Abstract
Absent in melanoma 2 (AIM2) is implicated in neuroinflammation. Here, we explored the prognostic significance of serum AIM2 in human aneurysmal subarachnoid hemorrhage (aSAH). We conducted a consecutive enrollment of 127 patients, 56 of whom agreed with blood-drawings not only at admission but also at days 1, 2, 3, 5, 7 and 10 days after aSAH. Serum AIM2 levels of patients and 56 healthy controls were measured. Disease severity was assessed using the modified Fisher scale (mFisher) and World Federation of Neurological Surgeons Scale (WFNS). Neurological outcome at poststroke 90 days was evaluated via the modified Rankin Scale (mRS). Univariate analysis and multivariate analysis were sequentially done to ascertain relationship between serum AIM2 levels, severity, delayed cerebral ischemia (DCI) and 90-day poor prognosis (mRS scores of 3–6). Patients, in comparison to controls, had a significant elevation of serum AIM2 levels at admission and at days 1, 2, 3, 5, 7 and 10 days after aSAH, with the highest levels at days 1, 2, 3 and 5. AIM2 levels were independently correlated with WFNS scores and mFisher scores. Significantly higher serum AIM2 levels were detected in patients with a poor prognosis than in those with a good prognosis, as well as in patients with DCI than in those without DCI. Moreover, serum AIM2 levels independently predicted a poor prognosis and DCI, and were linearly correlated with their risks. Using subgroup analysis, there were no significant interactions between serum AIM2 levels and age, gender, hypertension and so on. There were substantially high predictive abilities of serum AIM2 for poor prognosis and DCI under the receiver operating characteristic curve. The combination models of DCI and poor prognosis, in which serum AIM2, WFNS scores and mFisher scores were incorporated, showed higher discriminatory efficiencies than anyone of the preceding three variables. Moreover, the models are delineated using the nomogram, and performed well under the calibration curve and decision curve. Serum AIM2 levels, with a substantial enhancement during early phase after aSAH, are closely related to bleeding severity, poor 90-day prognosis and DCI of patients, substantializing serum AIM2 as a potential prognostic biomarker of aSAH.
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Introduction
Non-traumatic subarachnoid hemorrhage (SAH) is a life-threatening and highly fatal neurological condition, with aneurysmal rupture accounting for approximately 85% of such cases1. Aneurysmal SAH (aSAH) is characterized by a rapid onset, high disability and high mortality rate. Early brain injury involves inflammatory reaction, oxidative stress and apoptosis, and has been believably accepted as a very important mechanism, which leads to neuronal injury2,3. One of the most common and serious complications is delayed cerebral ischemia (DCI), which may be mainly caused by cerebral vasospasm and increases the risk of poor prognosis in patients with aSAH4. It is a crucial step to predict DCI and even a poor prognosis during the clinical management of aSAH. Biomarkers can assist in assessing severity and predicting prognosis. In recent decades, measurements of circulating biomarkers, such as complement component 1q, A20, S100B and copeptin, have been increasingly noted with respect to their prognostic predictive values in aSAH5,6,7,8.
Inflammasomes are a group of multimeric protein complexes that can protect host against infectious agents and physiological aberration9. Absent in melanoma 2 (AIM2) is an inflammasome receptor that can be activated in response to double-stranded DNA10. AIM2 engages caspase-1 to catalyze proteolytic cleavage of pro-interleukin-1β and pro-interleukin-18 and drive pyroptosis, thereby inducing inflammation and cellular death11,12. AIM2 is mainly expressed in glial cells13. Its expressions could be greatly up-regulated in animal brain tissues at some pathological situations, such as Alzheimer’s disease, autoimmune encephalomyelitis, ischemic stroke and SAH13,14,15,16. AIM2 could damage neurons during ischemic and hemorrhagic injury via increasing neuroinflammation and oxidative stress after experimental SAH, hypoxic-ischemic brain injury, middle cerebral artery occlusion and traumatic brain injury17,18,19,20. Noteworthily, acute ischemic stroke patients had significantly higher levels of plasma AIM2 than healthy controls; moreover, plasma AIM2 levels were intimately correlated with severity and 90-day poor prognosis after stroke21, indicating that AIM2 may be a biomarker of acute brain injury. Here, serum AIM2 was measured and its prognostic role was investigated in aSAH.
