Skip to main content
Download PDF

High glycated albumin is associated with early neurological deterioration in patients with acute ischemic stroke

BMC Neurology volume 24, Article number: 278 (2024) Cite this article

Abstract

Background

Glycated albumin (GA) is an indicator of glycemic variability over the past 2–4 weeks and has suitable characteristics for predicting the prognosis of ischemic stroke during the acute phase. This study evaluated the association between early neurological deterioration (END) and GA values in patients with acute ischemic stroke (AIS).

Methods

We assessed consecutive patients with AIS between 2022 and 2023 at two large medical centers in Korea. END was defined as an increase of ≥ 2 in the total National Institutes of Health Stroke Scale (NIHSS) score or ≥ 1 in the motor NIHSS score within the first 72 h of admission. We evaluated various glycemic parameters including fasting glucose (mg/dL), hemoglobin A1c (%), and GA (%).

Results

In total, 531 patients with AIS were evaluated (median age: 69 years, male sex: 66.3%). In the multivariable logistic regression analysis, GA value was positively associated with END (adjusted odds ratio [aOR] = 3.24, 95% confidence interval [CI]: 1.10–9.50). Initial NIHSS score (aOR = 1.04, 95% CI: 1.01–1.08) and thrombolytic therapy (aOR = 2.06, 95% CI: 1.14–3.73) were also associated with END. In a comparison of the predictive power of glycemic parameters for END, GA showed a higher area under the curve value on the receiver operating characteristic curve than fasting glucose and hemoglobin A1c.

Conclusions

High GA values were associated with END in patients with AIS. Furthermore, GA was a better predictor of END than fasting glucose or hemoglobin A1c.

Peer Review reports

Background

Diabetes and hyperglycemia are well-known risk factors for ischemic stroke [1]. Elevated blood glucose levels not only increase the risk of ischemic stroke but also have a significant impact on both short- and long-term outcomes [2,3,4]. European and US guidelines recommend glucose control within appropriate levels in patients with ischemic stroke and suggest plasma glucose and hemoglobin A1c as monitoring indicators for this purpose [5,6,7]. However, plasma glucose is greatly influenced by diet, type and timing of glucose-lowering agents, and accompanying medical comorbidities. In addition, it can temporarily increase as an acute-phase reactant after a stroke [8, 9]. In contrast, hemoglobin A1c is a relatively stable reflector of glycemic status [10]. However, since hemoglobin A1c reflects data from the past 2–3 months, its usefulness as an indicator of prognosis or treatment response during the acute phase of ischemic stroke is limited.

The glycated albumin (GA) level is an indicator of short-term glycemic variability [11]. GA reflects the glycemic variability over the past 2–4 weeks due to the rapid turnover of albumin and its high glycation rate [12,13,14]. Recently, glycemic variability has been recognized to play an important role in the development of microvascular- and macrovascular complications in diabetic patients, as much as chronic hyperglycemia [11, 15]. Therefore, GA is considered a useful indicator of glycemic control. Furthermore, GA has the advantage that it is not overly affected by external factors as much as plasma glucose and can be used even in medical conditions where the value of hemoglobin A1c is difficult to reliably assess (e.g., anemia, severe kidney disease, hemoglobinopathy) [14, 16]. GA has been used in several studies and is associated with various diseases, including atherosclerosis, peripheral artery disease, and cardiovascular and cerebrovascular diseases [10, 14, 16,17,18].

Considering its reflection period (past 2–4 weeks), GA appears to be suitable for reflecting glycemic variability prior to the onset of ischemic stroke as well as glycemic status and treatment effects during acute periods [11]. In fact, GA values are associated with various short- and long-term outcomes in patients with ischemic stroke [11, 12, 19,20,21]. A previous study examined the association between GA and early neurological deterioration (END) in patients with acute ischemic stroke (AIS) [15]. However, this study only dealt with patients with AIS and prediabetes, and there were limitations due to the small sample size and END events.

In this study, we evaluated the association between GA values and END in patients with AIS, based on data from two large medical centers in Korea. In addition, by comparing the predictive power of GA and other glycemic parameters for END, we investigated which glycemic parameter was most suitable for predicting acute outcomes in patients with stroke.

