HUGE QUESTION

heatherrose415

New member
My husband called this morning while i was gone to ask for the results.

The nurse called back and said that no genes were found, but the 7T/7T Poly T variant showed up.

I dont know what this means and neither did the nurse, the Dr. has yet to review and may not be in today.

He is pancreatic insufficient, which is what led to this test.

if any of you know, please let me know!!

Im worried sick right now.

-Heather
 

heatherrose415

New member
My husband called this morning while i was gone to ask for the results.

The nurse called back and said that no genes were found, but the 7T/7T Poly T variant showed up.

I dont know what this means and neither did the nurse, the Dr. has yet to review and may not be in today.

He is pancreatic insufficient, which is what led to this test.

if any of you know, please let me know!!

Im worried sick right now.

-Heather
 

heatherrose415

New member
My husband called this morning while i was gone to ask for the results.

The nurse called back and said that no genes were found, but the 7T/7T Poly T variant showed up.

I dont know what this means and neither did the nurse, the Dr. has yet to review and may not be in today.

He is pancreatic insufficient, which is what led to this test.

if any of you know, please let me know!!

Im worried sick right now.

-Heather
 

heatherrose415

New member
well i guess it was a huge question to me, LOL.

The nurse called back and said that dr. moss said he does not have CF. Which I would be happy to hear, but am not convinced.

His sweat tests were 41 and 30. he is pancreatic insufficient, and now, although no mutations were found, he has the 7T/7T poly T variants. which from what i read, is related to CFTR, and can cause chronic pancreatitis, and problems with the vas deferens, even with no mutations found.

will you guys please give me any insight.
Thanks!
 

heatherrose415

New member
well i guess it was a huge question to me, LOL.

The nurse called back and said that dr. moss said he does not have CF. Which I would be happy to hear, but am not convinced.

His sweat tests were 41 and 30. he is pancreatic insufficient, and now, although no mutations were found, he has the 7T/7T poly T variants. which from what i read, is related to CFTR, and can cause chronic pancreatitis, and problems with the vas deferens, even with no mutations found.

will you guys please give me any insight.
Thanks!
 

heatherrose415

New member
well i guess it was a huge question to me, LOL.

The nurse called back and said that dr. moss said he does not have CF. Which I would be happy to hear, but am not convinced.

His sweat tests were 41 and 30. he is pancreatic insufficient, and now, although no mutations were found, he has the 7T/7T poly T variants. which from what i read, is related to CFTR, and can cause chronic pancreatitis, and problems with the vas deferens, even with no mutations found.

will you guys please give me any insight.
Thanks!
 

JazzysMom

New member
Have you left a message for Steve from Ambry? He would be an excellent one to help explain things in ways that you can understand.
 

JazzysMom

New member
Have you left a message for Steve from Ambry? He would be an excellent one to help explain things in ways that you can understand.
 

JazzysMom

New member
Have you left a message for Steve from Ambry? He would be an excellent one to help explain things in ways that you can understand.
 

JazzysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>JazzysMom</b></i>

Have you left a message for Steve from Ambry? He would be an excellent one to help explain things in ways that you can understand.</end quote></div>


NEVERMIND I see you posted a message for Steve..
 

JazzysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>JazzysMom</b></i>

Have you left a message for Steve from Ambry? He would be an excellent one to help explain things in ways that you can understand.</end quote></div>


NEVERMIND I see you posted a message for Steve..
 

JazzysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>JazzysMom</b></i>

Have you left a message for Steve from Ambry? He would be an excellent one to help explain things in ways that you can understand.</end quote></div>


NEVERMIND I see you posted a message for Steve..
 

okok

New member
Hi Heather,

From what i have seen the 7t genotype is normal and and the 5t genotype is responsible for pancreatitis. I will post the following abstracts. I don't know much. I'm sure steve and your docs will know more but hopefully this will help ease your mind some.

The following abstract states that the 7t and 9t polymorphisms are normal genotypes while the 5t is assoiciated with idiopathic pancreatitis (BUT not necessarily alcholic pancreatitis).


Alcoholic pancreatitis and polymorphisms of the variable length polythymidine tract in the cystic fibrosis gene.

