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==Historical Perspective==
==Historical Perspective==
{{Family tree/start}}
{{Family tree | | | | | | C01 |-| C02 |-| C03 | |C01= '''Beginning of the mankind'''|C02= '''''2.5 million years ago'''''|C03= Hunting and eating meat, fruits, seeds, and nuts}}
{{Family tree | | | | | | |:| | | | | | | | | | | }}
{{Family tree | | | | | | |:| | | | | | | | | | | }}
{{Family tree | | | | | | |:| | | | | | | | | | | }}
{{Family tree | | | | | | |:| | | | | | | | | | | }}
{{Family tree | | | | | | G01 |-| G02 |-| G03 | |G01= '''10,000 years ago'''|G02= '''''Neolithic period'''''|G03= Discovery of agriculture. <br>New [[antigens]] have been introduced to human diet<br> (protein from cow, goat, and donkey milk, bird eggs, and various cereals).<br> First cases of celiac disease. }}
{{Family tree | | | | | | |:| | | | | | | | | | | }}
{{Family tree | | A01 |-| B01 |-| B02 |-| B03 | |A01= '''Discovery'''|B01= '''2,000 years ago'''|B02= '''''Aretaeus'''''<br>A Cappadocian physician|B03=Described celiac disease, calling it '''''koiliakos'''''.<br> It came from Greek word ''''''koelia''''' ([[abdomen]]), representing a "suffering abdomen"}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | C01 |-| C02 |-| C03 | |C01= '''1812'''|C02= '''''Mathew Baillie'''''<br>A Scottish physician|C03=Described some adult patients experiencing [[malnutrition]] and [[bloating]] along with [[chronic diarrhea]] }}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | G01 |-| G02 |-| G03 | |G01= '''1887'''|G02= '''''Samuel Gee'''''<br>A famous English [[pediatrician]]|G03= Gave a detailed explanation of celiac disease, presenting a lecture on "Celiac affection"}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | E01 |-| E02 |-| E03 | |E01= '''1924'''|E02= '''''Sidney Haas'''''<br>A New York city [[pediatrician]]|E03= Used a new [[Dietetics|dietetic]] therapeutic option for 10 children with celiac disease, '''''the banana diet'''''}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | G01 |-| G02 |-| G03 | |G01= '''1949'''|G02= '''''Wood'''''<br>An Australian [[gastroenterologist]]|G03= Invented a simple flexible biopsy tube which could be used for GI biopsies without requiring [[X-ray]] or [[gastroscope]] assistance}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | D01 |-| D02 |-| D03 | |D01= '''1950'''|D02= '''''Wim Dicke'''''<br>A Dutch [[pediatrician]]|D03= Suggested in his doctoral thesis that elimination of [[wheat]], rye, and [[Oat|oats]] from diet would result in cure of celiac disease}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | G01 |-| G02 |-| G03 | |G01= '''1950'''|G02= ''''' Wim Dicke's colleagues,<br> Weijers and Van de Kamer'''''|G03= Presented [[stool]] [[fat]] measurement as a method to diagnose celiac disease}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | F01 |-| F02 |-| F03 | |F01= '''1954'''|F02= ''''' John Paulley'''''<br>An English [[pathologist]] from Ipswich |F03= Discovered the [[pathophysiology]] of celiac disease, that is [[histological]] abnormalities in [[small intestine]] lining}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | A01 |-| G01 |-| G02 |-| G03 | |A01='''Diagnosis'''|G01= '''1955'''|G02= ''''' Marcelo Royer'''''<br>An Argentinian [[gastroenterologist]] from Buenos Aires|G03= Developed a technique for [[duodenal]] [[biopsy]] under [[fluoroscopic]] vision}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | G01 |-| G02 |-| G03 | |G01='''1956'''|G02= ''''' Margot Shiner'''''<br>A German-British [[gastroenterologist]]|G03= Developed another technique for [[duodenal]] [[biopsy]] under [[fluoroscopic]] vision}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | G01 |-| G02 |-| G03 | |G01='''1964'''|G02= ''''' Berger'''''<br>A Switzerland [[immunologist]]|G03= Detected and reported anti [[gliadin]] [[antibodies]] in children with celiac disease}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | G01 |-| G02 |-| G03 | |G01='''1969'''|G02= ''''' European Society of Pediatric Gastroenterology<br> (now ESPGHAN)'''''|G03= Gave the diagnostic tool of “'''''Interlaken criteria'''''”, which was used for about 20 years}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | G01 |-| G02 |-| G03 | |G01='''1971'''|G02= ''''' Seah'''''<br>A British physician|G03= Discovered an [[Autoantibody|auto-antibody]], the anti-reticulin; showing that [[antibody]] is not necessarily an anti-food [[protein]]}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree | | | | | | G01 |-| G02 |-| G03 | |G01='''1983'''|G02= ''''' Chorzelski'''''<br>A Polish [[dermatologist]] from Warsaw|G03= Discovered anti-[[endomysium]] [[antibodies]] and [[dermatitis herpetiformis]] in celiac disease patients}}
{{Family tree | | | | | | |!| | | | | | | | | | | }}
{{Family tree |boxstyle=text-align: center; | | S01 |-| S02 |-| S03 |-| S04 | |S01='''Treatment'''|S02= '''Recently'''|S03= ''''' Main guidelines'''''|S04= • [[Agency for Healthcare Research and Quality]] (AHRQ, 2004)<ref name="urlCeliac Disease: Summary - AHRQ Evidence Report Summaries - NCBI Bookshelf">{{cite web |url=https://www.ncbi.nlm.nih.gov/books/NBK11885/ |title=Celiac Disease: Summary - AHRQ Evidence Report Summaries - NCBI Bookshelf |format= |work= |accessdate=}}</ref><br>• [[American Gastroenterological Association]] (AGA, 2006)<ref name="pmid17087937">{{cite journal |vauthors=Rostom A, Murray JA, Kagnoff MF |title=American Gastroenterological Association (AGA) Institute technical review on the diagnosis and management of celiac disease |journal=Gastroenterology |volume=131 |issue=6 |pages


