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Oncology Letters logoLink to Oncology Letters
. 2020 May 28;20(2):1077–1082. doi: 10.3892/ol.2020.11675

Effect of dexmedetomidine on brain function and hemodynamics in patients undergoing lung cancer resection

Yunfeng Li 1, Chunyu Wang 2, Mingzhuang Bi 3, Jie Gao 4, Xue Zhang 4, Haitao Tian 5,7,
PMCID: PMC7377195  PMID: 32724346

Abstract

Effect of dexmedetomidine on the brain function and hemodynamics in patients undergoing lung cancer resection were explored. Eighty-seven patients with lung cancer undergoing lung cancer resection in Weifang People's Hospital from January 2014 to June 2018 were enrolled in this study. Patients conventionally anesthetized by propofol, midazolam, sufentanil, or cisatracurium besilate (41 cases) were assigned to the control group and those anesthetized by conventional anesthetic and dexmedetomidine (46 cases) were assigned to the research group. The hemodynamic parameters, neuron-specific enolase (NSE), and astrocyte S-100p protein (S-100β) were compared between the two groups before induction (T0), 5 min after induction (T1), at the end of surgery (T2), time of extubation (T3), and 5 min after extubation (T4). The cognitive function of patients was graded by the mini-mental state examination (MMSE) after patients recovered from anesthesia. In both the control group and the research group, the levels of mean arterial pressure (MAP), heart rate (HR), and central venous pressure (CVP). were statistically higher at T2 and T3 than those at T0 (all P<0.05). The levels of MAP, HR, and CVP were statistically lower in the research group than those in the control group at T2 and T3 (P<0.05). The levels of serum NSE and S100β protein in the research group and the control group increased at T2, T3, and T4, the control group was higher than the research group at each time point, and the difference was statistically significant (P<0.05). Comparison of the MMSE score and the total case number of adverse reactions between the two groups showed no statistical difference (both P>0.05). The MMSE score was positively correlated with the serum levels of NSE and S100β in the two groups (r-values were 0.661 and 0.585, P<0.05). Dexmedetomidine can effectively protect patients' perioperative brain function with small impacts on perioperative hemodynamics, so it is worthy of clinical application.

Keywords: dexmedetomidine, lung cancer, brain function, hemo-dynamics, cognitive function

Introduction

Lung cancer is a malignant tumor that seriously threatens human health. In recent years, China has seen a simultaneous year-on-year increase in the number of lung cancer patients and the mortality (1). Lung cancer is the leading cause of death from cancer, the principal factor for cancer death in men, and the second cancer killer of women (2).

Advancements in science and technology have significantly improved the early diagnosis rate of lung cancer. Surgery is the preferred treatment for most patients, but the anesthesia and surgical trauma often cause a stress response. Trauma or surgical injury can activate immune inflammation and neuroendocrine reactions, leading to ischemic brain damage (3). The subsequent destruction of the blood-brain barrier causes brain dysfunction, leading to postoperative cognitive dysfunction (POCD) (4). As the main complication that contributes to disability and distress in millions of patients every year (5), POCD results in prolonged hospital stay, weakened physical functions, and increased mortality (6,7), which severely damages the prognosis and quality of life of patients. So the rational use of anesthetic drugs is crucial for the treatment and prognosis of patients.

Dexmedetomidine is an α-2 adrenergic receptor agonist with sedative and analgesic effects, widely used for general anesthesia (8). Extubation during surgery can induce hemodynamic changes. Studies have reported that (9,10) dexmedetomidine has a biphasic hemodynamic effect. It can regulate the release of norepinephrine and inhibit sympathetic activity, thereby reducing the release of inflammatory factors and stabilizing blood pressure. Dexmedetomidine can reduce the risk of hypertension and tachycardia in neurosurgical patients (11,12) and is widely used clinically.

So far, there have been few reports on the effects of dexmedetomidine on brain function and hemodynamics in patients with lung cancer resection. Therefore, this study assessed the cognitive function and hemodynamic parameters in patients receiving dexmedetomidine anesthesia.

