- Journal List
- Cureus
- v.15(9); 2023 Sep
- PMC10604499
As a library, NLM provides access to scientific literature. Inclusion in an NLM database does not imply endorsem*nt of, or agreement with, the contents by NLM or the National Institutes of Health.
Learn more: PMC Disclaimer | PMC Copyright Notice
Cureus. 2023 Sep; 15(9): e46095.
Published online 2023 Sep 27. doi:10.7759/cureus.46095
PMCID: PMC10604499
PMID: 37900420
Monitoring Editor: Alexander Muacevic and John R Adler
Sudipta D Baruah,1 Satyajit Mitra,2 Bishwajeet Saikia,3 Joydev Sarma,2 and Monalisa Nath2
Author information Article notes Copyright and License information PMC Disclaimer
Abstract
Introduction
Columnar lined epithelium (CLE) of the esophagus holds particular importance in diagnosing Barrett's esophagus (BE). In Asia, the prevalence of BE ranges from 0.06% to 6.2%. In India, prevalence estimates vary from 2.6% to 23%. The frequency of esophageal adenocarcinoma has also been observed to be increasing alarmingly over the past few decades. The length of CLE as a criterion for diagnosing BE is the subject of considerable debate. Changes in CLE length among different age groups may exist. Our study aims to measure the length of CLE, or the distance between the angle of His and the Z Line (AZ distance), in normal individuals from Northeast India, and to analyze its variation across different age groups.
Materials and methods
The study was conducted in the Department of Anatomy and the Department of Forensic Medicine and Toxicology at Gauhati Medical College, Guwahati, Assam, India, during the period 2017-2019. Once opened, each specimen was laid flat on a board. The distance between the A and Z lines was measured using a pair of vernier calipers. This distance was recorded as the AZ distance in millimeters (mm).
Results
The mean AZ Distance was found to be 12.4 ± 5.3 mm. A significant correlation between age and AZ distance was observed.
Conclusion
Our present study suggests that the length of the CLE increases with age. This observation offers an opportunity to revisit or revise the diagnostic criteria based on CLE length, taking into account the age of the individual.
Keywords: lower end of esophagus, anatomy, histology, columnar lined esophagus, esophagus
Introduction
In the mid-1930s, the lower end of the esophagus and the gastric cardia grabbed the attention of surgeons. The reason for this increased attention was the presence of numerous anatomical transitions, the most significant of which is the stratified to columnar transition of the epithelium. This columnar lined epithelium (CLE) of the esophagus is of particular importance while diagnosing Barrett’s esophagus (BE). People with gastroesophageal reflux disease (GERD) are at high risk of developing BE [1]. In Asia, excluding Japan, the prevalence of BE ranges from 0.06% to 6.2%[1];in Japan, the prevalence ranges from 19.9% [2]to 43%[3]. The prevalence in India is estimated to range from 2.6% to 23%[4,5]. The frequency of esophageal adenocarcinoma, of which BE is often the precursor, has also been seen to increase alarmingly over the past few decades [6,7].
Materials and methods
Relevant anatomy of the gastroesophageal junction
As the esophagus joins the stomach, its lumen becomes continuous. This part of the esophagus, the abdominal esophagus (0.5-2.5 cm) [8], is intraperitoneal and meets the cardiac end of the stomach, creating the gastroesophageal junction (GEJ).
Definition of CLE
Anatomical Examination
Externally, this is marked by the cardiac notch of the stomach or the angle of His (A). The A corresponds to the anatomical GEJ [9]. On gross anatomical examination, the squamocolumnar junction is visible internally as a distinct jagged margin, which is popularly called the Z line [2]. Until this point, the proximal esophagus is lined by a stratified squamous non-keratinised epithelium. The Z line is usually a little distance proximal to the A [10]. This distance of the Z line from the A, which can be termed the AZ distance, represents the terminal part of the esophagus, lined by simple columnar epithelium, and thus corresponds to the CLE (Figures (Figures1,1, ,22).
Figure 1
Open in a separate window
A specimen of esophagus and stomach selected for the research.
Figure 2
Open in a separate window
A cut specimen of esophagus and stomach showing the gross anatomical landmarks (stretched on the right side).
Endoscopic Examination
During upper gastrointestinal endoscopy, the Z line is visible as a junction between the pale pearly colored squamous epithelium and the salmon-colored columnar epithelium. The GEJ is usually identified as a pinch at the distal end of the esophagus, coinciding with the most proximal appearance of the gastric rugal folds. This point marks the beginning of the stomach and its distance from the Z line conventionally corresponds to the CLE [4,11]. Endoscopically the AZ distance/length of CLE can be measured by subtracting the distance of the incisor to the squamocolumnar junction (Z line) from the distance of the incisor to the gastroesophageal junction (Figure (Figure33).
