Screening for undiagnosed pancreatic exocrine insufficiency (PEI) in a cohort of diabetic patients using faecal elastase testing and PEI scoring system

被引:1
|
作者
Parihar, V. [1 ,6 ]
Ballester, R. [1 ]
Ridgway, P. F. [3 ,4 ]
Conlon, K. C. [3 ,4 ]
Gibney, J. [5 ]
Ryan, B. M. [1 ,2 ]
机构
[1] Tallaght Univ Hosp, Dept Gastroenterol, Dublin, Ireland
[2] Trinity Coll Dublin, Dept Clin Med, Dublin, Ireland
[3] Tallaght Univ Hosp, Dept Surg, Dublin, Ireland
[4] Trinity Coll Dublin, Dublin, Ireland
[5] Tallaght Univ Hosp, Dept Endocrinol, Dublin, Ireland
[6] Letterkenny Univ Hosp, Dept Gastroenterol, Letterkenny, Ireland
关键词
Diabetes; Pancreatic exocrine insufficiency; Faecal elastase (FE1); Pancreatic exocrine insufficiency score (PEI-S); MELLITUS; DIAGNOSIS; MARKER; TYPE-1;
D O I
10.1007/s00592-024-02307-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Type 1 and type 2 diabetes mellitus (DM) are often accompanied by mild forms of pancreatic exocrine insufficiency (PEI). The prevalence rates of PEI in diabetic patients are unclear and variable depending on the testing modality and the studies published. The clinical consequences of PEI in diabetics are also not well defined. Aim We aimed to determine the prevalence of PEI in a diabetic cohort using the faecal elastase-1 (FE-1) assay as a screening test and to validate a patient-reported symptom-based scoring system, the (PEI-S) for diagnosing PEI within this patient population. Methods Two hundred and three diabetic patients attending diabetic and gastroenterology outpatients of a university hospital without previously known PEI were recruited for the study. Demographic parameters, PEI score (PEI-S), and glycated hemoglobin (HBA1c) were documented in standardized data sheets, and a stool sample was obtained. A FE-1 value < 200 mu g/g and or a PEIS of > 0.6 was used as the screening cut-off for PEI. Results One hundred sixty-six patients returned faecal samples. The prevalence of PEI, as measured by low FE-1, was 12%. Smoking was associated with an increased risk of developing PEI in this diabetic population. No other independent risk factors were identified. The PEI-S system did not differentiate between people with diabetes having a normal and low FE1. Conclusion 12% of this mixed, real-life cohort of type 1 and 2 DM patients had undiagnosed PEI, as defined by an FE-1 score of less than 200 mu g/g. While this may appear low, given the rising prevalence of type 2 DM worldwide, there is likely an unrecognized burden of PEI, which has long-term health consequences for those affected. The PEI-S, a symptom-scoring system for patients with PEI, did not perform well in this patient group.
引用
收藏
页码:1301 / 1307
页数:7
相关论文
共 10 条
  • [1] Applicability of the Pancreatic Exocrine Insufficiency Test (PEI-TEST) in Pediatric Patients
    Guven, Burcu
    Ozkaya, Esra
    Karakullukcu, Serdar
    Imamoglu, Mustafa Selcuk
    Cakir, Murat
    CLINICAL PEDIATRICS, 2025, 64 (01) : 118 - 124
  • [2] Performance of faecal elastase 1 test against the "gold standard" 3 day faecal fat collection test for the diagnosis of pancreatic exocrine insufficiency (PEI) in patients with chronic pancreatitis: it is time to change to cutoff value!
    Nam Nguyen
    Safaeian, Romina
    Zobel, Joshua
    Lebreton, Luc
    Smith, Gary
    Jais, Philippe
    Schue, Mathieu
    Spoor, Thijs
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2019, 34 : 807 - 807
  • [3] Faecal elastase testing and factors linked with development of pancreatic exocrine insufficiency in diabetes: the Belfast Trust experience
    Johnston, Philip C.
    Thompson, Judith
    Roberts, Brona
    McKee, Allison
    Taylor, Mark
    Ellison, Victoria
    PRACTICAL DIABETES, 2022, 39 (04) : 38 - 41
  • [4] The prevalence of small intestinal bacterial overgrowth in non-surgical patients with chronic pancreatitis and pancreatic exocrine insufficiency (PEI)
    Chonchubhair, Hazel M. Ni
    Bashir, Yasir
    Dobson, Mark
    Ryan, Barbara M.
    Duggan, Sinead N.
    Conlon, Kevin C.
    PANCREATOLOGY, 2018, 18 (04) : 379 - 385
  • [5] Potential for Screening for Pancreatic Exocrine Insufficiency Using the Fecal Elastase-1 Test
    J. Enrique Domínguez-Muñoz
    Philip D. Hardt
    Markus M. Lerch
    Matthias J. Löhr
    Digestive Diseases and Sciences, 2017, 62 : 1119 - 1130
  • [6] Potential for Screening for Pancreatic Exocrine Insufficiency Using the Fecal Elastase-1 Test
    Enrique Dominguez-Munoz, J.
    Hardt, Philip D.
    Lerch, Markus M.
    Lohr, Matthias J.
    DIGESTIVE DISEASES AND SCIENCES, 2017, 62 (05) : 1119 - 1130
  • [7] Are we missing pancreatic exocrine insufficiency in 'at-risk' groups? Prospective assessment of the current practice and yield of faecal elastase testing in patients with diabetes mellitus, HIV and/or high alcohol intake
    Jalal, Mustafa
    Leeds, John S.
    Ching, Hey-Long
    Oprescu, Andrei
    Tunbridge, Ann
    Greig, Julia
    Tesfaye, Solomon
    Hopper, Andrew D.
    CLINICAL MEDICINE, 2023, 23 (06) : 588 - 593
  • [8] Exocrine Pancreatic Insufficiency, as Assessed by Fecal Elastase-1 Levels, in Diabetic Patients: An Estimate of Prevalence in Prospective Studies
    Andriulli, Angelo
    Ippolito, Antonio Massimo
    Festa, Virginia
    Valvano, Maria Rosa
    Merla, Antonio
    Bossa, Fabrizio
    Niro, Grazia
    Napolitano, Grazia
    Benini, Luigi
    Vantini, Italo
    JOURNAL OF DIABETES & METABOLISM, 2014, 5 (06)
  • [9] High prevalence of steatorrhea in 101 diabetic patients likely to suffer from exocrine pancreatic insufficiency according to low fecal elastase 1 concentrations - A prospective multicenter study
    Hardt, PD
    Hauenschild, A
    Jaeger, C
    Teichmann, J
    Bretzel, RG
    Kloer, HU
    DIGESTIVE DISEASES AND SCIENCES, 2003, 48 (09) : 1688 - 1692
  • [10] High prevalence of steatorrhea in 101 diabetic patients likely to suffer from exocrine pancreatic insufficiency according to low fecal elastase 1 concentrations a prospective multicenter study
    Philip D. Hardt
    Annette Hauenschild
    Clemens Jaeger
    Joachim Teichmann
    Reinhard G. Bretzel
    Hans U. Kloer
    Digestive Diseases and Sciences, 2003, 48 (9) : 1688 - 1692