Methods and materials
Participants
In this prospective observational study, we consecutively recruited patients with aSAH at the Affiliated Hangzhou First People’s Hospital, Westlake University School of Medicine and the Sixth Affiliated Hospital of Wenzhou Medical University between April 2020 and December 2022. Our study included patients with first-time nontraumatic SAH. We specified the following eligibility criteria: (1) patients must be 18 years of age or older; (2) SAH was verified using head computed tomography (CT) scans; (3) aneurysm diagnosis must be confirmed through computed tomography angiography (CTA) or digital subtraction angiography (DSA); (4) patients should be admitted to the hospital within 24 h of symptom onset; (5) ruptured intracranial aneurysms should be repaired within 48 h of admission through surgical clipping or interventional embolization. Exclusion criteria included: (1) severe diseases in other organs; (2) previous neurological diseases, such as ischemic or hemorrhagic stroke, myasthenia gravis, severe traumatic brain injury, moyamoya disease, arteriovenous malformation, or intracranial neoplasm; (3) suspected pseudoaneurysm or aneurysm rebleeding; (4) loss to follow-up, insufficient information, rejection to participation, or missing samples. The study was performed in accordance with the Declaration of Helsinki and its amends. The study protocol was approved by the ethical committees at the Affiliated Hangzhou First People's Hospital, Westlake University School of Medicine (No. 058-01) and the Sixth Affiliated Hospital of Wenzhou Medical University (No. 2020-001). And written informed consent was obtained from the patients' relatives and controls themselves.
Variables
The data we collected included (1) demographical information, such as age and gender; (2) the presence of underlying chronic diseases, such as hypertension, diabetes and hyperlipidemia; (3) medications, such as antiplatelet agents, anticoagulants and hormones; (4) unhealthy lifestyle habits, such as cigarette smoking and alcohol consumption. To assess the patient's health status and determine appropriate treatment options, non-invasive techniques were used to measure vital signs, such as blood pressure, respiratory rate, heart rate and blood oxygen saturation. The modified Fisher (mFisher) scale and the World Federation of Neurosurgical Societies (WFNS) scale, which provide standardized ways to assess and classify the severity of SAH, were employed as the two indicators for evaluating the radiological and clinical severity of the hemorrhage. CT scans were made to identify intraventricular hemorrhage and acute hydrocephalus, and further head CTA or DSA was performed to determine the location, size and shape of intracranial aneurysms. When determining whether neurosurgical clipping or endovascular intervention was selected as a treatment option for securing aneurysms, the following factors were cautiously taken into consideration, including aneurysm characteristics, patient preferences, overall patient conditions, presence of intracerebral bleeding, intracranial pressure, etc.
The following specific criteria were referred to assess the occurrence of DCI: (1) clinical deterioration (such as new focal deficit, decrease in level of consciousness, or both), and/or (2) detection of new infarction on head CT scans that was not visible on admission or in the early postoperative period and cannot be attributed to any other cause through clinical evaluation, brain imaging, and appropriate laboratory tests22. Follow-up on neurologic function was done until 90 days after the injury, and the prognosis was evaluated using the modified Rankin Scale (mRS). The scores of 3–6 on the mRS indicated a poor prognosis23.
Immune analysis
At admission, blood samples were taken from patients and some routine laboratory parameters (e.g., blood white cell count, platelet count, hemoglobin level, and blood glucose) were measured by conventional methods. For the sake of measuring serum AIM2 levels, blood samples of controls were acquired at their entry into study; all patients underwent blood-collections at admission and a portion of patients had blood-obtainments at other multiple time-points, namely, at days 1, 3, 5, 7 and 10. To measure serum AIM2 levels, venous blood samples were spun for 15 min at 3000×g and serum was isolated. And then, an aliquot of serum sample was taken and stored promptly at − 80 °C until testing. Then, serum AIM2 levels were quantified in duplicate using an enzyme-linked immunosorbent assay kit (Shanghai Jianglai Biotechnology Co., Ltd, China; Catalogue number, JL49566) according to the manufacturer's instructions. The detection range of this kit was from 0.156 ng/ml to 10 pg/ml, with intra-assay precision of ≤ 10% and inter-assay precision of ≤ 10%. The final analysis was performed using the average value of the two measurements. All measurements were carried out by the same technician, who was inaccessible to clinical materials.