Methods

Study population

From the consecutive stroke registries of two large medical centers in Korea (Seoul Metropolitan Government-Seoul National University Boramae Medical Center and Korea University Guro Hospital), we included patients diagnosed with AIS between June 2022 and February 2023. Starting in 2022, these two centers measured GA levels in patients with AIS as part of their risk factor assessment. In addition, all AIS patients underwent a broad etiological evaluation, including brain magnetic resonance imaging, magnetic resonance angiography, echocardiography, and laboratory examinations. According to the exclusion criteria, patients who met the following criteria were excluded from the analysis: (1) arrival > 72 h after symptom onset, (2) patients without GA data. Finally, 531 patients with AIS were included in the final analysis.

Demographic, clinical, and laboratory variables

Baseline demographic and clinical variables were evaluated, including age, sex, hypertension, diabetes, dyslipidemia, atrial fibrillation, ischemic heart disease, chronic kidney disease, current smoking status, initial stroke severity, stroke mechanism, and use of thrombolytic therapy. The initial stroke severity was assessed daily from admission to discharge by a skilled neurologist not involved in the study using the National Institutes of Health Stroke Scale (NIHSS) score. The stroke mechanism was classified according to the Trial of Org 10,172 in Acute Stroke Treatment (TOAST) classification based on the evaluation results until discharge [22]. Thrombolytic therapy included intravenous thrombolysis and intra-arterial thrombectomy.

Laboratory examinations were performed within the first 24 h of admission. This included fasting glucose (mg/dL), hemoglobin A1c (%), GA (%), low-density lipoprotein (LDL) and high-density lipoprotein (HDL) cholesterol (mg/dL), triglycerides (mg/dL), white blood cell (WBC) counts (x 103/uL), and high-sensitivity C-reactive protein (hs-CRP, mg/dL). GA was obtained from the venous blood collected after a minimum of 8 h of fasting. The collected serum samples were analyzed using an enzymatic method employing albumin-specific proteinase and ketoamine oxidase. In our center, the normal range of GA values is between 11.0% and 16.0%.

Outcome variables

As the main outcome variable of this study, END was defined as an increase of two or more points in the total NIHSS score or an increase of one or more points in the motor NIHSS score within the first 72 h after admission, as in previous studies [23]. In addition, we used the modified Rankin Scale (mRS) score to measure the functional outcomes of the patients at the time of discharge. We defined an unfavorable outcome as discharge with an mRS score ≥ 3 [24].

Statistical analysis

Continuous variables with normal distributions are presented as mean ± standard deviation, whereas the others are presented as median + interquartile ranges. As GA may be an unfamiliar parameter, we analyzed the relationship between GA and various demographic, clinical, and laboratory variables to identify the characteristics of patients with high GA levels. Simple linear regression analysis was used for these analyses. Continuous variables with skewed data were adjusted by using logarithmic scales.

Subsequently, we performed a univariate analysis to identify the parameters associated with END occurrence. We used the Student’s t-test or Mann-Whitney U-test for continuous variables and the chi-squared test or Fisher’s exact test for categorical variables. Based on the results of the univariate analysis, variables with P < 0.05 and age were introduced as confounders in the multivariable logistic regression analysis. Considering the potential interaction and multicollinearity, fasting glucose and hemoglobin A1c levels were not included in the multivariable analysis, along with GA. In addition, we used GA not only as a continuous variable, but also as a categorical variable based on an appropriate cut-off value in the analysis. Based on previous studies, “GA > 16.0%” was used as the cut-off value [11, 19].

As ischemic stroke has heterogeneous mechanisms, we also compared the impact of GA on END according to the stroke mechanism. In addition, we compared the predictive power of various glycemic parameters for END occurrence. We drew receiver operating characteristic (ROC) curves and calculated the area under the curve (AUC) to quantify the predictive power. In addition, we compared the adjusted odds ratios (aORs) of each glycemic parameter based on their well-established cut-off values in the multivariable logistic regression analysis. All the statistical analyses were performed using SPSS version 23.0 (IBM Corp., Armonk, NY, USA). All variables with P < 0.05 were considered statistically significant.

Results

In total, 531 patients with AIS were evaluated (median age: 69 years, male sex: 66.3%). The median initial NIHSS score was 3 [2,3,4,5,6,7], and the median value of GA was 14.7 [13.1–17.0] %. END occurred in 96 (18.1%) patients. Other baseline characteristics are listed in Table 1.