* Haber PS,
* Norris MD,
* Apte MV,
* Rodgers SC,
* Norton ID,
* Pirola RC,
* Roberts-Thomson IC,
* Wilson JS.

Department of Gastroenterology, Prince of Wales Hospital, Sydney, Australia.

BACKGROUND: The observation that only a minority of alcoholics develops clinical pancreatic disease has led to a search for a predisposing factor to the disease. One possible predisposing factor is mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene as cystic fibrosis leads to pancreatic injury. We have recently demonstrated that 15 common CFTR mutations are not found in patients with alcoholic pancreatitis. Another common polymorphism of the CFTR gene has recently been implicated in the pathogenesis of idiopathic chronic pancreatitis, the 5T variant of the variable length polythymidine tract in intron 8 (the normal genotypes are 7T and 9T). The 5T variant inhibits transcription of exon 9 resulting in a CFTR protein lacking chloride channel activity. The aim of this study was to determine whether the 5T variant is associated with alcoholic pancreatitis. METHODS: Fifty-two patients with alcoholic pancreatitis were identified using standardized diagnostic criteria. Fifty alcoholics without pancreatitis were also studied as controls. Genomic DNA was extracted from peripheral blood leukocytes and the polythymidine tract of intron 8 was amplified by nested polymerase chain reaction using established primers. The polymerase chain reaction products were digested with MseI, separated by electrophoresis on 15% polyacrylamide gels and genotypes assigned by comparison with known positive controls. RESULTS: The 5T allele we found in only two patients with alcoholic pancreatitis (3.9% of th index group; 95% confidence intervals 0-10%) and in seven alco holic controls. Allele frequencies for 5T, 7T, and 9T in patients with alcoholic pancreatitis were 1.9%, 85.6%, and 12.5%, respectively These did not differ from the allele frequencies in alcoholic controls (7%, 79%, and 14% for 5T, 7T, and 9T, respectively). CONCLUSION: The 5T allele was not associated with alcoholic pancreatitis. Individual susceptibility to this disease remains unexplained.


Here is another link where the most common allele in japan, the 7t, is associated with healthy people not people with pancreatitis.

Links
Polymorphism of cystic fibrosis gene in Japanese patients with chronic pancreatitis.

* Kimura S,
* Okabayashi Y,
* Inushima K,
* Yutsudo Y,
* Kasuga M.

Second Department of Internal Medicine, Kobe University School of Medicine, Japan.

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and the 5T genotype of the polythymidine tract at the exon 9 splice branch/acceptor site are shown to be associated with chronic pancreatitis in Caucasian patients. In contrast to Western countries, cystic fibrosis is extremely rare in Japan. In this study, we investigated the association of mutations or polymorphisms of the CFTR gene with chronic pancreatitis in Japanese patients. Forty-seven patients with chronic pancreatitis (alcohol-related in 31, idiopathic in 14, and familial in 2) were examined for the deltaF508 and R117H mutations and polymorphisms of intron 8. DNA was extracted from leukocytes. Mutations and polymorphisms were examined by the allele-specific polymerase chain reactions and confirmed by direct sequencing. None of the patients had deltaF508 or R117H mutations in the CFTR gene. All of 47 healthy Japanese showed the homozygous 7T/7T genotype, whereas the frequencies of 5T, 7T, and 9T alleles were 0.043, 0.894, and 0.064 in the patients, respectively. The difference in allele frequency is statistically significant. Therefore, the present study indicates the association of polymorphism of the polythymidine tract in intron 8 of the CFTR gene with chronic pancreatitis in Japanese patients.

PMID: 11117575 [PubMed - indexed for MEDLINE]
Click here to read Click here to read
 

okok

New member
Hi Heather,

From what i have seen the 7t genotype is normal and and the 5t genotype is responsible for pancreatitis. I will post the following abstracts. I don't know much. I'm sure steve and your docs will know more but hopefully this will help ease your mind some.

The following abstract states that the 7t and 9t polymorphisms are normal genotypes while the 5t is assoiciated with idiopathic pancreatitis (BUT not necessarily alcholic pancreatitis).


Alcoholic pancreatitis and polymorphisms of the variable length polythymidine tract in the cystic fibrosis gene.

