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Association of serum retinol-binding protein 4 concentration with risk for and prognosis of amyotrophic lateral sclerosis

  • ALS Registry Study Group
  • University of Ulm
  • University Medical Center Ulm and Center of Excellence 'Metabolic Disorders'
  • Technical University of Munich
  • Partner Site Munich Heart Alliance
  • Universite de Strasbourg
  • Klinikum Günzburg
  • Kreiskliniken Reutlingen
  • Klinikum Sindelfingen
  • Klinikum Friedrichshafen
  • Stuttgart-Bürgerhospital and Katharinenhospital
  • ZFP Südwürttemberg Weissenau
  • Ostalb-Klinikum Aalen
  • Oberschwabenklinik Ravensburg
  • Klinik Dietenbronn
  • Klinikum am Weissenhof
  • Klinikum Ludwigsburg
  • Schmieder Kliniken Konstanz
  • University of Munich
  • Department of Psychiatry and Psychotherapy
  • ZfP Zwiefalten
  • Klinikum am Gesundbrunnen Heilbronn
  • Heidelberg University
  • Bezirkskrankenhaus Kaufbeuren
  • University of Freiburg
  • Department of Neurology
  • Kliniken Landkreis Heidenheim
  • Fachklinik Wangen
  • Klinikum Kempten
  • Kliniken Schwenningen
  • University of Würzburg
  • Schmieder Kliniken Allensbach
  • Bezirkskrankenhaus Memmingen
  • Marien Hospital Stuttgart
  • Klinikum Memmingen
  • Caritas Krankenhaus
  • German Armed Forces Hospital of Ulm
  • Weissenau Department of Neurology
  • University of Tübingen
  • Christophsbad Göppingen
  • Klinikum Augsburg
  • Vinzenz von Paul Hospital
  • Kliniken Landkreis Sigmaringen
  • EMSA Singen
  • Klinikum Winnenden
  • Kinderklinik Stadtischen K.
  • Klinik Biberach
  • Bezirkskrankenhaus Augsburg
  • Kliniken Esslingen
  • Klinikum Dietenbronn

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

IMPORTANCE Knowledge about the metabolic states of patients with amyotrophic lateral sclerosis (ALS) may provide a therapeutic approach. OBJECTIVE To investigate the association between the onset and prognosis of ALS and serum retinol-binding protein 4 (RBP4) concentration as a biomarker for insulin resistance and vitamin Ametabolism. DESIGN, SETTING, AND PARTICIPANTS Case-control design for risk factors of ALS; cohort design for prognostic factors within ALS cases. Between October 1, 2010, and June 30, 2014, a population-based case-control study with randomly selected controls was established based on the ALS Registry Swabia in southern Germany, with a target population of 8.4 million inhabitants. Response rates were 64.8%among the cases and 18.7%among the controls. The dates of analysis were April 2016 to May 2017. MAIN OUTCOMES AND MEASURES Serum sampleswere measured for RBP4. Information on covariates was assessed by an interview-based standardized questionnaire. Main outcomes and measures were adjusted odds ratios for risk of ALS associated with serum RBP4 concentration, as well as time to death associated with RBP4 concentration at baseline in ALS cases only. Conditional logistic regression was applied to calculate multivariable odds ratios for risk of ALS. Survival models were used in cases only to appraise their prognostic value. RESULTS Data from 289 patients with ALS (mean [SD] age, 65.7 [10.5] years; 172 [59.5%] male) and 504 controls (mean [SD] age, 66.3 [9.8] years; 299 [59.3%] male) were included in the case-control study. Compared with controls, ALS cases were characterized by lower body mass index, less educational attainment, smoking, light occupational work intensity, and self-reported diabetes. The median serum RBP4 concentration was lower in ALS cases than in controls (54.0 vs 59.5mg/L). In the multivariable model, increasing RBP4 concentration was associated with reduced odds for ALS (top vs bottom quartile odds ratio, 0.36; 95%CI, 0.22-0.59; P for trend <.001), which persisted after further adjustment for renal function and for leptin and adiponectin. Among 279 ALS cases during a median follow-up of 14.5 months, 104 died (mean [SD] age, 68.9 [10.3] years; 56 [53.9%] male). In this ALS cohort, an inverse association was found between serum RBP4 concentration as a continuous measure and survival. CONCLUSIONS AND RELEVANCE RBP4 was inversely related to risk for and prognosis of ALS, suggesting that vitamin Ametabolism or impaired insulin signaling could be involved. Further research, including a prospective design and other biological markers, is necessary to clarify the role of insulin resistance in the pathogenesis of ALS.

Original languageEnglish
Pages (from-to)600-607
Number of pages8
JournalJAMA Neurology
Volume75
Issue number5
DOIs
StatePublished - May 2018

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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