Table 1 Baseline characteristics of the study population (n = 531)
Full size table

In our study population, GA levels were positively correlated with age, hypertension, diabetes, dyslipidemia, chronic kidney disease, hemoglobin A1c, fasting glucose levels, and hs-CRP levels. In contrast, GA levels were negatively correlated with HDL cholesterol levels (Table 2).

Table 2 Simple linear regression analysis between glycated albumin* and demographic, clinical, and laboratory risk factors
Full size table

Compared with the non-END group, the END group had a higher frequency of diabetes and thrombolytic therapy, as well as higher initial NIHSS scores, hemoglobin A1c levels, fasting glucose levels, GA levels, and WBC counts (Table 3). Multivariable logistic regression analysis demonstrated that higher GA levels were closely associated with END, even after adjusting for confounding factors (adjusted odds ratio [aOR] = 3.24, 95% confidence interval [CI]: 1.10–9.50). Initial NIHSS score (aOR = 1.04, 95% CI: 1.01–1.08) and thrombolytic therapy (aOR = 2.06, 95% CI: 1.14–3.73) were also positively associated with END, being independent from glycated albumin levels. When the multivariable analysis was performed on the basis of the cut-off point, “GA > 16.0%” also showed a close statistical association with END (aOR = 1.82, 95% CI: 1.05–3.15; Table 4).

Table 3 Baseline characteristics of groups with and without early neurological deterioration
Full size table
Table 4 Multivariable logistic regression analysis of possible predictors of early neurological deterioration
Full size table

When comparing the impact of GA on END according to the mechanism of stroke, there was a statistically significant difference in GA values between the END group and non-END group in patients with stroke caused by large artery atherosclerosis (LAA) (P = 0.014) or small vessel occlusion (SVO) (P = 0.004). In patients with stroke caused by other mechanisms, GA levels did not show a statistically significant association with END (Fig. 1).

Fig. 1
figure 1

Comparison of glycated albumin levels between END and non-END groups according to stroke mechanisms. END = early neurological deterioration, LAA = large artery atherosclerosis, SVO = small vessel occlusion, CE = cardioembolism, OD = other determined, UD = undetermined. Among various mechanisms of stroke, statistically significant differences in glycated albumin levels were observed between the END and non-END groups only in stroke patients with LAA (P = 0.014) or SVO (P = 0.004) mechanisms. In stroke patients with CE, OD, and UD, glycated albumin levels did not show a statistically significant difference in the presence of END

Full size image

In comparing the predictive power of glycemic parameters for END, GA showed a higher AUC value of 0.622 (0.560 to 0.683) on the ROC curve than fasting glucose (0.582) or hemoglobin A1c (0.578) (Figure S1). This difference in predictive power was more evident in the LAA or SVO stroke groups (Figure S2). These results were also consistent with the multivariable logistic regression analysis based on well-known cut-off values (Table S1).

Discussion

In this study, we demonstrated that higher GA values were closely associated with the occurrence of END in patients with AIS. In particular, GA appeared to be more closely involved in the occurrence of END in patients with LAA or SVO stroke. In addition, GA showed superior predictive power for END occurrence compared with other well-known glycemic parameters.

The exact mechanism underlying the close association between GA values and END is unclear. However, we propose several plausible hypotheses. First, high GA levels may indicate oxidative stress-induced endothelial dysfunction [19]. Albumin accounts for 50–60% of plasma proteins and plays a major role in human antioxidant function [10, 25]. Glycated albumin loses its antioxidant activity, which can increase reactive oxygen species and lead to the breakdown of the blood-brain barrier and damage to endothelial cells [10]. In such an environment, the initial stroke lesion is more likely to increase in size, and larger edema can occur because of impaired clearance through the glymphatic pathway [26,27,28]. In fact, recent experimental and population studies have reported that glycemic variability, rather than chronic hyperglycemia, is more likely to induce oxidative stress and is closely associated with microvascular complications [11, 15, 21]. In our data, GA values showed a close association with chronic kidney disease, another microvascular disease, while hemoglobin A1c did not show a statistically significant association, supporting this claim. Second, GA can affect atherosclerotic plaques in both cerebral large and small vessels. Similar to other glycemic parameters, GA has been shown to be closely associated with the progression or rupture of atherosclerotic plaques in several studies [10, 13, 17]. The exacerbation of atherosclerotic plaques in the cerebral vessels can contribute to the occurrence of END through in situ thrombosis, artery-to-artery embolism, and branch atheromatous disease [29]. Third, high GA levels may be associated with hemorrhagic complications following thrombolytic therapy. Previous studies have shown a strong association between high GA levels and the occurrence of hemorrhagic transformation following intravenous thrombolysis or intra-arterial thrombectomy [19, 21]. Although our study did not address hemorrhagic transformation, our data also showed a greater difference in GA values between the END and non-END groups in patients who received thrombolytic therapy than those who did not. Last, GA can reduce the effects of anti-platelet agents through platelet aggregation or activation [12, 30]. Therefore, it can lead to an increased risk of END by reducing the acute treatment effects.