* Haber PS,
* Norris MD,
* Apte MV,
* Rodgers SC,
* Norton ID,
* Pirola RC,
* Roberts-Thomson IC,
* Wilson JS.

Department of Gastroenterology, Prince of Wales Hospital, Sydney, Australia.

BACKGROUND: The observation that only a minority of alcoholics develops clinical pancreatic disease has led to a search for a predisposing factor to the disease. One possible predisposing factor is mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene as cystic fibrosis leads to pancreatic injury. We have recently demonstrated that 15 common CFTR mutations are not found in patients with alcoholic pancreatitis. Another common polymorphism of the CFTR gene has recently been implicated in the pathogenesis of idiopathic chronic pancreatitis, the 5T variant of the variable length polythymidine tract in intron 8 (the normal genotypes are 7T and 9T). The 5T variant inhibits transcription of exon 9 resulting in a CFTR protein lacking chloride channel activity. The aim of this study was to determine whether the 5T variant is associated with alcoholic pancreatitis. METHODS: Fifty-two patients with alcoholic pancreatitis were identified using standardized diagnostic criteria. Fifty alcoholics without pancreatitis were also studied as controls. Genomic DNA was extracted from peripheral blood leukocytes and the polythymidine tract of intron 8 was amplified by nested polymerase chain reaction using established primers. The polymerase chain reaction products were digested with MseI, separated by electrophoresis on 15% polyacrylamide gels and genotypes assigned by comparison with known positive controls. RESULTS: The 5T allele we found in only two patients with alcoholic pancreatitis (3.9% of th index group; 95% confidence intervals 0-10%) and in seven alco holic controls. Allele frequencies for 5T, 7T, and 9T in patients with alcoholic pancreatitis were 1.9%, 85.6%, and 12.5%, respectively These did not differ from the allele frequencies in alcoholic controls (7%, 79%, and 14% for 5T, 7T, and 9T, respectively). CONCLUSION: The 5T allele was not associated with alcoholic pancreatitis. Individual susceptibility to this disease remains unexplained.


Here is another link where the most common allele in japan, the 7t, is associated with healthy people not people with pancreatitis.

Links
Polymorphism of cystic fibrosis gene in Japanese patients with chronic pancreatitis.

* Kimura S,
* Okabayashi Y,
* Inushima K,
* Yutsudo Y,
* Kasuga M.

Second Department of Internal Medicine, Kobe University School of Medicine, Japan.

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and the 5T genotype of the polythymidine tract at the exon 9 splice branch/acceptor site are shown to be associated with chronic pancreatitis in Caucasian patients. In contrast to Western countries, cystic fibrosis is extremely rare in Japan. In this study, we investigated the association of mutations or polymorphisms of the CFTR gene with chronic pancreatitis in Japanese patients. Forty-seven patients with chronic pancreatitis (alcohol-related in 31, idiopathic in 14, and familial in 2) were examined for the deltaF508 and R117H mutations and polymorphisms of intron 8. DNA was extracted from leukocytes. Mutations and polymorphisms were examined by the allele-specific polymerase chain reactions and confirmed by direct sequencing. None of the patients had deltaF508 or R117H mutations in the CFTR gene. All of 47 healthy Japanese showed the homozygous 7T/7T genotype, whereas the frequencies of 5T, 7T, and 9T alleles were 0.043, 0.894, and 0.064 in the patients, respectively. The difference in allele frequency is statistically significant. Therefore, the present study indicates the association of polymorphism of the polythymidine tract in intron 8 of the CFTR gene with chronic pancreatitis in Japanese patients.

PMID: 11117575 [PubMed - indexed for MEDLINE]
Click here to read Click here to read
 

okok

New member
Hi Heather,

From what i have seen the 7t genotype is normal and and the 5t genotype is responsible for pancreatitis. I will post the following abstracts. I don't know much. I'm sure steve and your docs will know more but hopefully this will help ease your mind some.

The following abstract states that the 7t and 9t polymorphisms are normal genotypes while the 5t is assoiciated with idiopathic pancreatitis (BUT not necessarily alcholic pancreatitis).


Alcoholic pancreatitis and polymorphisms of the variable length polythymidine tract in the cystic fibrosis gene.

