Literature DB >> 34840758

Association between serum PGE2 levels and degree of acid-fast bacilli positivity in sputum of pulmonary tuberculosis patients.

Herley Windo Setiawan1,2, Resti Yudhawati1, Irmi Syafaah1.   

Abstract

BACKGROUND: Mycobacterium tuberculosis that infected apoptotic macrophages is triggered by PGE2. Apoptosis suppresses the growth of Mycobacterium tuberculosis bacteria, which is shown in the results of acid-fast bacilli (AFB) in the sputum that becomes a marker of the number of bacteria.
OBJECTIVE: Analyzing the association between serum PGE2 levels and the positivity of AFB in the sputum of tuberculosis patients.
METHODS: A cross-sectional study was carried out from August 2019-July 2020. Serum PGE2 levels and AFB levels in sputum were collected from participants. Data analysis used the Chi-square test and Spearman's correlation with p < 0.05.
RESULTS: The average participants' serum PGE2 levels were 446.37 ± 510.27 pg/ml, with a median value of 216.95 pg/ml. Most participants had normal serum PGE2 levels (62.9%). Most participants had a high positivity of AFB in sputum (58.1%). Analysis of the association between serum PGE2 levels and the degree of AFB positivity in sputum obtained r = -0.036 and p-value = 0.780.
CONCLUSION: There is a weak negative association between serum PGE2 levels and the degree of AFB positivity in sputum but not statistically significant.
© 2021 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd.

Entities:  

Keywords:  Positivity of acid-fast bacilli; Pulmonary tuberculosis; Serum PGE2 levels

Year:  2021        PMID: 34840758      PMCID: PMC8606836          DOI: 10.1016/j.amsu.2021.103008

Source DB:  PubMed          Journal:  Ann Med Surg (Lond)        ISSN: 2049-0801


Introduction

Tuberculosis (TB) is still a global health problem [1]. The increase in TB cases is accompanied by an increase in drug-resistant TB (DR TB) cases. In the Global Tuberculosis Report, WHO reported that 10 million people were suffering from TB, both new and relapsed cases, with 558,000 of whom had DR TB [2]. Indonesia ranks third in the country with the highest TB incidence globally, both new and relapse cases. The number of new and relapsed TB cases in Indonesia in 2017 was 442,172, and 54% of them were confirmed bacteriologically by either acid-fast bacilli (AFB) sputum staining or sputum culture [3]. The pathogenesis of TB is an interaction between Mycobacterium tuberculosis and the host [4]. The process begins with alveolar macrophages and dendritic cells as the first cells facing Mycobacterium tuberculosis bacteria. Macrophages’ response as the mainline in dealing with Mycobacterium tuberculosis infection is influenced by various inflammatory mediators [5]. The failure of macrophages to control the number of Mycobacterium tuberculosis will result in the significant growth of bacteria [6,7]. This condition emphasizes the important role of the host immune system in determining the susceptibility of TB to relapse. Several studies pointed out that Prostaglandin E2 (PGE2) affects macrophages as the main cells in the innate immune system. PGE2 induces apoptosis and inhibits necrosis of macrophages infected with Mycobacterium tuberculosis [5,8,9]. Macrophage apoptosis is reported to reduce the growth rate of Mycobacterium tuberculosis, which is very important in the elimination mechanism of bacteria that infects the lungs, whereas necrosis plays the opposite role [5,8,10]. When the growth of Mycobacterium tuberculosis cannot be inhibited, the number of bacteria will increase. The high number of bacterias is reflected in the degree of phlegm AFB positivity. The higher the value of positivity for AFB in sputum, the greater the number of Mycobacterium tuberculosis bacteria contained in each ml of sputum [11]. The higher the number of bacterias, the easier it is can transmit, broader lung damage, and an increased risk of resistance [12,13]. Based on the facts above, this study further revealed the association between PGE2, which represents the innate immune system, and the degree of phlegm AFB positivity, which represents the number of bacterias. This research is important because no similar study was conducted in humans, so it is hoped that this research could provide further research.