There was no significant difference in the GA values according to the AIS mechanism in our study (P = 0.189). However, GA showed a better predictive value for END occurrence in patients with LAA or SVO stroke than in those with embolic stroke. Given the previously described mechanisms, such as endothelial dysfunction or plaque instability due to oxidative stress, this may be a natural result. Patients with LAA or SVO stroke can be classified into more detailed subtypes based on their underlying mechanisms (e.g., in situ thrombosis, hypoperfusion, artery-to-artery embolism, lipohyalinosis, and branch atheromatous) [29, 31]. If we conduct a subsequent study using follow-up magnetic resonance imaging in homogeneous patients with LAA or SVO stroke, we expect to identify the exact pathological mechanisms by which GA causes END in patient with AIS.

In our data, GA showed a higher predictive power for END than hemoglobin A1c or fasting glucose. To be more precise, hemoglobin A1c and fasting glucose showed AUC values that could be interpreted as virtually no correlation, and only GA showed a mild level of predictive power for END. As END is a clinical event that occurs during the acute period, it is natural that hemoglobin A1c, which reflects the average glucose concentration over the past 3 months, has poor predictive power [16, 20]. Fasting glucose can be greatly affected by factors such as diet during hospitalization, use of glucose-lowering agents, and accompanying medical conditions, and can temporarily increase by acting as an acute-phase reactant in a phenomenon called “stress hyperglycemia” after stroke occurrence [8, 9]. As various factors are complicatedly involved, fasting glucose’s predictive power for END may be unstable. However, the GA value only needs to be considered for the impact of relatively poor glycemic control. In conclusion, we believe that GA values have a higher predictive power for END than hemoglobin A1c or fasting glucose levels and that the interpretation of the results is simple. Of course, due to the characteristics of GA, it is thought that it will be difficult to monitor and correct it in real time like fasting glucose level. Rather, it would be better to classify high-risk groups for END by measuring GA levels immediately after hospitalization and establish a treatment strategy that involves intensive glucose level monitoring and management in these groups.

There are several limitations to consider when interpreting the results of this study. First, this was a retrospective cross-sectional study. Therefore, we can only present an association between GA values and END; however, this does not imply a causal relationship. By designing a prospective study that rigorously controls additional confounding variables, such as individual patient treatment strategies, comorbidities, and the timing of GA measurements, we may more clearly confirm the causal relationship between GA levels and END. Second, we analyzed the general AIS population. Therefore, to interpret our results, we must comprehensively consider the potential effect of high GA levels on various stroke mechanisms. As previously mentioned, conducting further studies on more specific stroke patient populations, including brain imaging findings (e.g., intracranial/extracranial atherosclerosis, and cerebral small vessel disease), could provide more definitive clues to the pathological mechanisms. Third, we conducted the analysis using only one GA value measured at admission. If we had measured GA values at discharge and analyzed the impact of its changes on END occurrence during the treatment period, we could have explicitly stated the impact of the actual glycemic variability and presented a basis for establishing treatment strategies. Fourth, we presented several theoretically possible mechanisms to explain the association between high GA levels and END. If specific laboratory and radiological factors that may mediate these mechanisms are included as variables or direct biochemical reactions are confirmed through laboratory studies, a clearer pathological mechanism will be defined and targeted therapy will be possible. Last, we used a relatively sensitive definition for END [32]. However, as there was a clear difference in unfavorable outcomes (mRS ≥ 3) at discharge between the non-END group and END group (Figure S3), we believe that our definition of END is clinically acceptable.

Conclusion

In conclusion, we demonstrated that high GA levels are positively associated with END in patients with AIS. GA can be easily and quickly measured using simple blood tests, and it is inexpensive. As our data demonstrated that GA had a higher predictive value for early outcomes than other glycemic parameters, we anticipate that GA could serve as a good biomarker for the initial evaluation of patients with AIS. Further prospective studies are required to validate our findings.