Statistical analysis
The data were analyzed using the SPSS 25.0 (BMI Software Inc., USA). Graphs were drawn using the GraphPad Prism 9.0 (GraphPad Software, Inc., Boston, MA, USA) and R software (version 4.2.4; https://www.r-project.org). Qualitative variables were expressed as frequency (percentage), and normally and non-normally distributed continuous variables were expressed as mean (standard deviation, SD) and median (interquartile range) respectively. The comparisons of various variables between the two groups were performed using the Chi-square test or Fisher's exact test for qualitative data, and the Mann–Whitney U test or independent t-test for quantitative data. The Kruskal–Wallis test was used for multiple-group comparisons of quantitative data. The Spearman correlation coefficient was used to calculate the bivariate correlation between serum AIM2 levels and other variables, such as WFNS score and mFisher score. After adjusting for other confounding factors which were significant on univariate analysis (P < 0.05), multivariable linear regression correlation analysis was performed to determine the variables, which were independently correlated with serum AIM2 levels. To determine the factors, which were independently associated with 90-day adverse prognosis and DCI, the binary logistic regression model was established, in which the significant variables on the univariate analysis (P < 0.05) were included. The results were expressed as odds ratios (ORs) and 95% confidence intervals (CIs). Receiver operating characteristic (ROC) curves were used to study the predictive value of serum AIM2 levels for DCI and 90-day adverse prognosis in patients. The area under the curve (AUC) was calculated. The Youden's J method was applied to identify the optimal threshold of serum AIM2 levels to further distinguish patients at risk of DCI or 90-day adverse prognosis, with corresponding sensitivity and specificity values. The independent predictors of DCI or adverse prognosis were incorporated to form prediction model. And the model was described using the nomogram, and was assessed using the calibration curve, decision curve and ROC curve. A two-tailed P-value less than 0.05 was considered statistically significant.
Results
Patient selection and characteristics
In this prospective cohort study, a total of 175 patients with first-ever SAH underwent initial evaluation. Among them, 48 patients were excluded because of the reasons outlined in Fig. 1. Of the finally enrolled 127 patients, 56 consented for blood-collection at multiple time points and constituted a special group for uncovering dynamic change of serum AIM2 levels after stroke. Among these 56 patients, 29 were females and 27 were males, 16 smoked cigarettes and 12 drank alcohol. Their mean age was 53.4 years (SD, 10.2 years). A total of 56 healthy controls were recruited. Among these 56 healthy controls, 34 were females and 22 were males, 13 smoked cigarettes and 15 drank alcohol. Their mean age was 51.7 years (SD, 10.6 years). There were no significant differences in age, sex ratio, smoking and drinking between those 56 aSAH patients and 56 healthy controls (all P > 0.05). As shown in Table 1. There were no significant differences in clinical, radiological and biochemical indexes between all 127 patients and those 56 patients (all P > 0.05).
Temporal change of serum AIM2 levels after aSAH and its correlation with severity
Compared with the control group, the serum AIM2 levels of those 56 patients increased significantly on admission, the highest levels appeared at days 1, 2, 3 and 5, and the serum AIM2 levels decreased slowly at day 7 until day 10. Serum AIM2 levels of patients were substantially higher during 10 days than those of controls (P < 0.001; Fig. 2). Serum AIM2 levels of all 127 patients, ranging from 0.48 to 2.88 ng/ml with a median value of 1.59 ng/ml (25th–75th percentiles, 1.17–2.16 ng/ml), were equivalent to those of those 56 patients (P > 0.05). Also, there were non-statistically significant differences in terms of serum AIM2 levels between all 127 patients and those 56 patients (P > 0.05). Serum AIM2 levels were substantially positively correlated with WFNS scores (P < 0.001; Fig. 3A) and mFisher scores (P < 0.001; Fig. 3B), as well as were significantly increased in order of WFNS scores (P < 0.001; Fig. 3C) and mFisher scores (P < 0.001; Fig. 3D). In Table 2, serum AIM2 levels showed a close correlation with other variables, including intraventricular bleeding, blood glucose levels and serum C-reactive protein levels (all P < 0.05). When adding the above variables to the multivariate linear regression model, serum AIM2 levels were independently associated with WFNS scores (β, 0.125; 95% CI, 0.030–0.220; VIF, 0.747; P = 0.010) and mFisher scores (β, 0.124; 95% CI, 0.006–0.242; VIF, 0.666; P = 0.039).