Methods

Participants

Participants in this study were both new and relapsed patients with pulmonary tuberculosis. The inclusion criteria were patients diagnosed with pulmonary tuberculosis [3,14], positive sputum examination results for AFB, aged 21–65 years, who cooperated during the research procedure. Meanwhile, the exclusion criteria included patients with risk factors for immunocompromised (AIDS, malignancy, and systemic lupus erythematosus), patients having received anti-tuberculosis drug therapy for their current illness, patients taking non-steroidal anti-inflammatory drugs and/or corticosteroids in the past week.

Ethical clearance

Participants and their families filled out the consent form before the study. Participants filled out the consent form consciously and without coercion. This study received ethical approval based on the Declaration of Helsinki and obtained the registry of research at the Health Research Ethics Committee in the Hospital.

Study design

A cross-sectional study was carried out from August 2019–July 2020. The number of participants in this study was 62 patients that were obtained using Ronald Fisher's classic z transformation formula. The sample collection used a consecutive sampling technique (Fig. 1). Serum PGE2 levels and levels of AFB in sputum were taken from the participants. This study report is by the Strengthening the Reporting of Cohort Studies in Surgery (STROCSS) 2019 guideline [15].
Fig. 1

Participant requitement process.

Participant requitement process.

Measurement of serum PGE2 level

Serum PGE2 level is the total concentration of PGE2 in the blood of pulmonary tuberculosis patients. This examination was carried out by taking 3–5 ml of the patient's venous blood and analyzed using the Elisa Kit PGE2 (pg/ml). Serum PGE2 level is categorized into high if the value is more than 400 pg/ml, normal if the value is 200–400 pg/ml, and low if the value is less than 200 pg/ml [16].

Acid-fast bacilli test

Sputum examination was conducted to determine the degree of the participant's AFB positivity. Sputum collection for participants is carried out by the patient independently in the morning [17] which the participant gets an explanation form a pulmonary specialist regarding effective deep breathing and coughing techniques [18]. The sputum is put into a tube that has been prepared previously and then taken to the laboratory for analysis. The examination of AFB in the participant's sputum used the acid-fast staining method (Ziehl Nielssen) or the rapid molecular test of sputum with the GeneXpert machine [19]. The degree of phlegm AFB positivity was assessed based on the International Union Against Tuberculosis Lung Disease (IUATLD) standards which were categorized into 2: low (1+ and scanty) and high (2+ and 3+) [19,20].

Statistical analysis

The analysis in this study used descriptive analysis and bivariate analysis. Descriptive analysis included the presentation of the results descriptively using the distribution table, mean, median, standard deviation, maximum value, and minimum value. Meanwhile, bivariate analysis was used to assess the association between two variables. The association between variables was analyzed using the Chi-Square test and assessed the association strength using the Spearman correlation test. The analysis was declared significant if p < 0.05. The analysis was assisted by IBM SPSS Statistics software version 21.0 (IBM Corp., Armonk, NY, USA).

Results

Characteristic of participant

Most participants were male who was 43.37 ± 12.58 years old. Meanwhile, the median of participants’ age was 44.5 years, with the lowest age being 21 years and the highest being 64 years. Some patients had a smoking habit (56.5%) and comorbidity of diabetes mellitus (32.3%). A total of 37 participants were new tuberculosis patients and the rest were relapsed, tuberculosis patients. Most participants had a body mass index (BMI) in the skinny category as much as 53.2% (Table 1). The average BMI value was 19.46 ± 4.05 kg/m2, with a value range of 14.20–38.28 kg/m2.
Table 1

Characteristic of participant.

