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Nutritional markers in patients with diabetes and pancreatic exocrine failure

  • Laure Alexandre-Heymann
  • Amal Y. Lemoine
  • Samir Nakib
  • Nathalie Kapel
  • Séverine Ledoux
  • Etienne LargerEmail author
Original Article

Abstract

Aims

Altered pancreatic exocrine function can be observed in patients with type 1 or type 2 diabetes. In the present study, we evaluated the potential nutritional consequences of this dysfunction.

Methods

Serum concentrations of nutritional markers, including albumin, cholesterol, triacylglycerol, vitamins A, D, and E, were assessed in a cohort of 468 patients (137 with type 1 diabetes and 331 with type 2 diabetes), after exclusion of the patients with a CRP > 10 mg/l. These patients were compared with 47 patients with diseases of the exocrine pancreas and diabetes (type 3c diabetes or pancreatogenic diabetes). Fecal elastase-1 and chymotrypsin concentrations were measured and patients with type 1 and type 2 diabetes were divided into three groups according to whether zero (group NN), one (group LN), or both (group LL) concentrations were decreased.

Results

Several markers differed significantly between the groups of patients, including BMI, albumin, phosphorus, and fat-soluble vitamins. Patients with pancreatogenic diabetes had markedly more profound alterations than patients with type 1 or type 2 diabetes and altered exocrine function. However, patients with type 1 or type 2 diabetes and decreased concentrations of both elastase-1 and chymotrypsin had lower albumin, phosphorus, and vitamin A than patients with normal pancreatic exocrine function.

Conclusions

Modest nutritional alterations were found in patients with type 1 or type 2 diabetes and altered exocrine function. Patients with type 1 or type 2 diabetes and altered exocrine function may thus deserve to be screened for nutritional deficiencies.

Keywords

Diabetes Nutrition Pancreatic exocrine dysfunction Fat-soluble vitamins Fecal elastase 

Notes

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest. All investigations were performed in the context of routine patient’s care.

Ethical standard statement

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Supplementary material

592_2019_1294_MOESM1_ESM.docx (13 kb)
Supplementary material 1 (DOCX 13 KB)

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Copyright information

© Springer-Verlag Italia S.r.l., part of Springer Nature 2019

Authors and Affiliations

  1. 1.Service de DiabétologieHôpital CochinParisFrance
  2. 2.INSERM U 1016, Département Hospitalo Universitaire «AUTHORS»Université Paris DescartesParisFrance
  3. 3.Laboratoire de BiochimieHôpital CochinParisFrance
  4. 4.Laboratoire de Coprologie FonctionnelleHopital Pitié-SalpétrièreParisFrance
  5. 5.Université Paris DescartesParisFrance
  6. 6.Service des Explorations FonctionnellesHôpital Louis MourierColombesFrance
  7. 7.Université Denis DiderotParisFrance

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