Relationship between serum AIM2 levels and 90-day functional outcome after aSAH
Among those patients who consented for blood-collections at multiple time-points, cases with development of poor prognosis (mRS scores of 3–6) accounted for 42.9% (24/56). In this portion of patients, serum AIM2 levels at days 1, 2, 3, 5, 7 and 10 days after aSAH had AUCs at 0.734 (95% CI, 0.628–0.883), 0.778 (95% CI, 0.658–0.902), 0.750 (95% CI, 0.602–0.865), 0.710 (95% CI, 0.559–0.833), 0.668 (95% CI, 0.515–0.798) and 0.653 (95% CI, 0.500–0.786) respectively. As compared to those at admission (AUC, 0.682; 95% CI, 0.530–0.810), they had non-statistically significant AUCs for predicting 90-day poor prognosis (all P > 0.05).
Among all 127 patients, 50 patients had a poor prognosis at 90 days after the onset of aSAH. Serum AIM2 levels were significantly positively correlated with mRS scores (P < 0.001; Fig. 4A), were substantially elevated in order of mRS scores (P < 0.001; Fig. 4B). The concentration of serum AIM2 in patients with poor prognosis was significantly higher than that in patients with good prognosis. (P < 0.001; Fig. 5A). Under the ROC curve, associated criterion was 1.61 ng/ml using the Youden method. The sensitivity of serum AIM2 level to predict the risk of 90-day poor prognosis was 78.0%, and the specificity was 72.3% (Fig. 5B). In addition, restricted cubic spline analysis showed a linear association of serum AIM2 levels with the risk of poor prognosis at 90 days (Fig. 6, P > 0.05).
As listed in Table 3, as opposed to patients with good prognosis, those presenting whit poor prognosis had significantly higher proportion of serum AIM2 levels (P < 0.001), displayed substantially higher percentage of intraventricular hemorrhage (P < 0.05), and tended to exhibit markedly higher blood glucose levels (P < 0.05), serum C-reactive protein levels (P < 0.05), WFNS scores (P < 0.001) and mFisher scores (P < 0.001). All the abovementioned significant variables were forced into the multivariate model, and it was found that WFNS score (OR, 1.591; 95% CI, 1.022–2.493; P = 0.040), mFisher score (OR, 1.822; 95% CI, 1.063–3.134; P = 0.030) and serum AIM2 levels (OR, 2.389; 95% CI, 1.079–5.290; P = 0.032) independently predicted the occurrence of poor prognosis at 90 days after hemorrhagic stroke. We further analyzed interactions of serum AIM2 levels on age, sex, hypertension, smoking and drinking, and found that no significantly statistical interactions existed (all P > 0.05; Fig. 7).
We established a model of serum AIM2 combined with WFNS score and mFisher score. The model was visually described using a nomogram (Fig. 8). Using calibration curve, the model was comparatively stable (Fig. 9). Using decision curve analysis, the model had comparatively high benefit (Fig. 10). In Fig. 11, serum AIM2 levels effectively distinguished patients at risk of poor prognosis, with AUC > 0.75; the predictive ability of serum AIM2 level was similar to those of mFisher score (P > 0.05) and WFNS score (P > 0.05); and the model had significantly higher predictive capability than that of WFNS score, mFisher score and serum AIM2 level alone (all P < 0.05).
Relationship between serum AIM2 levels and DCI after aSAH
As for predictive ability for DCI, AUCs of serum AIM2 levels at 1, 2, 3, 5, 7 and 10 days after stroke were 0.758 (0.634–0.887), 0.762 (0.615–0.874), 0.770 (0.588–0.854), 0.682 (0.530–0.810), 0.665 (0.513–0.796) and 0.661 (0.508–0.792) respectively. Their AUCs were equivalent to that of admission serum AIM2 levels (AUC, 0.719; 95% CI, 0.569–0.840) in this group of 56 patients with aSAH (all P > 0.05).
Among all 127 patients, a total of 38 patients suffered from DCI. Serum AIM2 levels in patients with DCI was significantly higher than that in patients without DCI (Fig. 12A). The sensitivity of serum AIM2 levels to predict the occurrence of DCI was 73.7% and the specificity was 78.7%. Using the Youden method, the associated criterion was 1.89 ng/ml (Fig. 12B). The restricted cubic spline analysis showed a linear association between serum AIM2 levels and DCI risk (Fig. 13, P > 0.05).