Variablen (%)
Sex
 Male36 (58.1)
 Female26 (41.9)
Education
 Elementary School8 (12.9)
 Junior High School12 (19.4)
 Senior High School34 (54.8)
 College7 (11.3)
 Not attending school1 (1.6)
History of Diabetes Mellitus
 Yes20 (32.3)
 No42 (67.7)
History of Tuberculosis Treatment
 New case37 (59.7)
 Relapse25 (40.3)
Smoking Habit
 Smoking35 (56.5)
 No smoking27 (43.5)
Degree of Acid-Fast Bacilli Positivity
 Low26 (41.9)
 High36 (58.1)
Serum PGE2 Level
 Low9 (14.5)
 Normal39 (62.9)
 High14 (22.6)
Body Mass Index
 Skinny (<18.5 kg/m2)33 (53.2)
 Normal (18.5–25.0 kg/m2)24 (38.7)
 Fat (>25.0 kg/m2)5 (8.1)
Characteristic of participant.

Distribution of serum PGE2 levels in tuberculosis patients

Most participants had normal serum PGE2 levels (62.9%; Table 1). The average participants had serum PGE2 levels of 446.37 ± 510.27 pg/ml, with a median value of 216.95 pg/ml. The lowest and highest value of the participants’ serum PGE2 levels were 191.00 pg/ml and 2374.00 pg/ml, respectively. The serum PGE2 levels of smoking and non-smoking participants was 228.80 (191.0–2,3374.0) pg/ml and 214.40 (198.3–1724.0) pg/ml, respectively. Most serum PGE2 levels of smoking participants were normal (50%), while the serum PGE2 levels of non-smoking participants were mostly normal (78%; p = 0.053). The median value of serum PGE2 levels for participants with and without diabetes mellitus was 217.30 (191.0–1986.0) pg/ml and 216.80 (193.0–2374.0) pg/ml, respectively. The value of serum PGE2 levels of participants with and without diabetes mellitus were 45% and 71%, respectively, indicating that most participants had normal values (p = 0.118; Table 2).
Table 2

Distribution of serum PGE2 levels in tuberculosis patients.

VariableSerum PGE2 Levels
p
LowNormalHigh
Pulmonary Tuberculosis
 New case6 (16)23 (62)8 (22)0.292
 Relapse case3 (12)16 (64)6 (24)
Diabetes mellitus
 Yes4 (20)9 (45)7 (35)0.118
 No5 (12)30 (71)7 (17)
BMI
 Skinny1 (3)24 (73)8 (24)0.058
 Normal7 (29)12 (50)5 (21)
 Fat1 (20)3 (60)1 (20)
Smoking
 Yes6 (18)17 (50)11 (32)0.053
 No3 (11)22 (78)3 (11)

Abbreviation: BMI = body mass index.

Distribution of serum PGE2 levels in tuberculosis patients. Abbreviation: BMI = body mass index. Most of the participants’ serum PGE2 levels were normal in both groups of participants with a new diagnosis of pulmonary tuberculosis (62%) and relapsed (64%; p = 0.292). The median value of serum PGE2 levels for participants diagnosed with new pulmonary tuberculosis was 215.70 (191.0–1724.0) pg/ml and participants diagnosed with relapsed pulmonary tuberculosis was 224.40 (193.2–2374.0) pg/ml. Participants' serum PGE2 levels that were categorized by BMI were mostly normal, with 73% of skinny participants, 50% of normal participants, and 60% of fat participants (p = 0.058; Table 3). The median value of serum PGE2 levels of participants with BMI in the skinny category was 222.60 (194.3–1986.0) pg/ml, normal was 210.30 (191.0–2374.0) pg/ml, and fatwas 216.40 (199.0–1497.0) pg/ml.
Table 3

Distribution of positivity of acid-fast bacilli in sputum of tuberculosis patients.

VariableDegree of Acid-Fast Bacilli Positivity
p
Low (%)High
Pulmonary Tuberculosis
 New case12 (32)25 (68)0.065
 Relapse case14 (56)11 (44)
Diabetes Mellitus
 Yes7 (35)13 (65)0.455
 No19 (45)23 (55)
BMI
 Skinny15 (45)18 (55)0.561
 Normal10 (42)14 (58)
 Fat1 (20)4 (80)
Smoking
 Yes15 (45)19 (56)0.798
 No11 (39)17 (61)

Abbreviation: BMI = body mass index.

Distribution of positivity of acid-fast bacilli in sputum of tuberculosis patients. Abbreviation: BMI = body mass index.