* Haber PS,
* Norris MD,
* Apte MV,
* Rodgers SC,
* Norton ID,
* Pirola RC,
* Roberts-Thomson IC,
* Wilson JS.

Department of Gastroenterology, Prince of Wales Hospital, Sydney, Australia.

BACKGROUND: The observation that only a minority of alcoholics develops clinical pancreatic disease has led to a search for a predisposing factor to the disease. One possible predisposing factor is mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene as cystic fibrosis leads to pancreatic injury. We have recently demonstrated that 15 common CFTR mutations are not found in patients with alcoholic pancreatitis. Another common polymorphism of the CFTR gene has recently been implicated in the pathogenesis of idiopathic chronic pancreatitis, the 5T variant of the variable length polythymidine tract in intron 8 (the normal genotypes are 7T and 9T). The 5T variant inhibits transcription of exon 9 resulting in a CFTR protein lacking chloride channel activity. The aim of this study was to determine whether the 5T variant is associated with alcoholic pancreatitis. METHODS: Fifty-two patients with alcoholic pancreatitis were identified using standardized diagnostic criteria. Fifty alcoholics without pancreatitis were also studied as controls. Genomic DNA was extracted from peripheral blood leukocytes and the polythymidine tract of intron 8 was amplified by nested polymerase chain reaction using established primers. The polymerase chain reaction products were digested with MseI, separated by electrophoresis on 15% polyacrylamide gels and genotypes assigned by comparison with known positive controls. RESULTS: The 5T allele we found in only two patients with alcoholic pancreatitis (3.9% of th index group; 95% confidence intervals 0-10%) and in seven alco holic controls. Allele frequencies for 5T, 7T, and 9T in patients with alcoholic pancreatitis were 1.9%, 85.6%, and 12.5%, respectively These did not differ from the allele frequencies in alcoholic controls (7%, 79%, and 14% for 5T, 7T, and 9T, respectively). CONCLUSION: The 5T allele was not associated with alcoholic pancreatitis. Individual susceptibility to this disease remains unexplained.


Here is another link where the most common allele in japan, the 7t, is associated with healthy people not people with pancreatitis.

Links
Polymorphism of cystic fibrosis gene in Japanese patients with chronic pancreatitis.

* Kimura S,
* Okabayashi Y,
* Inushima K,
* Yutsudo Y,
* Kasuga M.

Second Department of Internal Medicine, Kobe University School of Medicine, Japan.

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and the 5T genotype of the polythymidine tract at the exon 9 splice branch/acceptor site are shown to be associated with chronic pancreatitis in Caucasian patients. In contrast to Western countries, cystic fibrosis is extremely rare in Japan. In this study, we investigated the association of mutations or polymorphisms of the CFTR gene with chronic pancreatitis in Japanese patients. Forty-seven patients with chronic pancreatitis (alcohol-related in 31, idiopathic in 14, and familial in 2) were examined for the deltaF508 and R117H mutations and polymorphisms of intron 8. DNA was extracted from leukocytes. Mutations and polymorphisms were examined by the allele-specific polymerase chain reactions and confirmed by direct sequencing. None of the patients had deltaF508 or R117H mutations in the CFTR gene. All of 47 healthy Japanese showed the homozygous 7T/7T genotype, whereas the frequencies of 5T, 7T, and 9T alleles were 0.043, 0.894, and 0.064 in the patients, respectively. The difference in allele frequency is statistically significant. Therefore, the present study indicates the association of polymorphism of the polythymidine tract in intron 8 of the CFTR gene with chronic pancreatitis in Japanese patients.

PMID: 11117575 [PubMed - indexed for MEDLINE]
Click here to read Click here to read
 

okok

New member
Hi again heather,

I just want to explain a little better. An allele is a word used to refer to different versions of a gene. Some versions of genes can have disease causing mutations such as the Df508 version of the CFTR gene other versions of genes can have non disease causing mutations and they are typically referred to as polymorphisms since they are normal genetic variations.

The poly t track is a part of the CFTR gene which repeats the same base (T) over and over. The number 5 or 7 or 9 refers to the number of repeats. From what i have read the non-disease causing or normal versions of the poly T track are the 7t and 9t versions. It makes sense that either too few repeated t's (as in the case of the 5t allele) or too many repeated t's (perhaps greater than 9 repeats) could cause problems in the protien's structure and possibly lead to disease.

your child's gentype is 7t/7t which means that both chromosomes carry the 7t allele of the poly t track.

