Intestinal barrier dysfunction is involved in the development of systemic inflammatory responses and lung injury in type A aortic dissection: a case-control study.

Background: The definite pathogenesis of lung injury complicated by type A aortic dissection (TAAD) remains unclear. In this paper, we investigated the relationship between intestinal injury, lung injury, and systemic inflammatory responses, with the aim of exploring the mechanism underlying intestinal injury and its impact on systemic inflammatory responses and lung injury in patients with TAAD.
Methods: Patients with TAAD (n=36) and those with aortic root aneurysm (ARA) (n=30) were compared. TAAD patients were younger and had higher creatinine (Cr) than ARA patients. White blood cell (WBC) count, neutrophil count, neutrophil percentage, interleukin (IL)-6, IL-8, tumor necrosis factor α (TNF-α), C-reactive protein (CRP), histamine (HIS) levels, PaO2-FiO2 ratio, diamine oxidase (DAO), intestinal fatty acid binding protein (iFABP), and peptidoglycan (PGN) were measured using the same laboratory methods between the two groups.
Results: Increased WBC [(9.70±4.05)×109/L vs. (5.88±1.2)×109/L, P<0.001], neutrophil [(7.65±4.27)×109/L vs. (3.40±0.97)×109/L, P<0.001], neutrophil percentage [(74.73±13.42)% vs. (57.67±9.45)%, P<0.001], IL-6 (37.48±4.87 vs. 20.90±0.92 pg/mL, P<0.001), IL-8 (97.15±9.11 vs. 69.46±3.17 pg/mL, P<0.001), TNF-α (71.32±10.35 vs. 33.90±2.27 pg/mL, P<0.001), CRP (10.67±1.62 vs. 4.43±0.26 µg/mL, P<0.001), HIS (13.29±1.88 vs. 7.63±0.58 ng/mL, P<0.001), DAO (24.94±4.72 vs. 10.92±2.44 U/L, P<0.001), iFABP (879.01±190.12 vs. 206.35±42.20 pg/mL, P<0.001), and PGN (31.10±5.51 vs. 12.52±2.20 ng/mL, P<0.001) and decreased PaO2-FiO2 ratio (365.35±146.47 vs. 447.86±70.80 mmHg, P=0.01) were detected in TAAD group relative to ARA group. In TAAD group, positive correlations were detected between DAO and inflammatory cytokines [IL-6 (r=0.56, P<0.001), IL-8 (r=0.61, P<0.001), TNF-α (r=0.71, P<0.001), and CRP (r=0.68, P<0.001)], between iFABP and inflammatory cytokines [IL-6 (r=0.72, P<0.001), IL-8 (r=0.71, P<0.001), TNF-α (r=0.90, P<0.001), and CRP (r=0.89, P<0.001)], between DAO and PGN (r=0.52, P<0.001), between iFABP and PGN (r=0.74, P<0.001), between PGN and inflammatory cytokines [IL-6 (r=0.85, P<0.001), IL-8 (r=0.44, P<0.001), TNF-α (r=0.61, P<0.001), and CRP (r=0.73, P<0.001)]. In acute TAAD subgroup, PGN and PaO2-FiO2 ratio were negatively correlated (r=-0.50, P=0.036). Conclusions: Systemic inflammatory responses in TAAD patients may lead to lung and intestine injury, and the latter may be involved in the development of systemic inflammatory responses and lung injury in these patients. 2022 Journal of Thoracic Disease. All rights reserved.