==Pathophysiology==
==Pathophysiology==

Revision as of 23:22, 20 April 2024

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Imam Ali Shah, MBBS [2]

Synonyms and keywords: Idiopathic Cirrhosis

Overview

Cryptogenic cirrhosis (CC) is defined as cirrhosis of unknown origin. It is a diagnosis of exclusion and is only made after extensive investigative workup when the underlying cause of cirrhosis remains elusive. The cause of this condition is, by definition, unknown; however, there are correlations suggesting that metabolic dysfunction-associated steatohepatitis (MASH) plays a significant role . Advances in investigative methods, understanding of liver disease, and acknowledgment of metabolic dysfunction-associated steatohepatitis (MASH) as a plausible cause have led to a significant decrease in the use of this term.

Historical Perspective

{{Family tree |boxstyle=text-align: center; | | S01 |-| S02 |-| S03 |-| S04 | |S01=Treatment|S02= Recently|S03= Main guidelines|S04= • Agency for Healthcare Research and Quality (AHRQ, 2004)[1]
American Gastroenterological Association (AGA, 2006) [2] Genome-wide association studies have uncovered loss-of-function genetic variants that offer protection against liver diseases including CC. Of note is the loss-of-function mutation in one copy of the CIDEB gene, which was identified in a large exome sequencing study to be associated with a lower risk of cirrhosis from any cause.[3]

Associated Conditions

Cryptogenic cirrhosis has a strong association with metabolic disorders, including hypertension, dyslipidemia, diabetes, and hyperuricemia. However metabolic-dysfunction associated steatohepatitis must be ruled out to diagnose the condition.

Gross and Microscopic Pathology

CC has a similar histopathological findings to non-cryptogenic cirrhosis and is characterized by nodular liver morphology due to fibrous septa formation, dividing the liver into regenerative hepatocyte nodules microscopically. Fibrosis is prominent, disrupting the liver's architecture, with associated hepatocellular changes such as atrophy, hypertrophy, and fatty infiltration. Inflammation and necrosis may be evident, along with features like Mallory-Denk bodies, megamitochondria, and iron deposition, reflecting the chronic liver injury and regenerative processes ongoing within the liver.

Causes

Although the exact cause of cryptogenic cirrhosis remains uncertain, accumulating evidence and research increasingly suggest that metabolic dysfunction-associated steatotic liver disease (MASLD) may be the underlying factor.[4] Several studies have demonstrated the underlying role of genetic factors in occurrence and progression of CC.[5] [6]

Differentiating Cryptogenic Cirrhosis from other Diseases

While there's limited data explicitly differentiating the characteristics of cryptogenic cirrhosis from non-cryptogenic cirrhosis,studies have highlighted the following discernible differences between the two regarding the associations and complications of cirrhosis:

Metabolic Syndrome: Cryptogenic cirrhosis is significantly more prevalent in individuals with underlying metabolic derangements, including hypertension, dyslipidemia, diabetes, and coronary artery disease.