Still it is possible that your child has other unknown mutations of the CFTR. Hopefully not though! You will have to discuss all of this with your docs/genetic counselor but i'm guessing that you will just have to follow your child's symptoms. If i remember correctly at this time your child is just def for amylase right?? If your child has CF and that is what is responsible for the amylase def then most likely over time other enzymes will probably go too. I think you have seen a pulmo at stanford too right??? i hope they can help sort this all out. I think it is good news though that ambry found no mutations and the normal 7t varient.

good luck and let us know how you are doing with all this!
 

okok

New member
Hi again heather,

I just want to explain a little better. An allele is a word used to refer to different versions of a gene. Some versions of genes can have disease causing mutations such as the Df508 version of the CFTR gene other versions of genes can have non disease causing mutations and they are typically referred to as polymorphisms since they are normal genetic variations.

The poly t track is a part of the CFTR gene which repeats the same base (T) over and over. The number 5 or 7 or 9 refers to the number of repeats. From what i have read the non-disease causing or normal versions of the poly T track are the 7t and 9t versions. It makes sense that either too few repeated t's (as in the case of the 5t allele) or too many repeated t's (perhaps greater than 9 repeats) could cause problems in the protien's structure and possibly lead to disease.

your child's gentype is 7t/7t which means that both chromosomes carry the 7t allele of the poly t track.

Still it is possible that your child has other unknown mutations of the CFTR. Hopefully not though! You will have to discuss all of this with your docs/genetic counselor but i'm guessing that you will just have to follow your child's symptoms. If i remember correctly at this time your child is just def for amylase right?? If your child has CF and that is what is responsible for the amylase def then most likely over time other enzymes will probably go too. I think you have seen a pulmo at stanford too right??? i hope they can help sort this all out. I think it is good news though that ambry found no mutations and the normal 7t varient.

good luck and let us know how you are doing with all this!
 

okok

New member
Hi again heather,

I just want to explain a little better. An allele is a word used to refer to different versions of a gene. Some versions of genes can have disease causing mutations such as the Df508 version of the CFTR gene other versions of genes can have non disease causing mutations and they are typically referred to as polymorphisms since they are normal genetic variations.

The poly t track is a part of the CFTR gene which repeats the same base (T) over and over. The number 5 or 7 or 9 refers to the number of repeats. From what i have read the non-disease causing or normal versions of the poly T track are the 7t and 9t versions. It makes sense that either too few repeated t's (as in the case of the 5t allele) or too many repeated t's (perhaps greater than 9 repeats) could cause problems in the protien's structure and possibly lead to disease.

your child's gentype is 7t/7t which means that both chromosomes carry the 7t allele of the poly t track.

Still it is possible that your child has other unknown mutations of the CFTR. Hopefully not though! You will have to discuss all of this with your docs/genetic counselor but i'm guessing that you will just have to follow your child's symptoms. If i remember correctly at this time your child is just def for amylase right?? If your child has CF and that is what is responsible for the amylase def then most likely over time other enzymes will probably go too. I think you have seen a pulmo at stanford too right??? i hope they can help sort this all out. I think it is good news though that ambry found no mutations and the normal 7t varient.

good luck and let us know how you are doing with all this!
 

okok

New member
I found another relevant abstract stating that the 5t allele not 7t is associated with idiopathic pancreatitis.

PS I'm not positive about this but from what i have read it sounds like the issues related to the 5T allele are not completely penetrant OR in other words just having the 5t allele does not mean it will cause an individual problems. Apparently having the 5t allele and 12 TG repeats increases the chances that the 5t allele will cause problems.

here us that abstract:

Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controls.

* Weiss FU,
* Simon P,
* Bogdanova N,
* Mayerle J,
* Dworniczak B,
* Horst J,
* Lerch MM.

Department of Gastroenterology, Endocrinology and Nutrition, Ernst-Moritz-Arndt-Universitat Greifswald, Germany.