Figure 3
Open in a separate window
Endoscopic landmarks for determining the CLE.
Endoscopic picture provided by Dr. PKD phu*kan, General Surgeon.
CLE:columnar lined epithelium.
The distribution of the AZ distance/length of CLE is a very significant and well-established criterion for diagnosing BE in clinical practice. The length of CLE as a criterion for diagnosing BE surrounds much controversy and has been kept arbitrary. The CLE can be expected to have a length of up to 2 cm in normal individuals [12,13]. Later on, more views came in where the acceptable value of CLE length to be diagnosed as BE was kept arbitrarily at >3 cm [14]. There were many more studies challenging the previous ones, creating controversies that still surround the normal CLE length.It may also be worth mentioning here that there may be changes in the CLE length among the different age groups that can be very critical in diagnosing an abnormal proximal shift in the Z line, indicative of BE. Therefore, with all of these arbitral values that surround the CLE length, our study attempted to measure the length of the CLE/AZ distance in normal individuals from North East India and to analyze its variation across different age groups.
The study was conducted in a tertiary care institution during the period of 2017-2019. Ethical clearance was obtained from the Institutional Ethics Committee of Gauhati Medical College and Hospital (approval MC/190/2007/Pt-1/EC/134). The specimens were collected during the routine dissection of cadavers in the Department of Anatomy, and consecutive specimens were obtained from the autopsy. A total of 50 specimens were collected, of which 32 were from male and 18 were from female cadavers. The inclusion and exclusion criteria are given in Table Table11.
Table 1
Inclusion and exclusion criteria.
Inclusion Criteria | Exclusion Criteria |
Road traffic accident without thoracoabdominal trauma | Death due to poisoning |
Death due to cardiorespiratory failure | Evidence of previous gastrointestinal surgery |
Death due to cerebral stroke | Road traffic accident involving thorax and abdomen |
Death due to any other cause that does not affect the esophagus and stomach | History of any condition that could possibly affect the esophagus and stomach like gastroesophageal reflux disease, frequent gastritis, acid peptic disease, etc. |
Open in a separate window
The autopsies were performed within 48 hours after death. The stomach and the esophagus were preserved by placing them in a container with 10% formalin. The lower two-thirds of the esophagus and the stomach were removed for the purpose of the study. The stomach was cut open from the pylorus along the greater curvature. The incision was extended to the esophagus [15]. Once opened, the specimen was laid flat on a board. The angle of His (A) was noted as the point of deepest indentation between the esophagus and the stomach. The Z line was noted as the zig-zag line demarcating the junction between the non-keratinized stratified squamous epithelium above and the simple columnar epithelium below. The distance between the A and the Z line was measured by using a pair of vernier calipers. This distance was noted as AZ in millimeters (mm) [16].
Statistical tools
The data wereanalyzed to find out the mean, standard deviation, and standard error of the mean. The age of the individual was obtained from the death certificate. The correlation of the length of the columnar-lined esophagus with age was analyzed using Pearson’s product-moment correlation. IBMSPSSStatistics for Windows, Version 25 (Released 2017; IBM Corp., Armonk, New York, United States) was used for the analysis of data.
Results
Of the 50 specimens that were studied, 18 specimens were females and 32 were males. The data werecollected in age groups spanning 20 years each(Table 2).
Table 2
Age-wise and gender-wise distribution of the specimen to study the morphology and histology of the gastroesophageal junctions.
Age Groups | Male | Female |
0-20 years | 5 | 2 |
20-40 years | 15 | 9 |
40-60 years | 9 | 6 |
60 years and above | 3 | 1 |
Total | 32 | 18 |
Grand total | 50 |
Open in a separate window
The mean and standard deviation of the AZ distance for each age group are shown in Table Table33.
Table 3
Mean and standard deviation (in mm) of the AZ distance in various age groups.
AZ distance: distance from the angle of His to the Z line.
Age group | Mean (mm) |
0-20 | 5.3666 ± 5.5174 |
20-40 | 12.636 ± 5.025 |
40-60 | 13.72 ± 3.724 |
Above 60 | 17.025 ± 1.9972 |
Open in a separate window
The mean AZ distance was found to be 12.4 mm with a standard deviation of 5.3 mm. The standard error of the mean was found to be 0.75 mm.For testing the correlation between age and AZ distance, Pearson’s product-moment correlation measure was used.
The null hypothesis is as follows:H0: There is no correlation between age and AZ distance.
The value of the correlation coefficient has been found to be 0.3400952 and the p-value of the test is 0.0156 < 0.05, which is significant at a 5% level of significance. So, we reject H0 at a 5% level of significance and conclude that there is a significant correlation between age and AZ distance. In graphical representation using a line graph with a trendline, a clear upward trend is evident in the length of the AZ distance with age (Figure (Figure44).