Introduction

The annual incidence of aortic dissection is approximately 3.5/100,000 (1), equating to an estimated 50,000 new cases every year in China. Type A aortic dissection (TAAD) is the most common aortic catastrophe, with an extremely high lethality rate of 1–2% per hour after symptom onset and 74% within 2 weeks in untreated patients (2). Acute lung injury is a serious complication of acute TAAD, which occurs in approximately 50% of patients and can be life-threatening in severe cases (3-5). Some studies have revealed the significant involvement of systemic inflammatory responses in the development of acute lung injury in patients with acute TAAD (3-11). It was generally believed that long-term chronic inflammation in the aortic wall, contributing greatly to aortic wall remodeling (similar to the main histological finding described in aortic aneurysm), rapidly progresses to acute systemic inflammatory responses when acute aortic dissection occurs (5,12-15). Recently, a study found that intestinal barrier dysfunction can occur in patients with acute TAAD and may be important for the development of systemic inflammatory responses and acute lung injury (16). However, gaps remain in our knowledge as to whether the levels of systemic inflammatory responses and intestinal barrier dysfunction are different between patients with acute TAAD and non-acute aortic diseases, such as aortic aneurysm and non-acute TAAD, in which acute lung injury rarely occurs. In this study, we investigated intestinal injury, lung injury, and systemic inflammatory responses in patients with acute TAAD, non-acute TAAD, and aortic root aneurysm (ARA), and their relationships with each other, in order to explore the mechanism underlying intestinal injury, lung injury, and systemic inflammatory responses in patients with TAAD. We believe that this study may be helpful for the development of future therapeutic strategies for acute lung injury in patients with acute TAAD, regarding to the protection for intestinal barrier function. We present the following article in accordance with the STROBE reporting checklist (available at https://jtd.amegroups.com/article/view/10.21037/jtd-22-1122/rc).

Methods

Study population and sample collection

This was a single-center, observational case-control study. From January 2016 to April 2016, 42 patients with TAAD and 36 patients with ARA were admitted to our institution. TAAD and ARA were diagnosed based on clinical symptoms, echocardiography, and aortic computed tomography angiography. TAAD was defined as an intimal tear and double lumen separated by the septum involving the ascending aorta, and ARA was defined as an aortic root of greater than 4.5 cm in diameter (1). The acute phase of dissection was defined as the time from symptom onset to admission within 14 days. The exclusion criteria included renal insufficiency, autoimmune diseases, lung diseases, gastrointestinal diseases, liver diseases, or malperfusion of the heart, brain, gastrointestinal tract, liver, pancreas, kidney, or limbs. Of the patients admitted, 5 patients refused to participate in the study, and 7 patients met at least 1 of the exclusion criteria. The remaining 36 patients with TAAD and 30 patients with ARA were enrolled in this study. Of the 36 patients with TAAD, 18 had acute TAAD (≤14 days), while the remaining 18 patients had non-acute (>14 days) TAAD. Blood samples were collected on admission, from which serum samples were obtained after centrifugation and stored at −80 ℃. Serum samples pertaining to TAAD and ARA were always analyzed together in the same batch and laboratory personnel were unable to distinguish among TAAD and ARA samples. In order to reduce selection bias, all cases of TAAD and ARA were reviewed by 2 experienced cardiologists, using diagnostic criteria and exclusion criteria, to ensure appropriate inclusion of cases. Disagreements were noted and discussed between reviewers. The minimum sample size that we needed was 9 cases for each group, with 80% power and 5% significance. The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). This study was approved by the Ethics Committee of Beijing Anzhen Hospital, Capital Medical University (No. GZR 046), and written informed consent was obtained from all patients and/or immediate relatives.

Data collection and measurements

Baseline study population characteristics

Patient data were obtained by reviewing medical records, including age, sex, history of smoking, hypertension, diabetes, coronary heart disease, and cerebral infarction. Admission biochemical measurements were also obtained, including creatinine (Cr), alanine aminotransferase (ALT), aspartate aminotransferase (AST), D-dimer, and lactic acid levels.

Systemic inflammatory response levels

Admission white blood cell (WBC) parameters, including WBC count, neutrophil count, and neutrophil percentage, were obtained by reviewing medical records. Admission inflammatory cytokines [interleukin (IL)-6, IL-8, tumor necrosis factor α (TNF-α), C-reactive protein (CRP), and histamine (HIS)] were measured in serum collected as described above using the enzyme-linked immunosorbent assay technique (R&D Systems, Minneapolis, MN, USA), according to the manufacturer’s instructions.

