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Effect of optimized cholecalciferol and calcium intakes on bone mineral density: a randomized controlled trial in adult burns during sequelae stage.

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Academic year: 2021

Partager "Effect of optimized cholecalciferol and calcium intakes on bone mineral density: a randomized controlled trial in adult burns during sequelae stage."

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INTRODUCTION

MATERIAL AND METHODS

RESULTS

CONCLUSIONS

Method   Normal  ranges  

25OH-­‐D  (calcidiol)   Liaison®  (Diasorin®)   30-­‐80  ng/ml  

3rd  genera5on  PTH   Liaison®  (Diasorin®)   4-­‐26  pg/ml  

Total  Calcium  (Ca)   Cobas®  (Roche®)   2.15-­‐2.6  mmol/l  

M0     Bu rn  injur y     (bur n   su rf ac e   ar ea   >   20 % )   O ste op or os is   ImmobilizaMon  

Albumin-­‐related  aluminium  exposure   Systemic  inflammatory  response  

Endogenous  glucocorMcoïds  producMon  

Vitamin  D  metabolism  dysfunc5on  

Sun  exposure  limitaMon   Scar  impaired  biosyntheMc  funcMon   Ca  –  PTH  axis  abnormaliMes  

BURN  RELATED  HYPOVITAMINOSIS  D  

°  Data  mainly  concern  children  and  focused  on  ergocalciferol  supplementaMon    

AIM  OF  THE  PRESENT  RANDOMIZED  CONTROLLED  TRIAL  

°  To  assess  effect  of  a  1  year  cholecalciferol  (VD3)  and  calcium  (Ca)  subsMtuMon  on  bone  mineral  density  in  adult  burns  during  sequelae  stage  

è 

Despite  increasing  25OH-­‐D  levels  around  40ng/ml,  a  1y  treatment  combining  high  VD3  doses  and            

op5mized  Ca  intakes  failed  to  increase  T-­‐score  in  adult  burns  in  sequelae  stage.  

è 

Occurrence  of  osteopenia  in  young  burn  adults  is  worrying  in  such  context:  individualized  and  

alterna5ve  approaches  should  be  inves5gated.  

Effect  of  op5mized  cholecalciferol  and  calcium  intakes  on  bone  

mineral  density  :  a  RCT  in  adult  burns  during  sequelae  stage.  

 

AF  Rousseau

1

,  M  Foidart-­‐Dessalle

2

,  C  Remy

1

,  D  Ledoux

1

,  P  Damas

1

,  E  Cavalier

3

 

 

1Burn  Centre  and  General  Intensive  Care  Department,  2Physical  Medicine  Department,  3Clinical  Chemistry  

University  Hospital,  University  of  Liège,  Liège,  Belgium  

 

Protocol  duraMon  :  one  year  

GROUP  D:    

200000  IU  VD3/3  months  (IM)   500-­‐1000mg  Ca/day  (PO)  <-­‐>  basal  daily  intakes  

GROUP  P:  

placebo    

M0  

M12  

INCLUSION:  

°Adults  >  18y  

°Thermal  burns  daMng   from  2-­‐5y  

 

EXCLUSION:    

°  Liver  or  renal  failure   °  Prior  vitamin  D  

subsMtuMon  

°  regular  exposure  to   UVB  

°  corMcosteroids  or   anMepilepMc  

°  CV  disease,  muscle   or  skeletal  injury  

   

DATA  ANALYSIS    

°  Data  expressed  as  

median  (min-­‐max)     °  Comparisons  using   Mann-­‐Whitney  or   Wilcoxon  tests    

°  CorrelaMon  using  non   parametric  Spearman   test  

 

°  p<0.05  :  significant  

Dual  X-­‐Ray  absorp5ometry  (DXA)  :  lumbar  spine  and  femoral  neck  

 °  Results  expressed  as  T-­‐score  

 °  Reference  site  :  spine  if  <50y,  hip  if  ≥  50y  

M12    

Demographic  data   Group  P   Group  D  

Sex  ra5o  (M/F)   4/3   7/1  

Age  (y)   54  (29-­‐64)   46  (25-­‐58)  

Weight  (kg)   91  (55-­‐118)   76  (48-­‐100)  

BMI  (kg/m2)   31.2  (19.3-­‐38.1)   25.1  (18.5-­‐31.1)  

Burn  surface  area  (BSA)  (%)   30  (10-­‐55)   32.5  (10-­‐60)  

Time  since  discharge  (y)   3  (2-­‐5)   2.75  (2-­‐5)  

In-­‐hospital  length  of  stay  (months)   2  (0.2-­‐6)   3  (0.25-­‐4)  

Daily  Ca  intakes  (mg)   604  (472-­‐1947)   558  (93-­‐1053)  

15  pa5ents  included     Hypovitainosis  D  (25OH-­‐D   <30ng/ml)  in  86.6%   25OH-­‐D  levels:   -­‐  Group  P:  13  (7-­‐36)ng/ml   -­‐  Group  D:  21  (10-­‐30)ng/ml   PTH  levels:   -­‐  Group  P:  41  (29-­‐77)pg/ml   -­‐  Group  D:  23  (13-­‐50)pg/ml  

Ca  within  normal  ranges  in  both  

groups    

Osteopenia  (T-­‐score  ≤  -­‐1)  in  53%  

(of  which  3  men  <  40y)  

T  score:  

-­‐  Group  P:  -­‐0.5  (-­‐2.9  -­‐  +1.4)   -­‐  Group  D:  -­‐1  (-­‐1.9  -­‐  +1.5)   No  correlaMon  between  BSA  and  iniMal  T-­‐score  

    25OH-­‐D  levels:   -­‐  Group  P:  15  (8-­‐39)ng/ml   -­‐  Group  D:  40  (37-­‐61)ng/ml      (p=0.0078)    

No  significant  varia5on  in  PTH   and  Ca  levels  

         

No  significant  increase  in  T-­‐score  

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