Cardiovascular disease: CC is associated with a higher incidence of cardiovascular disease.

Cancer: Studies have shown higher and earlier occurrence of hepatocellular carcinoma (HCC) and extrahepatic cancer in cryptogenic cirrhosis.[7] HCC also frequently presents at an advanced stage in patients with cryptogenic cirrhosis, likely due to insufficient surveillance measures. Consequently, treatment options are constrained, resulting in shorter survival periods.[8]

Epidemiology and Demographics

Age

Studies indicate that cryptogenic cirrhosis tends to occur more frequently in older individuals compared to non-cryptogenic cirrhosis, with some research suggesting an age difference of approximately ten years [9]. Additionally, it is more prevalent among individuals who have obesity, diabetes, and other metabolic comorbidities.

Gender

Cryptogenic cirrhosis is more common in females, which can partly be explained by higher prevalence of alcoholic liver disease in men globally.[10]

Race

No ethnic predilection has been observed in cryptogenic cirrhosis.

Developed vs. Developing Countries

Cryptogenic cirrhosis is a more frequent diagnosis in resource-limited and developing economies, probably due to lower availability of more advanced diagnostic modalities.

Risk Factors

Screening

Natural History, Complications and Prognosis

Cryptogenic cirrhosis is an irreversible chronic liver disease characterized by chronic liver injury, inflammation, fibrosis, and distortion and nodularity of liver architecture. The natural history of CC characterized by an asymptomatic phase, known as "compensated cirrhosis," followed by a progressive phase known as "decompensated cirrhosis". Decompensated cirrhosis is end-stage liver disease (ESLD) and is marked by the development of complications of portal hypertension and/or liver dysfunction, similar to non-cryptogenic cirrhosis.

Complications

Patients with cryptogenic cirrhosis are at risk of developing complications associated with advanced liver disease. These include portal hypertension and associated complications, hepatic encephalopathy, spontaneous bacterial peritonitis, hepatorenal syndrome, hepatocellular carcinoma, and death.

Prognosis

The prognosis of cryptogenic cirrhosis depends on various factors including the stage of cirrhosis at diagnosis, the presence of complications, and the response to treatment. Early diagnosis and intervention may improve outcomes, but cryptogenic cirrhosis can still carry a significant risk of morbidity and mortality.

Diagnosis

Diagnostic Criteria

There are no standardized diagnostic criteria for CC and it is best defined by exclusion.

History

A directed history should be obtained to ascertain

Symptoms

"Type symptom here" is pathognomonic of the "type disease name here".

"Type non specific symptoms" may be present.

Past Medical History

Diagnosing CC requires a rigorous past medical history evaluations and the presence of any metabolic disorder needs to be ruled to diagnose the condition.

Family History

Physical Examination

Appearance of the Patient

Vital Signs

Skin

Head

Eyes

Ear

Nose

Mouth

Throat

Heart

Lungs

Abdomen

Extremities

Neurologic

Genitals

Other

Laboratory Findings

Electrolyte and Biomarker Studies

Electrocardiogram

Chest X Ray

CT

MRI

Echocardiography or Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Pharmacotherapy