Lung injury, intestinal injury, and bacteremia levels

Lung injury extent was determined by reviewing the admission PaO2-FiO2 ratio in the medical records. The level of intestinal injury was assessed by measuring diamine oxidase (DAO) activity and the concentration of intestinal fatty acid binding protein (iFABP), and bacteremia level was determined by measuring peptidoglycan (PGN) concentration in serum collected as described above. DAO activity was determined by spectrophotography (Sigma-Aldrich, Louis, MO, USA), and iFABP and PGN were measured using enzyme-linked immunosorbent assays (R&D Systems), according to the manufacturer’s instructions.

Statistical analysis

Continuous variables are expressed as mean ± standard deviation, and the tests of normality of continuous outcomes were performed. Independent sample t-tests or t'-tests were used for comparisons between the TAAD group and ARA group and between the acute TAAD subgroup and non-acute TAAD subgroup. Analyses of covariance were used to adjust for potential confounders in baseline characteristics, if necessary. Qualitative variables are expressed as rates, and chi-square tests, corrected chi-square tests, or Fisher’s exact probability tests were used for comparisons between 2 groups. Correlations were assessed by calculating Pearson correlation coefficient values. Sample size calculations were performed based on coefficient of variation with 80% power and 5% significance. There were some missing values in the variables of D-dimer, lactic acid, and PaO2-FiO2 ratio and no missing values in the other variables in this study, which may not affect the main outcomes of this study regarding systemic inflammatory responses, intestinal injury, bacteremia, and their relationships. These missing values, including 2 for D-dimer in ARA, 6 for lactic acid in TAAD, 9 for lactic acid in ARA, 5 for PaO2-FiO2 ratio in TAAD, and 9 for PaO2-FiO2 ratio in ARA not to be tested owing to the physician’s prescribing preference and recorded in medical records, can be regarded as ignorable according to the assumption of missing at random. Two-sided P<0.05 was considered to indicate a statistically significant difference. Statistical analyses were performed using SPSS 22.0 for Windows (IBM SPSS, Armonk, NY, USA).

Results

Study population demographic characteristics

A total of 66 individuals were included in the study, and their baseline characteristics are summarized in . Patients in the TAAD group were younger and had higher serum Cr levels on admission than those in the ARA group and no significant differences were observed in sex, medical history, or other clinical variables between the two groups. Patients in the acute TAAD subgroup had higher serum Cr levels than those in the non-acute subgroup and no significant differences were observed in age, sex, medical history, or other clinical variables between the two subgroups (). Analyses of covariance were used for comparisons in the levels of systemic inflammatory response and the levels of lung injury, intestinal injury, and bacteremia between the TAAD group and ARA group and between the acute TAAD subgroup and non-acute TAAD subgroup to adjust for potential confounders in baseline characteristics, including age and serum Cr levels.

Table 1

Baseline characteristics of TAAD and ARA groups

Clinical variable	TAAD	ARA	P
Number, n	36	30
Age, years, mean ± SD	45.25±11.65	51.57±12.76	0.040
Men, n (%)	31 (86.1)	25 (83.3)	0.754
Smoker, n (%)	16 (44.4)	13 (43.3)	0.928
Hypertension, n (%)	21 (58.3)	13 (43.3)	0.225
Diabetes, n (%)	0	1 (3.3)	0.455
Coronary heart disease, n (%)	0	2 (6.7)	0.203
Cerebral infarction, n (%)	0	2 (6.7)	0.203
Serum measurements, mean ± SD
Cr, μmol/L	103.21±52.26	80.03±16.75	0.016
ALT, U/L	38.39±44.03	24.57±13.85	0.082
AST, U/L	34.61±32.35	24.03±9.38	0.069
D-dimer, mmol/L	3,550.67±11,518.63	404.36±1,274.59	0.156
Lactic acid, ng/mL	1.72±1.12	1.85±0.56	0.630

TAAD, type A aortic dissection; ARA, aortic root aneurysm; SD, standard deviation; Cr, creatinine; ALT, alanine aminotransferase; AST, aspartate aminotransferase.