Patients and methods

Basic patient information

Eighty-seven patients with lung cancer undergoing lung cancer resection in Weifang People's Hospital (Weifang, China) from January 2014 to June 2018 were enrolled in this study. There were 41 patients undergoing conventional anesthesia in the control group and 46 patients undergoing conventional anesthesia and dexmedetomidine anesthesia in the research group. The two groups were not notably different regarding age, sex, and other basic information.

Inclusion criteria: Patients diagnosed with lung cancer and willing to receive surgical resection; patients not treated with radiotherapy or chemotherapy before; patients with no other malignant tumors. Exclusion criteria: Patients with liver and kidney dysfunction or communicative and cognitive impairment; patients who did not cooperate with the experiment. All patients and their families agreed to participate in the experiment and signed an informed consent form. This study was approved by the Ethics Committee of the hospital.

Methods

The venous access was established at the beginning of the operation and the basic vital signs of patients were under close monitoring. In this study, propofol, midazolam, sufentanil, and cisatracurium besilate were used for conventional anesthesia. Patients in the control group underwent conventional anesthesia, while patients in the research group underwent conventional anesthesia and dexmedetomidine anesthesia (Sinopharm Group Guorui Medicine Co., Ltd.) through intravenous injection at an initial dose of 0.5 µg/kg and then at a fixed dose of 0.1 µg/kg-1 h-1. Elbow venous blood (5 ml) was drawn from all patients at T0, T1, T2, T3, and T4, respectively, and then centrifuged at 1,500 × g and 4°C for 10 min. Then the supernatant was collected and placed at −80°C in a refrigerator for later use. The expression levels of neuron-specific enolase (NSE) and S-100β in the serum of the patients were determined by enzyme-linked immunosorbent assay (ELISA) in strict accordance with the kit manuals. All kits were from Shanghai Guangrui Biological Co., Ltd.

Outcome measures. a) Hemodynamic parameters at different time points in the two groups: mean arterial pressure (MAP), heart rate (HR), and central venous pressure (CVP). b) Expression levels of NSE and S-100β at different time points in the two groups. c) Cognitive function indicated by the mini-mental state examination (MMSE) score in the two groups before the anesthesia and after the recovery from anesthesia. d) The case number of adverse reactions in the two groups. e) Correlation analysis between MMSE scores and serum NSE and S100β levels in the two groups.

Statistical analysis. Statistical analysis was performed on SPSS 20.0 software. The measurement data were expressed as the mean ± standard deviation (mean ± SD). t-test was used for intergroup comparison and paired t-test was used for intra-group comparison. The count data were expressed by n/% and intergroup comparison was performed by the χ2 test. Correlation analysis was performed using the Spearman correlation coefficient. The difference was considered statistically significant at P<0.05.

Results

Comparison of the basic information between the two group

The two groups were not statistically different in age, BMI, and other basic information (P>0.05) (Table I).

Table I.

Comparison of basic information.

Factors Research group (n=41) Control group (n=46) t/χ2 P-value
Age (year) 67.37±3.27 67.26±2.07 0.190 0.850
BI (kg/m2)   21.3±2.45   21.5±2.36 0.388 0.699
Sex
  Male 21 (51.22) 24 (52.17)
  Female 20 (48.78) 22 (47.83) 0.008 0.939
Hypertension
  Yes 18 (43.90) 20 (43.48)
  No 23 (56.10) 26 (56.52) 0.002 0.968
Diabetes
  Yes 19 (46.34) 21 (45.65)
  No 22 (53.66) 25 (54.35) 0.004 0.949
Hyperlipemia
  Yes 20 (48.78) 24 (52.17)
  No 21 (51.22) 22 (47.83) 0.099 0.752
Smoking
  Yes 28 (68.29) 27 (58.70)
  No 13 (31.71) 19 (41.30) 0.859 0.354
Drinking
  Yes 25 (60.98) 26 (56.52)
  No 16 (39.02) 20 (43.48) 0.177 0.673

Hemodynamic parameters at different time points in the two groups

In both the control group and the research group, the levels of MAP, HR, and CVP were statistically higher at T2 and T3 than those at T0 (all P<0.05). The levels of MAP, HR, and CVP were statistically lower in the research group than those in the control group at T2 and T3 (P<0.05) (Table II).

Table II.

Hemodynamic parameters at different time points in the two groups.