Acute Pharmacotherapies

Chronic Pharmacotherapies

Surgery and Device Based Therapy

Indications for Surgery

Pre-Operative Assessment

Post-Operative Management

Transplantation

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

References

  1. "Celiac Disease: Summary - AHRQ Evidence Report Summaries - NCBI Bookshelf".
  2. Mercado-Irizarry A, Torres EA (2016). "Cryptogenic cirrhosis: Current knowledge and future directions". Clin Liver Dis (Hoboken). 7 (4): 69–72. doi:10.1002/cld.539. PMC 6490261. PMID 31041033.
  3. Verweij N, Haas ME, Nielsen JB, Sosina OA, Kim M, Akbari P; et al. (2022). "Germline Mutations in CIDEB and Protection against Liver Disease". N Engl J Med. 387 (4): 332–344. doi:10.1056/NEJMoa2117872. PMID 35939579 Check |pmid= value (help).
  4. Verweij N, Haas ME, Nielsen JB, Sosina OA, Kim M, Akbari P; et al. (2022). "Germline Mutations in CIDEB and Protection against Liver Disease". N Engl J Med. 387 (4): 332–344. doi:10.1056/NEJMoa2117872. PMID 35939579 Check |pmid= value (help).
  5. Giannini EG, Marabotto E, Savarino V, Trevisani F, di Nolfo MA, Del Poggio P; et al. (2009). "Hepatocellular carcinoma in patients with cryptogenic cirrhosis". Clin Gastroenterol Hepatol. 7 (5): 580–5. doi:10.1016/j.cgh.2009.01.001. PMID 19418607.
  6. Perumpail RB, Liu A, Wong RJ, Ahmed A, Harrison SA (2015). "Pathogenesis of hepatocarcinogenesis in non-cirrhotic nonalcoholic fatty liver disease: Potential mechanistic pathways". World J Hepatol. 7 (22): 2384–8. doi:10.4254/wjh.v7.i22.2384. PMC 4598608. PMID 26464753.
  7. Rinaldi L, Nascimbeni F, Giordano M, Masetti C, Guerrera B, Amelia A; et al. (2017). "Clinical features and natural history of cryptogenic cirrhosis compared to hepatitis C virus-related cirrhosis". World J Gastroenterol. 23 (8): 1458–1468. doi:10.3748/wjg.v23.i8.1458. PMC 5330831. PMID 28293093.
  8. Giannini EG, Marabotto E, Savarino V, Trevisani F, di Nolfo MA, Del Poggio P; et al. (2009). "Hepatocellular carcinoma in patients with cryptogenic cirrhosis". Clin Gastroenterol Hepatol. 7 (5): 580–5. doi:10.1016/j.cgh.2009.01.001. PMID 19418607.
  9. Caldwell SH, Oelsner DH, Iezzoni JC, Hespenheide EE, Battle EH, Driscoll CJ (1999). "Cryptogenic cirrhosis: clinical characterization and risk factors for underlying disease". Hepatology. 29 (3): 664–9. doi:10.1002/hep.510290347. PMID 10051466.
  10. Caldwell SH, Oelsner DH, Iezzoni JC, Hespenheide EE, Battle EH, Driscoll CJ (1999). "Cryptogenic cirrhosis: clinical characterization and risk factors for underlying disease". Hepatology. 29 (3): 664–9. doi:10.1002/hep.510290347. PMID 10051466.
 
 
 
 
 
Beginning of the mankind
 
2.5 million years ago
 
Hunting and eating meat, fruits, seeds, and nuts
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
10,000 years ago
 
Neolithic period
 
Discovery of agriculture.
New antigens have been introduced to human diet
(protein from cow, goat, and donkey milk, bird eggs, and various cereals).
First cases of celiac disease.
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Discovery
 
2,000 years ago
 
Aretaeus
A Cappadocian physician
 
Described celiac disease, calling it koiliakos.
It came from Greek word 'koelia (abdomen), representing a "suffering abdomen"
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1812
 
Mathew Baillie
A Scottish physician
 
Described some adult patients experiencing malnutrition and bloating along with chronic diarrhea
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1887
 
Samuel Gee
A famous English pediatrician
 
Gave a detailed explanation of celiac disease, presenting a lecture on "Celiac affection"
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1924
 
Sidney Haas
A New York city pediatrician
 
Used a new dietetic therapeutic option for 10 children with celiac disease, the banana diet
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1949
 
Wood
An Australian gastroenterologist
 
Invented a simple flexible biopsy tube which could be used for GI biopsies without requiring X-ray or gastroscope assistance
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1950
 
Wim Dicke
A Dutch pediatrician
 
Suggested in his doctoral thesis that elimination of wheat, rye, and oats from diet would result in cure of celiac disease
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1950
 
Wim Dicke's colleagues,
Weijers and Van de Kamer
 
Presented stool fat measurement as a method to diagnose celiac disease
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1954
 
John Paulley
An English pathologist from Ipswich 
 
Discovered the pathophysiology of celiac disease, that is histological abnormalities in small intestine lining
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Diagnosis
 
1955
 
Marcelo Royer
An Argentinian gastroenterologist from Buenos Aires
 
Developed a technique for duodenal biopsy under fluoroscopic vision
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1956
 
Margot Shiner
A German-British gastroenterologist
 
Developed another technique for duodenal biopsy under fluoroscopic vision
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1964
 
Berger
A Switzerland immunologist
 
Detected and reported anti gliadin antibodies in children with celiac disease
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1969
 
European Society of Pediatric Gastroenterology
(now ESPGHAN)
 
Gave the diagnostic tool of “Interlaken criteria”, which was used for about 20 years
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1971
 
Seah
A British physician
 
Discovered an auto-antibody, the anti-reticulin; showing that antibody is not necessarily an anti-food protein
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1983
 
Chorzelski
A Polish dermatologist from Warsaw
 
Discovered anti-endomysium antibodies and dermatitis herpetiformis in celiac disease patients