Data availability

No datasets were generated or analysed during the current study.

Abbreviations

GA:

Glycated albumin

END:

Early neurological deterioration

NIHSS:

National Institutes of Health Stroke Scale

TOAST:

The Trial of Org 10172 in Acute Stroke Treatment

LDL:

Low-density lipoprotein

HDL:

High-density lipoprotein

WBC:

White blood cell

hs-CRP:

High-sensitivity C-reactive protein

mRS:

Modified Rankin Scale

ROC:

Receiver operating characteristic

AUC:

Area under the curve

References

  1. Stegmayr B, Asplund K. Diabetes as a risk factor for stroke. A population perspective. Diabetologia. 1995;38:1061–8.

    Article  CAS  PubMed  Google Scholar 

  2. Bruno A, Biller J, Adams H, Clarke W, Woolson R, Williams L, Hansen M. Acute blood glucose level and outcome from ischemic stroke. Neurology. 1999;52(2):280–280.

    Article  CAS  PubMed  Google Scholar 

  3. Yong M, Kaste M. Dynamic of hyperglycemia as a predictor of stroke outcome in the ECASS-II trial. Stroke. 2008;39(10):2749–55.

    Article  PubMed  Google Scholar 

  4. Bruno A, Levine S, Frankel M, Brott T, Lin Y, Tilley B, Lyden P, Broderick J, Kwiatkowski T, Fineberg S. Admission glucose level and clinical outcomes in the NINDS rt-PA stroke trial. Neurology. 2002;59(5):669–74.

    Article  CAS  PubMed  Google Scholar 

  5. Powers WJ, Rabinstein AA, Ackerson T, Adeoye OM, Bambakidis NC, Becker K, Biller J, Brown M, Demaerschalk BM, Hoh B. Guidelines for the early management of patients with acute ischemic stroke: 2019 update to the 2018 guidelines for the early management of acute ischemic stroke: a guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2019;50(12):e344–418.

  6. Kleindorfer DO, Towfighi A, Chaturvedi S, Cockroft KM, Gutierrez J, Lombardi-Hill D, Kamel H, Kernan WN, Kittner SJ, Leira EC. 2021 guideline for the prevention of stroke in patients with stroke and transient ischemic attack: a guideline from the American Heart Association/American Stroke Association. Stroke. 2021;52(7):e364–467.

    Article  PubMed  Google Scholar 

  7. Cosentino F, Grant PJ, Aboyans V, Bailey CJ, Ceriello A, Delgado V, Federici M, Filippatos G, Grobbee DE, Hansen TB. 2019 ESC guidelines on diabetes, pre-diabetes, and cardiovascular diseases developed in collaboration with the EASD: the Task Force for diabetes, pre-diabetes, and cardiovascular diseases of the European Society of Cardiology (ESC) and the European Association for the Study of Diabetes (EASD). Eur Heart J. 2020;41(2):255–323.

    Article  PubMed  Google Scholar 

  8. Lindsberg PJ, Roine RO. Hyperglycemia in acute stroke. Stroke. 2004;35(2):363–4.

    Article  PubMed  Google Scholar 

  9. Pan Y, Cai X, Jing J, Meng X, Li H, Wang Y, Zhao X, Liu L, Wang D, Johnston SC. Stress hyperglycemia and prognosis of minor ischemic stroke and transient ischemic attack: the CHANCE study (clopidogrel in high-risk patients with acute nondisabling cerebrovascular events). Stroke. 2017;48(11):3006–11.

    Article  PubMed  Google Scholar 

  10. Song SO, Kim KJ, Lee B-W, Kang ES, Cha BS, Lee HC. Serum glycated albumin predicts the progression of carotid arterial atherosclerosis. Atherosclerosis. 2012;225(2):450–5.

    Article  CAS  PubMed  Google Scholar 

  11. Lee S-H, Jang MU, Kim Y, Park SY, Kim C, Kim YJ, Sohn J-H. Effect of prestroke glycemic variability estimated glycated albumin on stroke severity and infarct volume in diabetic patients presenting with acute ischemic stroke. Front Endocrinol. 2020;11:230.