Table 2

Baseline characteristics of acute and non-acute TAAD subgroups

Clinical variable	Acute TAAD	Non-acute TAAD	P
Number, n	18	18
Age, years, mean ± SD	47.00±11.11	43.50±12.21	0.375
Men, n (%)	17 (94.4)	14 (77.8)	0.338
Smoker, n (%)	8 (50.0)	8 (50.0)	1.000
Hypertension, n (%)	11 (61.1)	10 (55.6)	1.000
Diabetes, n (%)	0	0	–
Coronary heart disease, n (%)	0	0	–
Cerebral infarction, n (%)	0	0	–
Serum measurements, mean ± SD
Cr, μmol/L	122.62±66.43	83.80±20.30	0.028
ALT, U/L	31.17±25.39	45.61±56.89	0.332
AST, U/L	31.00±19.86	38.22±41.63	0.511
D-dimer, mmol/L	6,469.11±15,954.76	632.22±755.85	0.139
Lactic acid, ng/mL	1.99±1.36	1.37±0.57	0.102

TAAD, type A aortic dissection; SD, standard deviation; Cr, creatinine; ALT, alanine aminotransferase; AST, aspartate aminotransferase.

Systemic inflammatory response levels

In patients with TAAD, WBC count [(9.70±4.05)×109/L vs. (5.88±1.2)×109/L, P<0.001, ], neutrophil count [(7.65±4.27)×109/L vs. (3.40±0.97)×109/L, P<0.001, ], and neutrophil percentage [(74.73±13.42)% vs. (57.67±9.45)%, P<0.001, ] were significantly elevated compared to those in the ARA group. Serum levels of IL-6 (37.48±4.87 vs. 20.90±0.92 pg/mL, P<0.001, ), IL-8 (97.15±9.11 vs. 69.46±3.17 pg/mL, P<0.001, ), TNF-α (71.32±10.35 vs. 33.90±2.27 pg/mL, P<0.001, ), CRP (10.67±1.62 vs. 4.43±0.26 µg/mL, P<0.001, ), and HIS (13.29±1.88 vs. 7.63±0.58 ng/mL, P<0.001, ) were significantly higher in patients with TAAD than in those with ARA.

Figure 1

Comparison of systemic inflammatory response levels between TAAD and ARA. (A) WBC count; (B) Neutrophil count; (C) Neutrophil percentage; (D) IL-6; (E) IL-8; (F) TNF-α; (G) CRP, (H) HIS. (A-H) Two-tailed analysis of covariance, ***, P<0.001. TAAD, n=36; ARA, n=30. Star (★) indicates extremes, which are values more than 3 interquartile ranges from the end of a box. Circle (○) indicates outliers, which are values between 1.5 interquartile ranges and 3 interquartile ranges from the end of a box. WBC, white blood cell; TAAD, type A aortic dissection; ARA, aortic root aneurysm; IL, interleukin; TNF-α, tumor necrosis factor α; CRP, C-reactive protein; HIS, histamine.

In patients with acute TAAD, WBC count [(12.35±3.83)×109/L vs. (7.05±2.08)×109/L, P<0.001, ], neutrophil count [(10.48±4.03)×109/L vs. (4.82±2.07)×109/L, P<0.001, ], and neutrophil percentage [(82.88±9.13)% vs. (66.58±12.12)%, P<0.001, ] were significantly elevated compared to those in patients with non-acute TAAD. No significant differences in IL-6 (38.29±2.90 vs. 36.67±6.25 pg/mL, P=0.330), IL-8 (98.27±4.94 vs. 96.02±12.00 pg/mL, P=0.468), TNF-α (73.72±3.86 vs. 68.92±13.91 pg/mL, P=0.168), CRP (11.13±0.42 vs. 10.22±2.19 µg/mL, P=0.099), or HIS (13.53±1.41 vs. 13.04±2.28 ng/mL, P=0.448) were observed between the acute and non-acute TAAD groups.