BACKGROUND: Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene-many of which cause cystic fibrosis-have also been reported in patients with chronic pancreatitis. The authors examine whether mild or severe CFTR mutations, homozygous or compound heterozygous CFTR mutations, or even simple cystic fibrosis carrier status alone increases the risk of developing pancreatitis. METHODS: After exclusion of patients with trypsinogen (PRSS1) mutations, cystic fibrosis, or pulmonary disease, and with known risk factors for pancreatitis 67 patients with idiopathic chronic pancreatitis (ICP) from northwest Germany and 60 geographically and ethnically matched controls were recruited. The entire coding region of the CFTR gene was sequenced in all patients and controls. ICP patients were also analysed for serine protease inhibitor Kazal type 1 (SPINK1) gene mutations. RESULTS: Abnormal CFTR alleles were found to be twice as frequent in ICP patients as in controls (25/134 v 11/120; p<0.05). Three of four severe CFTR mutations detected in patients were compound heterozygous with another abnormal CFTR allele, whereas among controls three severe CFTR mutations were found in heterozygous cystic fibrosis carriers. In ICP patients 19 uncommon/mild mutations, including combinations of the 5T allele with 12TG repeats, were identified compared with only five in controls (p = 0.012). Heterozygous SPINK1 mutations were detected in eight ICP patients (15% v 1% in controls) but only one also carried an additional mild CFTR mutation. CONCLUSIONS: These data show that not only compound heterozygosity, but also cystic fibrosis carrier status for different types of CFTR mutations, including uncommon/mild mutations, significantly increase the risk of developing pancreatitis. Although 45% of the study's ICP patients carried predisposing genetic risk factors (for example, mutations in CFTR or SPINK1), the authors found no evidence that the risk conveyed by CFTR mutations depends on co-inherited SPINK1 mutations.
 

okok

New member
I found another relevant abstract stating that the 5t allele not 7t is associated with idiopathic pancreatitis.

PS I'm not positive about this but from what i have read it sounds like the issues related to the 5T allele are not completely penetrant OR in other words just having the 5t allele does not mean it will cause an individual problems. Apparently having the 5t allele and 12 TG repeats increases the chances that the 5t allele will cause problems.

here us that abstract:

Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controls.

* Weiss FU,
* Simon P,
* Bogdanova N,
* Mayerle J,
* Dworniczak B,
* Horst J,
* Lerch MM.

Department of Gastroenterology, Endocrinology and Nutrition, Ernst-Moritz-Arndt-Universitat Greifswald, Germany.

BACKGROUND: Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene-many of which cause cystic fibrosis-have also been reported in patients with chronic pancreatitis. The authors examine whether mild or severe CFTR mutations, homozygous or compound heterozygous CFTR mutations, or even simple cystic fibrosis carrier status alone increases the risk of developing pancreatitis. METHODS: After exclusion of patients with trypsinogen (PRSS1) mutations, cystic fibrosis, or pulmonary disease, and with known risk factors for pancreatitis 67 patients with idiopathic chronic pancreatitis (ICP) from northwest Germany and 60 geographically and ethnically matched controls were recruited. The entire coding region of the CFTR gene was sequenced in all patients and controls. ICP patients were also analysed for serine protease inhibitor Kazal type 1 (SPINK1) gene mutations. RESULTS: Abnormal CFTR alleles were found to be twice as frequent in ICP patients as in controls (25/134 v 11/120; p<0.05). Three of four severe CFTR mutations detected in patients were compound heterozygous with another abnormal CFTR allele, whereas among controls three severe CFTR mutations were found in heterozygous cystic fibrosis carriers. In ICP patients 19 uncommon/mild mutations, including combinations of the 5T allele with 12TG repeats, were identified compared with only five in controls (p = 0.012). Heterozygous SPINK1 mutations were detected in eight ICP patients (15% v 1% in controls) but only one also carried an additional mild CFTR mutation. CONCLUSIONS: These data show that not only compound heterozygosity, but also cystic fibrosis carrier status for different types of CFTR mutations, including uncommon/mild mutations, significantly increase the risk of developing pancreatitis. Although 45% of the study's ICP patients carried predisposing genetic risk factors (for example, mutations in CFTR or SPINK1), the authors found no evidence that the risk conveyed by CFTR mutations depends on co-inherited SPINK1 mutations.
 
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