    Article  Google Scholar 

  12. Li J, Wang Y, Wang D, Lin J, Wang A, Zhao X, Liu L, Wang C, Wang Y. Glycated albumin predicts the effect of dual and single antiplatelet therapy on recurrent stroke. Neurology. 2015;84(13):1330–6.

    Article  CAS  PubMed  Google Scholar 

  13. Moon JH, Chae MK, Kim KJ, Kim HM, Cha BS, Lee HC, Kim YJ, Lee B-W. Decreased endothelial progenitor cells and increased serum glycated albumin are independently correlated with plaque-forming carotid artery atherosclerosis in type 2 diabetes patients without documented ischemic disease. Circ J. 2012;76(9):2273–9.

    Article  CAS  PubMed  Google Scholar 

  14. Hicks CW, Wang D, Matsushita K, McEvoy JW, Christenson R, Selvin E. Glycated albumin and HbA1c as markers of lower extremity disease in US adults with and without diabetes. Diabetes Res Clin Pract. 2022;184:109212.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Lee S-H, Kim Y, Park SY, Kim C, Kim YJ, Sohn J-H. Pre-stroke glycemic variability estimated by glycated albumin is associated with early neurological deterioration and poor functional outcome in prediabetic patients with acute ischemic stroke. Cerebrovasc Dis. 2021;50(1):26–33.

    Article  CAS  PubMed  Google Scholar 

  16. Selvin E, Rawlings AM, Lutsey PL, Maruthur N, Pankow JS, Steffes M, Coresh J. Fructosamine and glycated albumin and the risk of cardiovascular outcomes and death. Circulation. 2015;132(4):269–77.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Mukai N, Ninomiya T, Hata J, Hirakawa Y, Ikeda F, Fukuhara M, Hotta T, Koga M, Nakamura U, Kang D. Association of hemoglobin A1c and glycated albumin with carotid atherosclerosis in community-dwelling Japanese subjects: the Hisayama Study. Cardiovasc Diabetol. 2015;14(1):1–11.

    Article  CAS  Google Scholar 

  18. Kim W, Kim KJ, Lee B-W, Kang ES, Cha BS, Lee HC. The glycated albumin to glycated hemoglobin ratio might not be associated with carotid atherosclerosis in patients with type 1 diabetes. Diabetes Metabolism J. 2014;38(6):456–63.

    Article  Google Scholar 

  19. Lee S-H, Jang MU, Kim Y, Park SY, Kim C, Kim YJ, Sohn J-H. High glycemic albumin representing prestroke glycemic variability is associated with hemorrhagic transformation in patients receiving intravenous thrombolysis. Sci Rep. 2022;12(1):1–8.

    Google Scholar 

  20. Kim Y, Lee S-H, Kang MK, Kim TJ, Jeong H-Y, Lee E-J, Bae J, Jeon K, Nam K-W, Yoon B-W. Glycated albumin, a Novel Biomarker for Short-Term Functional outcomes in Acute ischemic stroke. Brain Sci. 2021;11(3):337.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Lee S-H, Mo HJ, Kim Y, Park SY, Kim YJ, Lee M, Sohn J-H, Kim C. Predicting Role of Prestroke Glycemic Variability estimated by Glycated Albumin for Reperfusion and Prognosis after Endovascular Treatment. Cerebrovasc Dis. 2023;52(1):44–51.

    Article  CAS  PubMed  Google Scholar 

  22. Adams HP Jr, Bendixen BH, Kappelle LJ, Biller J, Love BB, Gordon DL, Marsh E 3rd. Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. Stroke. 1993;24(1):35–41. TOAST. Trial of Org 10172 in Acute Stroke Treatment.

  23. Nam K-W, Kang MK, Jeong H-Y, Kim TJ, Lee E-J, Bae J, Jeon K, Jung K-H, Ko S-B, Yoon B-W. Triglyceride-glucose index is associated with early neurological deterioration in single subcortical infarction: early prognosis in single subcortical infarctions. Int J Stroke. 2021;16(8):944–52.

    Article  PubMed  Google Scholar 

  24. Nam KW, Kim CK, Yu S, Oh K, Chung JW, Bang OY, Kim GM, Jung JM, Song TJ, Kim YJ. Plasma total homocysteine level is related to unfavorable outcomes in ischemic stroke with Atrial Fibrillation. J Am Heart Association. 2022;11(9):e022138.

    Article  CAS  Google Scholar 

  25. Taverna M, Marie A-L, Mira J-P, Guidet B. Specific antioxidant properties of human serum albumin. Ann Intensiv Care. 2013;3:1–7.