Figure 2

Comparison of systemic inflammatory response levels between acute and non-acute TAAD. (A) WBC count; (B) neutrophil count; (C) neutrophil percentage. (A-C) Two-tailed analysis of covariance, ***, P<0.001. Acute TAAD, n=18; non-acute TAAD, n=18. Circle (○) indicates outliers, which are values between 1.5 interquartile ranges and 3 interquartile ranges from the end of a box. WBC, white blood cell; TAAD, type A aortic dissection.

Levels of lung injury, intestinal injury, and bacteremia

The PaO2-FiO2 ratio was significantly lower in patients with TAAD than in those with ARA (365.35±146.47 vs. 447.86±70.80 mmHg, P=0.01, ). Moreover, the PaO2-FiO2 ratio was significantly lower (273.39±98.04 vs. 492.69±98.80 mmHg, P<0.001, ) in patients with acute TAAD compared to those with non-acute TAAD.

Figure 3

Levels of lung injury, intestinal injury, and bacteremia. (A) Comparison of PaO2-FiO2 ratio between TAAD and ARA, two-tailed analysis of covariance, **, P=0.01. (B) Comparison of PaO2-FiO2 ratio between acute and non-acute TAAD; (C) comparison of DAO activity between TAAD and ARA; (D) comparison of iFABP between TAAD and ARA; (E) comparison of PGN between TAAD and ARA. (B-E) Two-tailed analysis of covariance, ***, P<0.001. TAAD, n=36; ARA, n=30. Acute TAAD, n=18; non-acute TAAD, n=18. Star (★) indicates extremes, which are values more than 3 interquartile ranges from the end of a box. Circle (○) indicates outliers, which are values between 1.5 interquartile ranges and 3 interquartile ranges from the end of a box. TAAD, type A aortic dissection; ARA, aortic root aneurysm; DAO, diamine oxidase; iFABP, intestinal fatty acid binding protein; PGN, peptidoglycan.

DAO activity (24.94±4.72 vs. 10.92±2.44 U/L, P<0.001, ), iFABP (879.01±190.12 vs. 206.35±42.20 pg/mL, P<0.001, ), and PGN (31.10±5.51 vs. 12.52±2.20 ng/mL, P<0.001, ) were significantly elevated in patients with TAAD compared to those with ARA. No significant differences in DAO activity (25.61±3.29 vs. 24.27±5.83 U/L, P=0.402), iFABP (930.71±64.39 vs. 827.31±254.19 pg/mL, P=0.111), or PGN (32.27±3.63 vs. 29.92±6.80 ng/mL, P=0.205) were observed between patients with acute and non-acute TAAD.

Correlations among systemic inflammatory responses, lung injury, intestinal injury, and bacteremia

In patients with TAAD, significant positive correlations were detected between DAO activity and inflammatory cytokine levels, including IL-6 (r=0.56, P<0.001, ), IL-8 (r=0.61, P<0.001, ), TNF-α (r=0.71, P<0.001, ), and CRP (r=0.68, P<0.001, ). Furthermore, significant correlations were detected between iFABP and inflammatory cytokine levels, including IL-6 (r=0.72, P<0.001, ), IL-8 (r=0.71, P<0.001, ), TNF-α (r=0.90, P<0.001, ), and CRP (r=0.89, P<0.001, ).

Figure 4

Correlations between systemic inflammatory responses and intestinal injury indicators in TAAD. (A) Relationship between IL-6 and DAO; (B) relationship between IL-8 and DAO; (C) relationship between TNF-α and DAO; (D) relationship between CRP and DAO; (E) relationship between IL-6 and iFABP; (F) relationship between IL-8 and iFABP; (G) relationship between TNF-α and iFABP; (H) relationship between CRP and iFABP. Pearson correlation. TAAD, n=36. IL, interleukin; TNF-α, tumor necrosis factor α; CRP, C-reactive protein; HIS, histamine; DAO, diamine oxidase; iFABP, intestinal fatty acid binding protein; TAAD, type A aortic dissection.

In patients with TAAD, significant positive correlations were also found between DAO activity and PGN (r=0.52, P<0.001, ) as well as between iFABP and PGN (r=0.74, P<0.001, ).

