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Erschienen in: Pediatric Nephrology 4/2018

07.12.2017 | Original Article

D-lactic acidosis in humans: systematic literature review

verfasst von: Davide G. A. M. Bianchetti, Giacomo S. Amelio, Sebastiano A. G. Lava, Mario G. Bianchetti, Giacomo D. Simonetti, Carlo Agostoni, Emilio F. Fossali, Gregorio P. Milani

Erschienen in: Pediatric Nephrology | Ausgabe 4/2018

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Abstract

Background

D-lactic acidosis is an uncommon and challenging form of metabolic acidosis that may develop in short bowel syndrome. It has been documented exclusively in case reports and small case series.

Methods

We performed a review of the literature in the National Library of Medicine and Excerpta Medica databases.

Results

We identified 84 original reports published between 1977 and 2017. D-lactic acidosis was observed in 98 individuals ranging in age from 7 months to 86 years with short bowel syndrome. The clinical presentation included Kussmaul breathing, confusion, slurred speech, and gait disturbances. Furthermore, among 99 consecutive patients with short bowel syndrome, 21 reported having episodes with symptoms consistent with D-lactic acidosis. In addition, D-lactic acid might also contribute to acidosis in diabetes mellitus. Finally, abnormally high D-lactic acid was documented after administration or ingestion of large amounts of propylene glycol, as paraneoplastic phenomenon and perhaps also in a so far poorly characterized inherited inborn error of metabolism.

Conclusions

In humans with short bowel syndrome (or carbohydrate malabsorption), D-lactic acidosis is likely rather common and under-recognized. This condition should be included in the differential diagnosis of unexplained high-gap metabolic acidosis where the anion causing the acidosis is not known. Furthermore, diabetic acidosis might be caused by accumulation of both ketone bodies and D-lactic acid. Finally, there are endogenous sources of D-lactic acid in subjects with propylene glycol intoxication.
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Metadaten
Titel
D-lactic acidosis in humans: systematic literature review
verfasst von
Davide G. A. M. Bianchetti
Giacomo S. Amelio
Sebastiano A. G. Lava
Mario G. Bianchetti
Giacomo D. Simonetti
Carlo Agostoni
Emilio F. Fossali
Gregorio P. Milani
Publikationsdatum
07.12.2017
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Nephrology / Ausgabe 4/2018
Print ISSN: 0931-041X
Elektronische ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-017-3844-8

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