    Google Scholar 

  26. Cuadrado-Godia E, Dwivedi P, Sharma S, Santiago AO, Gonzalez JR, Balcells M, Laird J, Turk M, Suri HS, Nicolaides A. Cerebral small vessel disease: a review focusing on pathophysiology, biomarkers, and machine learning strategies. J Stroke. 2018;20(3):302.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Venkat P, Chopp M, Chen J. Blood–brain barrier disruption, vascular impairment, and ischemia/reperfusion damage in diabetic stroke. J Am Heart Association. 2017;6(6):e005819.

    Article  Google Scholar 

  28. Wardlaw JM, Farrall A, Armitage PA, Carpenter T, Chappell F, Doubal F, Chowdhury D, Cvoro V, Dennis MS. Changes in background blood–brain barrier integrity between lacunar and cortical ischemic stroke subtypes. Stroke. 2008;39(4):1327–32.

    Article  PubMed  Google Scholar 

  29. Bang OY. Intracranial atherosclerosis: current understanding and perspectives. J Stroke. 2014;16(1):27.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Zhao X, Li Q, Tu C, Zeng Y, Ye Y. High glycated albumin is an independent predictor of low response to clopidogrel in ACS patients: a cross-sectional study. Cardiovasc Diabetol. 2020;19:1–9.

    Article  Google Scholar 

  31. Wardlaw JM, Smith C, Dichgans M. Mechanisms of sporadic cerebral small vessel disease: insights from neuroimaging. Lancet Neurol. 2013;12(5):483–97.

    Article  PubMed  Google Scholar 

  32. Siegler JE, Martin-Schild S. Early neurological deterioration (END) after stroke: the END depends on the definition. Int J Stroke. 2011;6(3):211–2.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

None.

Funding

This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science & ICT (NRF-2020R1C1C1013304) and the Ministry of Education (NRF-2022R1I1A1A01072015). The NRF had not involve in the study design or collection, analysis, and interpretation of data.

Author information

Author notes

  1. Ki-Woong Nam and Jung Hoon Han contributed equally as first authors.

Authors and Affiliations

  1. Department of Neurology, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Korea

    Ki-Woong Nam, Hyung-Min Kwon & Yong-Seok Lee

  2. Department of Neurology, Seoul National University College of Medicine, Seoul, Korea

    Ki-Woong Nam, Hyung-Min Kwon & Yong-Seok Lee

  3. Department of Neurology, Korea University Guro Hospital, 148 Gurodong-ro, Guro-gu, Seoul, 08308, Korea

    Jung Hoon Han, Chi Kyung Kim, Kyungmi Oh & Keon-Joo Lee

  4. Department of Neurology, Korea University College of Medicine, Seoul, Korea

    Chi Kyung Kim, Kyungmi Oh & Keon-Joo Lee

  5. Department of Radiology, Korea University Guro Hospital, Seoul, Korea

    Byeongsu Park

Authors
  1. Ki-Woong Nam
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Jung Hoon Han
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Chi Kyung Kim
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Hyung-Min Kwon
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Yong-Seok Lee
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Kyungmi Oh
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Keon-Joo Lee
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Byeongsu Park
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

Conceptualization: K.-W.N. and JH.H., Data curation: Y.-S.L., K.-J.L., and BS.P., Formal analysis: K.-W.N., Funding acquisition: CK.K., Original draft preparation: K.-W.N. and JH.H, Review & editing: CK.K. and H.-M.K., Supervision: CK.K. and KM.O.

Corresponding author

Correspondence to Chi Kyung Kim.

Ethics declarations

Ethics approval and consent to participate

This retrospective cross-sectional study was approved by the Institutional Review Board (IRB) of Korea University Guro Hospital (IRB number: 2011GR0218). The IRB waived the requirement for written informed consent because of the retrospective design and use of de-identified information. All experiments were performed in accordance with the Declaration of Helsinki and the relevant guidelines and regulations.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary Material 1

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Nam, KW., Han, J.H., Kim, C.K. et al. High glycated albumin is associated with early neurological deterioration in patients with acute ischemic stroke. BMC Neurol 24, 278 (2024). https://doi.org/10.1186/s12883-024-03747-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12883-024-03747-4

Keywords

BMC Neurology

ISSN: 1471-2377

Contact us