Figure 5

Correlation between intestinal injury and bacteremia in TAAD. (A) Relationship between PGN and DAO; (B) relationship between PGN and iFABP. Pearson correlation. TAAD, n=36. PGN, peptidoglycan; DAO, diamine oxidase; iFABP, intestinal fatty acid binding protein; TAAD, type A aortic dissection.

Significant positive correlations were found between PGN and several inflammatory cytokines, including IL-6 (r=0.85, P<0.001, ), IL-8 (r=0.44, P<0.001, ), TNF-α (r=0.61, P<0.001, ), and CRP (r=0.73, P<0.001, ), in patients with TAAD.

Figure 6

Correlation between bacteremia and systemic inflammatory responses in TAAD. (A) Relationship between IL-6 and PGN; (B) relationship between IL-8 and PGN; (C) relationship between TNF-α and PGN; (D) relationship between CRP and PGN. Pearson correlation. TAAD, n=36. IL, interleukin; TNF-α, tumor necrosis factor α; CRP, C-reactive protein; PGN, peptidoglycan; TAAD, type A aortic dissection.

In addition, in patients with acute TAAD, serum PGN level and PaO2-FiO2 ratio value were significantly negatively correlated (r=−0.50, P=0.036, ).

Figure 7

Correlation between bacteremia and lung injury in acute TAAD. Relationship between PaO2-FiO2 ratio and PGN. Pearson correlation. Acute TAAD, n=18. PGN, peptidoglycan; TAAD, type A aortic dissection.

Discussion

Acute lung injury, defined as PaO2-FiO2 ratio <300 mmHg, occurs in approximately 50% of patients with acute TAAD and can be life-threatening in severe cases (3-5). Preoperative hypoxemia can result in surgery delay, which increases the risk of aortic rupture, cardiac tamponade, or even death (17). Patients with acute TAAD and preoperative acute lung injury are at increased risk of postoperative acute respiratory distress syndrome and have prolonged intubation times and/or increased mortality rates after surgery (18). Preoperative acute lung injury can also result in more intraoperative blood loss, longer mechanical ventilation time, and a longer stay in the intensive care unit and hospital (4). Preoperative acute lung injury develops mainly in patients with acute TAAD, but rarely occurs in non-acute aortic diseases, such as aortic aneurysm and non-acute TAAD. In this study, we found that the PaO2-FiO2 ratio was significantly lower in patients with acute TAAD than in those with non-acute TAAD or ARA, and the incidence of PaO2-FiO2 ratio <300 mmHg was 66.67% (12/18) in patients with acute TAAD and 0 in non-acute TAAD or ARA. These findings indicated that significant lung injury developed during the acute period of TAAD and was alleviated after the acute phase, with lung function tending to normalize.

The definite pathogenesis of acute lung injury complicated by acute TAAD remains unclear. It is currently considered that systemic inflammatory reactions play important roles in the development of acute lung injury. IL-6, TNF-α, and CRP are common pro-inflammatory cytokines that have been reported as overexpressed in patients with aortic dissection (3-10). Studies found that inflammatory cytokines, including CRP, IL-6, and IL-8, might be associated with the development of acute lung injury in patients with acute TAAD (5,14,18-21), and WBC levels could be elevated in these patients (5,18). In this study, we found that various inflammatory response indicators, including WBC parameters and inflammatory cytokines, were activated in patients with TAAD and significantly higher than in those in patients with ARA. Furthermore, we found that the levels of WBC parameters, including WBC count, neutrophil count, and neutrophil percentage, were higher in patients with acute TAAD than in those with non-acute TAAD, but there were no significant differences in the levels of inflammatory cytokines between acute and non-acute TAAD. These findings indicated that the changes in WBCs and neutrophils were short-lived, tending to return to normal after the acute phase of TAAD, while the alterations in cytokine levels (including those of IL-6, IL-8, TNF-α, CRP, and HIS) were more persistent, remaining activated in the non-acute phase. The time course of changes in WBC and neutrophil parameters was consistent with lung injury occurrence and development, which may indicate that the pulmonary microcirculation is a natural reservoir of leukocytes that is prone to injury during the acute phase of TAAD.