Figure 4
Open in a separate window
Line graph with a trendline showing the AZ distance (in mm) against age.
Discussion
Existing literature provides abundant data on the lower end of the esophagus. With an increased understanding of the pathological conditions affecting the lower end of the esophagus that are considered precancerous, this has become one of the most clinically significant areas in the body. Yet, the details and the precise anatomy of the region are not very clear. Several authors have studied the position of the Z line in relation to the GEJ (A) and the AZ distance corresponding to the CLE in normal subjects. In their study, Creamer et al. found the AZ distance to be in the range of 14-32 mm [17]. Bonibeck et al. found it to be in the range of 4-20 mm [16]. Liebermann-Meffert recorded a range of 9-21 mm [15], while Takubo et al. recorded a range of 0-10 mm [18]. In our present study, we found the AZ distance to be in the range of 0-20.2 mm.
Similarly, there was much variation in the mean of the AZ distance/length of CLE according to various studies. Studies based on autopsy found the length to be in a range from 10.4 mm [5]to 11 mm [6]. Simultaneously, radiology and endoscopic studies found this length to be 20 mm [7]and 15 mm [8], respectively. In our study, we found the mean AZ distance to be 12.4 mm with a standard deviation of ±5.3 mm, corroborating mostly with the previous cadaver-based studies.
The AZ distance corresponds to the length of the CLE and is crucial in defining BE. The length of CLE holds a significant correlation with intestinal metaplasia. Some authorities opine that even though long-segment BE is at a higher risk of developing carcinoma, a significant number of carcinomas are also seen to have developed in short-segment BE patients. They have attributed this to the imprecise measurement of BE in endoscopic procedures owing to the difficulty in identifying the exact point of transition from the esophagus to the stomach. At times this has also led to disagreement among endoscopists about the presence or absence of BE in the same patient [8]. An endoscopic study done on patients with a mean age of 48.15±10.90 years found that the patients with intestinal metaplasia had a CLE with a mean±SD length of 3.0±1.26 cm, while patients without metaplasia had a CLE length of 1.8±0.59 cm (p=0.001) [1]. In our study, the maximum length of CLE in normal subjects above 60 years was found to be 1.7± 1.99, which, therefore, falls well within the normal anatomical limit. Moreover, if we consider the length of the CLE in normal subjects, there was a mild increase in the measurements found during endoscopy when compared to cadaveric-based studies [5,6,8]. This discrepancy might represent a change in post-mortem anatomy or perhaps is due to the fact that the A, which is the true anatomical GEJ, is not possible to determine from the luminal side of the esophagus. Instead, the first appearance of gastric folds is usually taken as a landmark that may not coincide exactly with the A or the anatomical GEJ. Thus, defining the A, the true anatomical GEJbecomes difficult during routine endoscopic procedures. Additionally, even though this difference in the AZ distance/length of CLE found in our cadaveric study compared to previous endoscopic studies is minimal, it can be significant while defining the actual length of the CLE. This difference in length may be critical while diagnosing BE and perhaps leaves scope to recognize and refine the diagnostic accuracy in determining the critical length of actual CLE based on the true anatomical GEJ. Further, in our study, it was seen that there was a significant correlation between the AZ distance/anatomical CLE and the age of the individual. This can be of utmost importance while diagnosing BE in elderly patients.
Limitations of our study
A cadaveric study like ours might not be representing the anatomy of the gastroesophageal junction in live subjects. Correlating BE through AZ distance in cadavers lacks predictors like gastro-oesophageal reflux, which are usually considered in studies on live subjects. Correlating the study with the histology of the CLE can establish further evidence. With a bigger sample size, the study can have a better impact. We were not able to measure the entire length of the esophagus for its correlation with the AZ distance. This is one point where the study can be improved upon.
Conclusions
An accurate description and definition of the columnar-lined esophagus in the lower end is of paramount importance. The diagnosis of BE relies heavily on the proximal shift of the Z line from its normal anatomical position. The anatomical GEJ may not correspondto endoscopically measured GEJ. Therefore, the endoscopically measured CLE does not represent the true anatomical CLE or the AZ distance. Our present study suggests that the length of the CLE increases with age. This observation of ours creates a scope to revise/revisit the diagnostic criteria based on CLE length in accordance with the age of the individual.
Acknowledgments
Endoscopic gastroesophageal junction photo was provided by Dr. PKD phu*kan, General Surgeon.
Notes
The authors have declared that no competing interests exist.
Human Ethics
Consent was obtained or waived by all participants in this study. Institutional Ethics Committee of Gauhati Medical College and Hospital issued approval MC/190/2007/Pt-1/EC/134
Animal Ethics
Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.