Distribution of positivity of acid-fast bacilli in sputum of tuberculosis patients

Most participants had a high degree of AFB positivity in sputum as much as 58.1% (Table 1). Most participants who were diagnosed with new cases of pulmonary tuberculosis had a high degree of AFB positivity (68%). Meanwhile, most participants diagnosed with relapsed pulmonary tuberculosis had a low positivity degree (56%; p = 0.065). Some participants had a high degree of AFB positivity in participants with and without a history of diabetes mellitus of 65% and 55%, respectively (p = 0.455). Participants' BMI was categorized into 3, namely skinny, normal, and fast, in which some participants had a high degree of AFB positivity (p = 0.561). Most smoking (56%) and non-smoking (61%) participants had high positivity of AFB (p = 0.798; Table 3).

Association between serum PGE2 levels and positivity of acid-fast bacilli in sputum of tuberculosis patients

The results showed that most participants with low (89%) and high (71%) serum PGE2 levels had a high positivity of AFB in sputum as much as 89%. Meanwhile, participants with normal serum PGE2 levels had a low positivity degree of AFB in sputum as much as 54% (p = 0.036). The strength of the association between serum PGE2 levels and the degree of AFB positivity in sputum obtained r = −0.036 and p-value = 0.780 (Table 4).
Table 4

Association between PGE2 levels and positivity of acid-fast bacilli in the sputum of tuberculosis patients.

VariableTuberculosis Positivity
parpb
LowHigh
PGE2 Levels
Low1 (11)8 (89)0.036−0.0360.780
Normal21 (54)18 (46)
High4 (29)10 (71)

Note: pa = Chi-square test; pb = Spearman's correlation test.

Association between PGE2 levels and positivity of acid-fast bacilli in the sputum of tuberculosis patients. Note: pa = Chi-square test; pb = Spearman's correlation test.

Discussion

PGE2 is a derivative of arachidonic acid produced by various inflammatory cells, especially macrophages. PGE2, as an inflammatory mediator, plays a role in regulating various cell functions, namely macrophages, T cells, etc. In addition, PGE2 plays a role in various body functions such as blood pressure regulation, temperature regulation, gastric protection, and childbirth [21]. Under various conditions such as changes in environmental temperature, hunger conditions, stress, PGE2 will be produced so that levels in the body will rise and fall in various ways [22]. Schoenberger et al. reported an increase in serum PGE2 levels in patients with diabetic retinopathy [23]. A study conducted by Lo et al. showed that the increase in serum PGE2 levels was due to the upregulation of the cyclooxygenase-2 (COX2) enzyme in patients with diabetes mellitus [24]. Kumar et al. reported differences in plasma PGE2 levels in TB patients compared to TB-DM [16]. These results are inconsistent with various studies that reported increased levels of PGE2 in smokers. Amadio et al. reported an increase in PGE2 production in smokers due to the modulation of expression of tissue factors exposed to cigarette smoke [25]. Chen et al. in their study also reported the role of cigarette smoke in increasing PGE2 production [26]. The condition obtained in this study seemed to occur because of the patient's experience factor. In patients with relapse cases, the experience of suffering from TB in the past will make the patient who has a cough immediately come to the health facility. Meanwhile, new case patients ignore the cough complaint that leads to accompanying complaints such as weight loss, hemoptysis, or fever. When these accompanying complaints occur, the course of TB disease would be long enough to increase the number of bacterias [1]. The profile of serum PGE2 levels showed that the average participants had 446.23 pg/ml, with a standard deviation of 510.27 pg/ml. According to some literature, normal serum PGE2 levels range from 200 to 400 pg/ml [16]. PGE2 is a derivative of arachidonic acid produced mainly by inflammatory cells to face invading pathogens from outside. The effect of PGE2 will trigger apoptosis of macrophages infected with Mycobacterium tuberculosis [4]. Macrophage apoptosis will have an elimination effect because Mycobacterium tuberculosis bacteria can be destroyed. PGE2 also suppresses macrophage necrosis which can lead to bacterial dissemination. Increased levels of PGE2 are associated with a decrease in the number of bacteria in the lung [7]. The negative association between serum PGE2 levels and the degree of phlegm AFB positivity is by a study conducted by Dietzold and Amaral. Dietzold et al. reported that high levels of PGE2 and low levels of LXA4 suppress the growth of Mycobacterium tuberculosis [7]. Amaral et al. also reported that PGE2 is associated with macrophage apoptosis in vitro. Apoptotic macrophages infected with Mycobacterium tuberculosis will increase the elimination of these bacterias [4]. The two studies above reported a significant association between PGE2 and the growth of Mycobacterium tuberculosis. The statistical analysis results of this study showed that the association between serum PGE2 levels and the degree of AFB positivity was not statistically significant. The main difference between this study and the two studies above is that both were carried out on mice and in vitro, whereas this study was conducted on pulmonary TB patients with various complications and uncontrollable comorbidities. The results of this study can be used as consideration for conducting further research on the predictor factors for the positivity of AFB in pulmonary TB patients. The use of PGE2 together with LXA4 is expected to be able to assist clinicians in predicting the level of AFB positivity in pulmonary TB patients with specific chest X-ray images but difficulty in expectorating phlegm. In addition, in the future study it can be considered to analyze the comparison of PGE2 in TB patients, smokers patients, smokers with tuberculosis, etc. Nevertheless, this study has several limitations. First, extreme serum PGE2 levels were found in some research subjects. This can be caused by various factors that can increase PGE2 levels that cannot be controlled. Second, this study only examined PGE2 levels in TB patients without comparing them with PGE2 levels in healthy persons, so it cannot be used as a predictor factor for the degree of positivity of AFB with sputum.

