Identification and validation of a multivariable prediction model based on blood plasma and serum metabolomics for the distinction of chronic pancreatitis subjects from non-pancreas disease control subjects

被引:40
作者
Adam, M. Gordian [1 ]
Beyer, Georg [2 ]
Christiansen, Nicole [3 ]
Kamlage, Beate [1 ]
Pilarsky, Christian [4 ]
Distler, Marius [5 ]
Fahlbusch, Tim [6 ]
Chromik, Ansgar [7 ]
Klein, Fritz [8 ]
Bahra, Marcus [8 ]
Uhl, Waldemar [6 ]
Gruetzmann, Robert [4 ]
Mahajan, Ujjwal M. [2 ]
Weiss, Frank U. [9 ]
Mayerle, Julia [2 ]
Lerch, Markus M. [9 ]
机构
[1] Metan Hlth GmbH, Berlin, Germany
[2] Ludwig Maximilians Univ Munchen, Dept Med 2, Munich, Bayern, Germany
[3] TrinamiX GmbH, Ludwigshafen, Rheinland Pfalz, Germany
[4] Erlangen Univ Hosp, Dept Surg, Erlangen, Bayern, Germany
[5] Dresden Univ Hosp, Clin & Outpatient Clin Visceral Thorax & Vasc Sur, Dresden, Sachsen, Germany
[6] Ruhr Univ Bochum, Dept Surg, St Josef Hosp, Bochum, Nordrhein Westf, Germany
[7] Asklepios Hosp Grp, Dept Gen & Visceral Surg, Askleipios Clin Harburg, Hamburg, Germany
[8] Charite Univ Med Berlin, Dept Surg, Campus Charite Mitte, Berlin, Germany
[9] Univ Med Greifswald, Dept Med A, Greifswald, Mecklenburg Vor, Germany
关键词
lipid metabolism; liver metabolism; pancreatic disorders; chronic pancreatitis; liver cirrhosis; HEREDITARY PANCREATITIS; CATIONIC TRYPSINOGEN; PRACTICE GUIDELINES; DEFINITION; PREVALENCE; DEFICIENCY; EXPRESSION; PROGNOSIS; DISCOVERY; DIAGNOSIS;
D O I
10.1136/gutjnl-2020-320723
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective Chronic pancreatitis (CP) is a fibroinflammatory syndrome leading to organ dysfunction, chronic pain, an increased risk for pancreatic cancer and considerable morbidity. Due to a lack of specific biomarkers, diagnosis is based on symptoms and specific but insensitive imaging features, preventing an early diagnosis and appropriate management. Design We conducted a type 3 study for multivariable prediction for individual prognosis according to the TRIPOD guidelines. A signature to distinguish CP from controls (n=160) was identified using gas chromatography-mass spectrometry and liquid chromatography-tandem mass spectrometry on ethylenediaminetetraacetic acid (EDTA)-plasma and validated in independent cohorts. Results A Naive Bayes algorithm identified eight metabolites of six ontology classes. After algorithm training and computation of optimal cut-offs, classification according to the metabolic signature detected CP with an area under the curve (AUC) of 0.85 ((95% CI 0.79 to 0.91). External validation in two independent cohorts (total n=502) resulted in similar accuracy for detection of CP compared with non-pancreatic controls in EDTA-plasma (AUC 0.85 (95% CI 0.81 to 0.89)) and serum (AUC 0.87 (95% CI 0.81 to 0.95)). Conclusions This is the first study that identifies and independently validates a metabolomic signature in plasma and serum for the diagnosis of CP in large, prospective cohorts. The results could provide the basis for the development of the first routine laboratory test for CP.
引用
收藏
页码:2150 / 2158
页数:9
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