Although the correlations between acute lung injury and systemic inflammatory reactions have been demonstrated repeatedly, the pathogenesis underlying the inflammatory response in patients with aortic dissection is still not completely understood. AAD is a systemic disease, and some organ damage often occurs before surgery, such as heart failure, neurological deficits, and renal, hepatic, and gastrointestinal dysfunction. This organ damage might participate in the development of systemic inflammatory reactions. In 2016, a study found that DAO activity was significantly increased in patients with acute TAAD, that DAO activity was strongly correlated with the levels of some inflammatory cytokines (including IL-6, TNF-α, and CRP), and that DAO activity was negatively correlated with the PaO2-FiO2 ratio (16). These results suggest that intestinal dysfunction plays an important role in the development of the systemic inflammatory response and lung injury in patients with acute TAAD. DAO and iFABP are specifically present in small intestinal mucosal cells, and serum DAO activity and iFABP levels reflect the integrity and degree of damage of the intestinal barrier and are established markers of intestinal barrier dysfunction (22-24). In this study, we found that DAO activity and iFABP concentration were higher in the TAAD group than in the ARA group, while there were no significant differences between the acute and non-acute TAAD subgroups. These findings indicate that the intestinal injury in patients with TAAD occurs and persists for an extended period, continuing after the acute stage. The time course of changes in DAO activity and iFABP concentration was consistent with that of inflammatory cytokines. PGN is a common component of both Gram-positive and Gram-negative bacteria, and it reaches measurable concentrations in serum during bacteremia (25,26). We found that serum PGN levels were increased in patients with TAAD, further suggesting intestinal mucosal damage and barrier dysfunction in these patients, resulting in intestinal bacterial translocation into the blood. In addition, we found that DAO activity and iFABP concentration were significantly correlated with IL-6, IL-8, TNF-α, CRP levels, and PGN concentration, while PGN levels were significantly correlated with levels of IL-6, IL-8, TNF-α, and CRP in the TAAD group. Based on these data, we speculate that the systemic inflammatory response caused by aortic dissection is the cause of intestinal injury, and that bacteremia caused by intestinal injury and intestinal barrier dysfunction may account for the persistence and lack of alleviation of the systemic inflammatory response after the acute stage. The present study also found that PGN concentration was significantly correlated with the PaO2-FiO2 ratio in the acute TAAD subgroup, suggesting that bacteremia caused by intestinal barrier dysfunction and intestinal bacterial translocation may contribute to the occurrence and development of lung injury. Therefore, intestinal injury, although not an initiating insult in pulmonary damage, might enhance lung permeability via an exacerbated inflammatory process.

The present study has several limitations. First, we could not obtain serial blood samples spanning the whole period of the natural progression of aortic dissection from the same patients with TAAD, who almost always require emergency surgery. Therefore, it is difficult to fully determine the dynamic changes in systemic inflammatory responses, intestinal injury, and lung injury and their relationship in the setting of TAAD. Second, although DAO, iFABP, and PaO2-FiO2 ratio are established as excellent indicators of the degree of intestine and lung injury, intestine and lung injury should ideally be evidenced by histological examinations. Nevertheless, this study is an important exploration focusing on the mechanisms and functional implications of systemic inflammatory responses, intestinal injury, and lung injury in patients with TAAD. Importantly, this is the first study to report differences in systemic inflammatory responses, intestinal injury, and lung injury between TAAD and ARA and between acute and non-acute TAAD, which will assist in a more comprehensive understanding of the mechanisms underlying systemic inflammatory responses in patients with TAAD and the resulting damage. It may also inform future studies aimed at optimizing therapeutic strategies for the attenuation of TAAD-related systemic inflammatory responses, regarding to the protection for intestinal barrier function.

Conclusions

In summary, our results highlight the underlying mechanisms and functional implications of intestinal barrier dysfunction in the development of systemic inflammatory responses and lung injury in TAAD. Systemic inflammatory responses in patients with TAAD may lead to lung and intestine injuries, and the latter may be involved in the development of systemic inflammatory responses and lung injury in these patients.

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