In Table 4, in contrast to patients without development of DCI, those with suffering of DCI had significantly elevated serum AIM2 levels (P < 0.001), as well as exhibited substantially raised blood glucose levels (P < 0.01), intraventricular bleeding (P < 0.05), WFNS scores (P < 0.001) and modified Fisher scores (P < 0.001). Using multivariate analysis, WFNS score (OR, 1.693; 95% CI, 1.043–2.741; P = 0.033), mFisher score (OR, 2.109; 95% CI, 1.144–3.873; P = 0.017) and serum AIM2 levels (OR, 2.640; 95% CI, 1.101–6.329; P = 0.030) were independently associated with DCI risk after aSAH. The subgroup analysis of serum AIM2 level and DCI showed that there were no significantly different interactions between serum AIM2 levels and other variables, such as age, gender, hypertension, smoking, and alcohol drinking (Fig. 14).
We also established a model of serum AIM2 combined with WFNS score and mFisher score. The model, which was delineated using nomogram (Fig. 15), was of relative stability (Fig. 16). The prediction models had comparatively high benefit by using decision curve analysis (Fig. 17). As outlined in Fig. 18, serum AIM2 levels were effective in predicting the occurrence of DCI after aSAH (AUC > 0.75); interestingly, serum AIM2 levels had similar predictive ability compared with the mFisher score (P > 0.05) and WFNS score (P > 0.05); combination model, in which serum AIM2, WFNS score and mFisher score were merged, had AUC at 0.849; and the predictive power of the combined model was found to be significantly higher than that of the WFNS score, mFisher score and serum AIM2 levels alone (all P < 0.05).
Discussion
To the best of our knowledge, it is unclear regarding circulating levels of AIM2 in aSAH. In this study, serum AIM2 levels of aSAH patients were significantly higher than those of healthy controls. Alternatively, in clinical practice, WFNS and mFisher scores were conventionally utilized to evaluate disease severity, and predict functional outcome and DCI after aSAH. Currently, serum AIM2 levels were significantly positively correlated with mFisher scores and WFNS scores. Also, besides WFNS scores and mFisher scores, serum AIM2 levels were independently related to the occurrence of DCI and poor prognosis 90 days after aSAH. In addition, the predictive power of serum AIM2 levels for DCI and poor prognosis resembled those of mFisher scores and WFNS scores; moreover, the combination model, in which serum AIM2, WFNS scores and mFisher scores, displayed higher predictive efficiency for DIC or poor prognosis. To sum up, the increase of serum AIM2 level may be closely related to the severity of aSAH, and be independently related to functional prognosis and DCI, suggesting that serum AIM2 may be a potential biomarker for the prognosis of aSAH.
DCI, one of the most common and severe complications of aSAH, is the major cause of morbidity and mortality in patients who survive primary treatment of ruptured intracranial aneurysms24. The pathological processes of DCI involve cerebrovascular spasm, microcirculation contraction, microthrombosis, diffuse cortical ischemia and delayed apoptosis, which are all related to inflammation and oxidative stress after aSAH25,26,27. On the other hand, inflammation is the pivotal mechanisms, which are implicated in early brain injury following aSAH28. So, some biomarkers, which are pertinent to inflammation, may be promising predictive indicators of functional outcomes and DCI.
AIM2 is a member of the interferon-induced HIN-200 family of proteins and is a DNA receptor29. It is mainly localized in the cytoplasm and plays an important role in a number of inflammation-associated diseases30. AIM2 forms a functional inflammatory vesicle in cortical neurons, which is responsible for sensing intracellular damage caused by exogenous or endogenous sources29,30. It can recognize exogenous dsDNA and induce cystatinase-1 activation and release of mature inteuleukin-1beta31. So, AIM2 inflammasomes may be activated specifically in response to DNA damage. In the central nervous system, there are high expressions of AIM2 inflammasomal proteins, which may be implicated in cell death in neurons32.
In AIM2 knockout mice with vascular dementia, interleukin-1beta and -18 productions were significantly diminished and cognitive impairment was improved greatly17. Also, knockout of AIM2 obviously lessened blood–brain barrier destruction in mice after cerebral vascular occlusion18,19. Similarly, AIM2 knockout markedly reduced neuronal pyroptosis after subarachnoid hemorrhage and therefore decreased neurological impairment of rats20. AIM2 may be involved in damaged blood–brain barrier after traumatic brain injury33. Hence, it is believably accepted that AIM2 may be a detrimental factor in acute brain injury. AIM2 could be tremendously generated from brain tissues, mainly in glial cells after brain injury34. In our study, a portion of patients offered continuous blood drawings. These patients had similar demographic, clinical and biochemical data, as compared to the total patient population, indicating that these patients should represent the whole cohort of patients with aSAH. Noteworthily, our study showed that serum AIM2 levels in patients were significantly higher than those in healthy controls, and this increase lasted until at least 10 days after the onset of stroke. Therefore, it is postulated that blood AIM2 levels may be actually elevated after aSAH and moreover, AIM2 in blood may be at least partially derived from the damaged brain tissue after aSAH.