Group Time MAP /kPa HR (beat/min) CVP (mmHg)
Research group (n=41) T0 10.2±1.6 82.61±7.34 88.61±5.25
T1 10.4±1.4 81.60±7.35 87.61±5.35
T2 11.0±1.5a,b,e 85.37±8.35a,b,e 91.61±6.25a,b,e
T3 11.4±1.4a,b,e 88.61±8.25a,b,e 93.61±6.35a,b,e
T4 10.3±1.3c,d 83.60±7.34c,d 86.61±5.45c,d
Control group (n=46) T0 10.4±1.2 81.95±8.43 87.61±5.23
T1 10.5±1.3 80.95±8.43 88.61±5.35
T2 11.8±1.6a,b 95.38±7.68a,b 95.61±6.53a,b
T3 12.4±1.5a,b 97.38±7.58a,b 97.61±6.46a,b
T4 10.3±1.6c,d 82.38±8.32c,d 86.61±5.34c,d
a

P<0.05 when compared with T0 within the group

b

P<0.05 when compared with T1 within the group

c

P<0.05 when compared with T2 within the group

d

P<0.05 when compared with T3 within the group

e

P<0.05 when compared with T4 within the group. MAP, mean arterial pressure; HR, heart rate; CVP, central venous pressure.

The expression levels of serum NSE and S100β at different time points in the two groups

The levels of serum NSE and S100β protein in the research group and the control group increased at T2, T3, and T4, higher in control group than those in the research group at each time point, and the difference was statistically significant (P<0.05) (Table III).

Table III.

Expression levels of serum NSE and S100β at different time points in the two groups.

Group Time NSE (µg/l) S100β (µg/l)
Research group (n=41) T0 0.14±0.03 5.67±1.56
T1 0.15±0.04 5.72±1.62
T2 0.76±0.13a,b,e 6.62±1.78a,b,e
T3 0.82±0.18a,b,e 6.89±1.93a,b,e
T4 0.98±0.21ae 7.79±1.98ae
Control group (n=46) T0 0.13±0.03 5.68±1.46
T1 0.15±0.05 5.82±1.36
T2 1.26±0.13a,b 8.67±1.16a,b
T3 1.30±0.12a,b 8.87±1.26a,b
T4 1.43±0.15ad 9.37±1.36ad
a

P<0.05 when compared with T0 within the group

b

P<0.05 when compared with T1 within the group

c

P<0.05 when compared with T2 within the group

d

P<0.05 when compared with T3 within the group

e

P<0.05 when compared with T4 within the group. NSE, neuron-specific enolase.

MMSE scores in the two groups before the anesthesia and after the recovery from anesthesia

The comparison of MMSE scores before anesthesia and after recovery from anesthesia showed no statistical difference between the two groups (P>0.05) (Table IV).

Table IV.

MMSE scores in the two groups before the anesthesia and after the recovery from anesthesia.

Group Research group (n=41) Control group (n=46) t P-value
Before the anesthesia 28.54±4.34 28.48±4.25 0.065 0.948
After the recovery from anesthesia 27.34±2.45 27.21±3.11 0.215 0.831

MMSE, mini-mental state examination.

Case number of adverse reactions in the two groups

One case of hypotension and 1 case of sinus bradycardia were reported in the research group, while 1 case of hypotension, 2 cases of sinus bradycardia, and 2 cases of sinus tachycardia were reported in the control group. The two groups were not statistically different in the total number of adverse reactions (P>0.05) (Table V).

Table V.

Case number of adverse reactions in the two groups.

Group Research group (n=41) Control group (n=46) χ2 P-value
Hypotension 1 (2.44) 1 (2.17) 0.007 0.934
Sinus bradycardia 1 (2.44) 2 (4.35) 0.237 0.626
Sinus tachycardia 0 2 (4.35) 1.825 0.177
Total number of adverse reactions 2 (4.88) 5 (10.87) 1.052 0.305

Correlation analysis between MMSE scores and serum NSE and S100β levels

The MMSE scores of the two groups were positively correlated with the expression levels of serum NSE and S100β (P<0.001) (Fig. 1).

Figure 1.

Figure 1.

Correlation analysis between MMSE scores and serum NSE and S100β levels. (A) MMSE scores were positively correlated with NSE levels in the two groups (r=0.661, P<0.001). (B) MMSE scores were positively correlated with S-100β levels in the two groups (r=0.585, P<0.001). MMSE, mini-mental state examination; NSE, neuron-specific enolase.