References
1. Prevalence and risk factors for Barrett’s esophagus in patients with GERD in northern India; do methylene blue-directed biopsies improve detection of Barrett’s esophagus compared the conventional method? Wani IR, Showkat HI, Bhargav DK, Samer M. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208931/ Middle East J Dig Dis. 2014;6:228–236. [PMC free article] [PubMed] [Google Scholar]
2. Prevalence of Barrett's esophagus in Korea. Kim JY, Kim YS, Jung MK, et al. J Gastroenterol Hepatol. 2005;20:633–636. [PubMed] [Google Scholar]
3. Prevalence and risk factors of Barrett's esophagus in Korea. Kim JH, Rhee PL, Lee JH, et al. J Gastroenterol Hepatol. 2007;22:908–912. [PubMed] [Google Scholar]
4. Prevalence of short segments of specialized columnar epithelium in distal esophagus: association with gastroesophageal reflux. Dhawan P, Alvares J, Vora I. https://www.researchgate.net/profile/Shobna-Bhatia/publication/11847985_Prevalence_of_short_segments_of_specialized_columnar_epithelium_in_distal_esophagus_association_with_gastroesophageal_reflux/links/54114dbb0cf2f2b29a412633/Prevalence-of-short-segments-of-specialized-columnar-epithelium-in-distal-esophagus-association-with-gastroesophageal-reflux.pdf. Indian J Gastroenterol. 2001;20:144–147. [PubMed] [Google Scholar]
5. Barrett's esophagus. Amarapurkar AD, Vora IM, Dhawan PS. https://pubmed.ncbi.nlm.nih.gov/9866904/ Indian J Pathol Microbiol. 1998;41:431–435. [PubMed] [Google Scholar]
6. Adenocarcinoma in Barrett’s esophagus: a new epidemic? Haggitt R. Hum Pathol. 1992;23:475–476. [PubMed] [Google Scholar]
7. Esophageal cancer trends and risk factors. Blot WJ. https://pubmed.ncbi.nlm.nih.gov/8042037/ Semin Oncol. 1994;21:403–410. [PubMed] [Google Scholar]
8. John Hopkins Gastroenterologists. Barrett’s Esophagus [Internet]. Barrett’s Esophagus. 2001202128. https://www.hopkinsmedicine.org/gastroenterology_hepatology/_pdfs/esophagus_stomach/barretts_esophagus.pdf
9. Robert S. London, U.K.: Churchill Livingstone Elsevier; 2008. Gray’s Anatomy: The Anatomical Basis of Clinical Practice, 40 ed. [Google Scholar]
10. The cardia: esophageal or gastric? Critical reviewing the anatomy and histopathology of the esophagogastric junction. Lenglinger J, See SF, Beller L, et al. Acta Chir Iugosl. 2012;59:15–26. [PubMed] [Google Scholar]
11. Diagnosis and management of Barrett's esophagus for the endoscopist. Garud SS, Keilin S, Cai Q, Willingham FF. Therap Adv Gastroenterol. 2010;3:227–238. [PMC free article] [PubMed] [Google Scholar]
12. Definition of Barrett's oesophagus. Van Eyken P. https://pubmed.ncbi.nlm.nih.gov/10907312/ Acta Gastroenterol Belg. 2000;63:10–12. [PubMed] [Google Scholar]
13. Endoscopic definitions of esophagogastric junction regional anatomy. Rutgeerts PGP. Gastrointest Endosc. 2000;51:586–592. [PubMed] [Google Scholar]
14. Barrett's esophagus: comparison of benign and malignant cases. Skinner DB, Walther BC, Riddell RH, Schmidt H, Iascone C, DeMeester TR. Ann Surg. 1983;198:554–565. [PMC free article] [PubMed] [Google Scholar]
15. Muscular equivalent of the lower esophageal sphincter. Liebermann-Meffert D, Allgöwer M, Schmid P, Blum AL. https://pubmed.ncbi.nlm.nih.gov/81791/ Gastroenterology. 1979;76:31–38. [PubMed] [Google Scholar]
16. Muscular anatomy of the gastroesophageal junction and role of phrenoesophageal ligament: autopsy study of sphincter mechanism. Bombeck CT, Dillard DH, Nyhus LM. Ann Surg. 1966;164:643–654. [PMC free article] [PubMed] [Google Scholar]
17. Further observations on the gastro-oesophageal junction. CR B, HA GK, PI JW. Thorax. 1959;14:132–137. [PMC free article] [PubMed] [Google Scholar]
18. The normal anatomy around the oesophagogastric junction: a histopathologic view and its correlation with endoscopy. Takubo K, Aida J, Sawabe M, Arai T, Kato H, Pech O, Arima M. Best Pract Res Clin Gastroenterol. 2008;22:569–583. [PubMed] [Google Scholar]
Articles from Cureus are provided here courtesy of Cureus Inc.