In the current study, as opposed to serum AIM2 levels at admission, those at days 1, 2, 3, 5, 7 and 10 had similar DCI and prognosis predictive abilities in terms of AUC. For the sake of investigating relationship between serum AIM2 levels and illness severity in addition to DCI and prognosis, serum AIM2 levels at admission were analyzed. Using multivariate analysis, serum AIM2 levels were independently correlated with WFNS score and mFisher score; moreover, the levels independently predicted DCI and poor prognosis. In our study, linear correlations and subgroup analyses were implemented. Presumably, serum AIM2 levels were linearly correlated with risks of DCI and poor prognosis. In addition, no interactions were found between serum AIM2 levels and other conventional variables, such as age, gender, hypertension and alcohol consumption. Overall, the preceding results are strongly supportive of the notion that serum AIM2 at admission may serve as a potential prognostic biochemical marker of aSAH.
As for the predictive capability, serum AIM2 levels efficiently differentiated between patients with DCI and those without, as well as between patients with poor prognosis and those with good prognosis. Intriguingly, the predictive values of serum AIM2 levels for the two prognostic indicators resemble those of WFNS score and mFisher score. Furthermore, the combination of serum AIM2 levels with WFNS score and mFisher score as a model, showed significantly improved prognostic ability, as compared with WFNS score and mFisher score alone. The two models were graphically represented. Theoretical calibration curves and decision curves were then created and subsequently it was verified that the models manifested well, with high stability and clinical benefits. Hence, it should be admitted that determination of serum AIM2 may assist to increase clinical prognostic ability of aSAH.
This study has certain limitations. First, we measured the serum AIM2 levels of patients at multiple time points and compared them with those of healthy volunteers, finding that AIM2 may have scientific value for the prognosis of aSAH and DCI patients. However, we acknowledge that the number of patients agreeing to undergo multiple-time-point blood-collection was limited, so this conclusion needs to be validated in studies with a larger sample size. Second, the prognosis and DCI of aSAH are closely related to the overall condition of the body35. aSAH not only damages brain tissue but also triggers systemic oxidative stress and inflammatory reactions36. AIM2 can promote the production of inflammatory factors interleukin-1β and interleukin-18 and cause intracellular damage when specifically activated37. Therefore, AIM2 may not only potentially harm the central nervous system but also have potential effects on the peripheral system38. Current research indicates that serum AIM2 levels are closely related to the 90-day prognosis and DCI of aSAH, and serum AIM2 may also be a biological marker that accurately reflects systemic inflammatory responses, but this requires further research for validation.
Conclusions
To the best of our knowledge, this is a first series for unveiling the prognostic role of serum AIM2 in aSAH. Our main findings are that serum AIM2 levels are independently related to hemorrhage severity, DCI and 90-day functional outcome after aSAH; moreover, serum AIM2 exhibits significantly effective predictive ability for DCI and poor prognosis at 90 days following aSAH. Taken together, serum AIM2 may be a potential biomarker for assessing hemorrhage severity and predicting DCI and 90-day functional outcome after aSAH.
Data availability
The datasets generated and/or analyzed during the current study are not publicly available because they are personal data, but are available from the corresponding author upon reasonable request.
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Acknowledgements
We gratefully thank all study participants, their relatives and the staff at the recruitment centers for their invaluable contributions.
Funding
This work is financially supported by grants from Key Research and Development Projects of Zhejiang Province (2020C03071) and the Construction Fund of Medical Key Disciplines of Hangzhou (OO20200485, OO20200055).
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Ziyin Chen, Dingbo Yang and Shengdong Zou: Conceptualization, Methodology, Writing-Reviewing and Editing. Quan Du and Xiaoqiao Dong: Data curation, Writing-Original draft preparation. Hao Shan and Jin Liu: Visualization, Investigation. Da Tian and Xiaoyu Wu: Supervision, Software, Validation. All authors reviewed the manuscript.
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Chen, Z., Zou, S., Shan, H. et al. Longitudinal change of serum AIM2 levels after aneurysmal subarachnoid hemorrhage and its prognostic significance: a two-center prospective cohort study. Sci Rep 14, 10430 (2024). https://doi.org/10.1038/s41598-024-61185-1
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DOI: https://doi.org/10.1038/s41598-024-61185-1
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