Conclusion

The average age of new and relapsed pulmonary TB patients is 43.37 years, mostly male, have a high school education, have a smoking habit, have a low BMI, and have no history of DM. The median serum PGE2 level of new and relapsed pulmonary TB patients was 216.95 pg/ml. The majority of new pulmonary TB patients have a high degree of positivity for AFB in sputum, but relapsed pulmonary TB patients have a low degree of positivity for AFB. This study finds a weak negative association between serum PGE2 levels and the degree of phlegm AFB positivity but not statistically significant.

Please state any sources of funding for your research

None.

Ethical approval

We have conducted an ethical approval base on Declaration of Helsinki at Ethical Committee in Dr. Soetomo General Academic Hospital, Surabaya, Indonesia.

Consent

Written informed consent was obtained from the patient.

Author contribution

All authors contributed toward data analysis, drafting and revising the paper, gave final approval of the version to be published and agree to be accountable for all aspects of the work.

Registration of research studies

Name of the registry: Health Research Ethics Coommitee in the Dr. Soetomo General Academic Hospital, Surabaya, Indonesia. Unique Identifying number or registration ID: 1355/KEKP/VII/2019. Hyperlink to your specific registration (must be publicly accessible and will be checked):-.

Guarantor

Resti Yudhawati.

Funding

Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.

Provenance and peer review

Not commissioned, externally peer-reviewed.

Declaration of competing interest

The authors declare that they have no conflict of interest.
  23 in total

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Review 7.  Duality of lipid mediators in host response against Mycobacterium tuberculosis: good cop, bad cop.

Authors:  Jillian Dietzold; Archana Gopalakrishnan; Padmini Salgame
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Authors:  Nathella Pavan Kumar; Kadar Moideen; Arul Nancy; Vijay Viswanathan; Basavaradhya S Shruthi; Sivakumar Shanmugam; Syed Hissar; Hardy Kornfeld; Subash Babu
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Authors:  Michael E Murphy; Patrick P J Phillips; Carl M Mendel; Emily Bongard; Anna L C Bateson; Robert Hunt; Saraswathi Murthy; Kasha P Singh; Michael Brown; Angela M Crook; Andrew J Nunn; Sarah K Meredith; Marc Lipman; Timothy D McHugh; Stephen H Gillespie
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