucial role in AIS [16].

Atherosclerosis is the key cause of AIS and CVD [3, 4, 5, 6]. Thus, numerous lipid profiles have been used to evaluate the functional outcomes of AIS. However, traditional single index (TC, TG, HDL-C, LDL-C) as the evaluation of AIS was still limited and exhibited low predictive value. Small dense LDL-C (sdLDL-C) is significantly high associated with atherosclerosis, as is the case with AIS [17]. Furthermore, sdLDL-C detection is both difficult and costly, creating a need for an inexpensive and reliable tool to assess the degree of atherosclerosis in given patients. The AIP is a routine index that can indirectly reflect sdLDL-C levels [18]. Importantly, AIP can be easily computed using TG and HDL-C values, making it an inexpensive and reliable tool. The prognostic ability of the AIP has been suggested in CVD and the instability of carotid plaque [19, 20]. A 2024 study confirmed the associations of AIP with the 3-month outcomes of AIS [21]. However, no studies have examined the potential relationship between the AIP and long-term prognosis of AIS patients, regardless of receiving IVT. Our findings could extend the explanation, as we revealed that high AIP was linked to the 1-year poor outcome, with a positive but non-linear trend seen. When patients had high AIP, they had a higher risk of 1-year poor outcome compared with those with low AIP. Our study suggests that high AIP may offer greater predictive value than other related conventional lipid profiles. Given its ease of measurement and high predictive value, the AIP serves as an ideal tool for assessing patients with AIS, helping to better predict functional outcomes before IVT.

Despite the unclear mechanisms, several possible explanations may be proposed. High TG levels have been implicated in vascular subclinical atherosclerosis and might intensify the inflammatory reactions in both smooth muscle cells and vascular endothelial cells [22]. Conversely, HDL-C could exert multiple vasoprotective effects, including reducing apoptosis, mitigating inflammation, and protecting against oxidative stress [23]. Accordingly, the fact that AIP values offer simultaneous information obtained from patients’ TG and HDL-C levels could reflect pro-inflammatory and atherosclerotic effects modulated by high TG levels and the reduced anti-inflammatory HDL-C responses. Participants with high AIP tended to have higher BMI and HbA1c levels and were more likely to be smokers or drinkers, all of which led to AIS.

Our study, however, has several limitations. As a two-center, single-year investigation, its relatively small sample size may have limited the statistical power. Moreover, we did not assess the dynamic changes in AIP during hospital stay, an aspect that warrants further investigation in future studies.

5. Conclusions

In summary, high AIP was associated with poor 1-year functional outcomes in AIS patients receiving IVT, with a positive but non-linear relationship between AIP and prognosis. Future larger-scale studies are needed to clarify its clinical application.

Availability of Data and Materials

The datasets are available from the corresponding author on reasonable request.

Author Contributions

RS: conceptualization, investigation, formal analysis, writing. ZW: designing the research study, performing the research, writing. Both authors read and approved the final manuscript. Both authors have participated sufficiently in the work and agreed to be accountable for all aspects of the work.

Ethics Approval and Consent to Participate

This study was approved by the ethics committee of Taizhou Clinical Medical School of Nanjing Medical University (KY2024-124-01) and the Shanghai Fifth People’s Hospital (2024-096). Informed consent was waived because of the retrospective nature. The study was carried out in accordance with the guidelines of the Declaration of Helsinki.

Acknowledgment

Not applicable.

Funding

This study was funded by Minhang District natural science research project funding (2022MHZ039).

Conflict of Interest

The authors declare no conflict of interest.

References

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