Discussion

Good anesthesia can increase the success rate of surgery, reduce intraoperative inflammation and stress response, and improve the prognosis and recovery of postoperative organ function (13). Dexmedetomidine can inhibit neuronal discharge to achieve resistance to anxiety, suppress sympathetic nerve activity, reduce neuronal apoptosis, and alleviate the body's inflammatory response (3). Lung cancer resection, a common surgery for lung cancer treatment, leads to high risk of POCD in patients, which manifests as insanity, anxiety, and personality changes. These complications may be associated with factors such as anesthesia methods, types of surgery, and cognitive differences (14). Elderly patients general have other organ diseases such as cardiovascular disease, which will increase the risk of intubation. Therefore, monitoring the patient's hemodynamics and maintaining its stability is also important during the surgical anesthesia. This study aimed to explore the effect of dexmedetomidine on the brain function and hemodynamics in patients undergoing lung cancer resection.

In our study, MAP, HR, and CVP levels were significantly increased at T2 and T3 in both the control group and the research group, with higher levels in the research group, suggesting that the control group underwent great hemodynamic fluctuations, while dexmedetomidine effectively maintained the hemodynamic stability in the research group. The reason why dexmedetomidine contributes to hemodynamic stability may be that dexmedetomidine is involved in the systemic circulation so as to achieve sedation and analgesia and suppress the sympathetic nervous system activity. A previous study (15) reported that dexmedetomidine stabilized the hemodynamics of patients undergoing head and neck reconstruction. Another study (16) stated that intraoperative dexmedetomidine could better control postoperative MAP and provide a better analgesic effect for patients with craniotomy, which is consistent with the results of this study.

NSE is a highly specific marker for neuronal and peripheral neuroendocrine cells. When NSE is found in specific tissues under normal conditions, its increased body fluid levels may be accompanied by malignant proliferation and thus be valuable in the diagnosis, staging, and treatment of neuroendocrine tumors (17,18). S100B is a calcium-binding protein found mainly in mature perivascular astrocyte cytoplasms (19). S100B protein and NSE are the most studied serum markers in the field of brain injury (20). In this study, serum expression levels of NSE and S100β were increased at T2, T3, and T4 in the research group and the control group. Serum expression levels of NSE and S100β protein were higher in the control group than those in the research group at each time point, and the MMSE scores of the two groups were positively correlated with the expression levels of NSE and S100β, suggesting that the severity of cognitive impairment was positively correlated with the expression levels of NSE and S100β. So we speculate that the expression levels of NSE and S100β can be used to monitor the postoperative cognitive impairment in patients. The study by Zhang et al (21) found that the increase in serum NSE and S100-β levels was correlated with the occurrence of cognitive impairment in patients with brain injury. Chaves et al (22) considered that higher S100β protein levels led to worse cognitive function, higher NSE level, and more severe brain atrophy. Therefore, the use of dexmedetomidine before anesthesia induction can reduce serum NSE and S100-β protein levels and improve the stability of cognitive functions in patients. No marked difference was shown in the total case number of adverse reactions and MMSE scores between the two groups before the anesthesia and after the recovery from anesthesia, indicating that dexmedetomidine is safe and worthy of clinical application and promotion.

In conclusion, the use of dexmedetomidine before the anesthesia induction can stabilize the hemodynamic parameters and certainly protect the brain function. However, the results of this study need to be further verified due to the small sample size.

Acknowledgements

Not applicable.

Funding

Key Research and Development Projects in Shandong (2018GSF118216); Development Plan of Medical and Health Science and Technology Projects in Shandong province (2017WS524).

Availability of data and materials

The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.

Authors' contributions

YL, CW, MB and HT led the conception and design of this study. YL, CW, JG, XZ and HT were responsible for the data collection and analysis. YL, MB and JG were in charge of interpreting the data and drafting the manuscript. CW and HT made revision from critical perspective for important intellectual content. The final version was read and adopted by all the authors.

Ethics approval and consent to participate

The study was approved by the Ethics Committee of Weifang People's Hospital (Weifang, China). Signed informed consents were obtained from the patients and/or the guardians.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.


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