The Biologic Basis of Hernia Formation



Status:Completed
Conditions:Gastrointestinal
Therapuetic Areas:Gastroenterology
Healthy:No
Age Range:18 - Any
Updated:5/16/2018
Start Date:August 2007
End Date:October 2011

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The study will examine potential biological and genetic mechanisms leading to hiatal and
paraesophageal hernia formation in predisposed individuals. It is expected that these
patients will have defects in the normal production and maturation of collagen and other
connective tissue proteins, thus leading to weakness in the diaphragm that may allow for
spontaneous herniation. Comparison of tissue and blood samples from these patients (study
group) will be made to those from individuals undergoing lower esophageal surgery who have
not developed a concurrent hernia (i.e. esophageal myotomy for achalasia and laparoscopic
gastric bypass or laparoscopic adjustable gastric banding for morbid obesity - control
group).

Diaphragmatic herniation is a common medical problem characterized by protrusion of the
abdominal viscera directly through (95% of cases), or adjacent to (5% of cases), the
esophageal hiatus. Individuals suffering from these so-called hiatal and paraesophageal
hernias experience symptoms such as regurgitation, heartburn, early satiety, and in extreme
cases, respiratory compromise or visceral strangulation and ischemia. Unless the hernia is
small, these symptoms are generally refractory to medical management and require surgical
correction, with approximately 40,000 antireflux surgeries being performed each year in the
United States. The hernia repair procedure, which may be performed in either a laparoscopic
or open fashion, involves reduction of the intrathoracic viscera back into the abdominal
cavity and closure of the diaphragmatic defect. Generally, this closure of the hernia can be
accomplished primarily, using nonabsorbable suture to approximate the edges of the defect.
Unfortunately, the recurrence rate for this type of repair is unacceptably high and ranges
from 10-40%. Furthermore, in the instance of a particularly large hernia, the edges of the
defect may be too far apart to be primarily brought together, necessitating the use of other
strategies such as relaxing incisions or patches to bridge the gap. Although the precise
recurrence rates of these complex repairs is not clear, it is expected that they are even
higher that for those diaphragmatic hernias that can be closed primarily.

The genetic and biologic factors that predispose individuals to forming hernias are not well
understood. Several smaller series have suggested that ventral and inguinal hernia formation
may be due to weakness of the abdominal wall, possibly secondary to defects in collagen
deposition and metabolism. Certain studies have shown higher ratios of Type III collagen
(immature) to Type I collagen (mature), at both the protein and mRNA level, in patients with
abdominal hernias as compared to those without. Furthermore, other reports indicate that
these differences in the levels of mature collagen might be due to underlying differences ion
the expression of certain matrix metalloproteinase (MMPs), which are largely responsible for
collagen remodeling. MMPs -1, -2, -3, -9, and -13 have been shown to be upregulated in
connective tissue injury, and alterations in both MMP-2 and fibrillar collagen can interfere
with normal wound healing. Furthermore, Bellon et. al. have shown an overexpression of MMP-2
in fibroblasts in patients with direct inguinal hernias, and Zheng's group detected MMP-13
overexpression in tissue samples from patients with recurrent inguinal hernias. So far, no
studies have addressed the role of collagen deposition and MMPs in the formation of hiatal
and paraesophageal hernias. Preliminary work at our institution has, however, shown a greater
than 50% reduction in the elastin content of the phrenoesophageal and gastrohepatic ligaments
("PEL" and "GHL", respectively) of those patients with a hiatal hernia compared to those
without herniation. Additionally, the elastic fibers in the PEL and GHL frequently displayed
fragmentation and distortion despite the lack of a visible inflammatory response. (J.A. Curci
and N.J. Soper, unpublished results) Nevertheless, neither our early work, nor any of the
studies from outside institutions have looked at ways of screening patients (i.e. via blood
sampling) to detect those at a higher risk for such hernia occurrence. Currently, new
MMP-inhibitory drugs are being studied as methods to potentially block or slow the
development of other MMP-dependent conditions such as abdominal aortic aneurysm (AAA). Along
these lines, if patients with a genetic/biologic predisposition to hernia formation could be
readily identified, then this presents a potential point of medical intervention in
preventing future hernia development.

Research procedures:

Patients to be enrolled in the study will be standard referrals to our group from primary
care physicians or other specialists who feel that surgical correction of a diaphragmatic
hernia or achalasia is necessary. Additionally, patients referred to our practice for weight
reduction surgery will also be considered eligible for enrollment.

Consent to participate in the study will occur at the time of consent to the surgical
procedure and will be obtained by the PI and other attending surgeons within the minimally
invasive surgery group. This will occur in the surgeon's office/clinic, or in the hospital if
the patient is an in-house consult, several days to weeks prior to the scheduled surgery.

Following the informed consent process, patients will be appropriately placed in either the
study or control group. At the time of surgery (hernia repair, bariatric procedure, or
esophageal myotomy), a 30 ml venous blood sample will be drawn and stored for later testing
and analysis. The appropriate standard surgical procedure will then be performed as per
surgical attending judgment, however, during the operation, a small (approximately 1 cm2)
piece of tissue will be excised from each of 3 anatomic sites: 1) the left diaphragmatic
crus, 2) the PEL, and 3) the GHL. After removal from the abdomen, these tissue samples will
be divided into 2 pieces to be set aside for further testing at a later time.

This excised samples represent a minute amount of tissue when compared to the overall size of
the diaphragmatic crura and surrounding ligamentous attachments, and their removal is not be
expected to cause any foreseeable problem for the patient. In fact, hiatal hernia repair
often necessitates dissection of much larger crural and connective tissue pieces than this in
order to obtain complete reduction of the abdominal viscera out of the chest and subsequent
closure of the hernia defect. Following removal of these small tissue samples, the hernia
repair, esophageal myotomy, or gastric bypass/banding will then be completed in a standard
fashion.

Inclusion Criteria: Any patient undergoing paraesophageal hernia repair, esophageal myotomy,
laparoscopic gastric bypass, or laparoscopic adjustable gastric banding.

Exclusion Criteria: Pregnant females, minors, prisoners

Inclusion Criteria:

- Any patient undergoing paraesophageal hernia repair, esophageal myotomy, laparoscopic
gastric bypass, or laparoscopic adjustable gastric banding.

Exclusion Criteria:

- Pregnant females, minors, prisoners
We found this trial at
1
site
660 S Euclid Ave
Saint Louis, Missouri 63110
(314) 362-5000
Washington University School of Medicine Washington University Physicians is the clinical practice of the School...
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