Page 939 - Equine Clinical Medicine, Surgery and Reproduction, 2nd Edition
P. 939

914                                        CHAPTER 6



  VetBooks.ir  Diagnosis                                  insulin dysregulated. Measurement of endogenous
                                                          ACTH  concentration  is  a  popular  option  to  diag-
           In addition to the clinical signs, certain changes may
           be seen in a complete blood count and on a serum
                                                          higher physiological values observed in the autumn,
           chemistry  panel  that  support  a  presumptive  diag-  nose PPID. Circannual  variability, with normal
           nosis.  These include a  mature neutrophilia,  lym-  has led to seasonal reference intervals being devel-
           phopenia and mild hyperglycaemia due to increased   oped by laboratories to help properly interpret the
           glucocorticoid secretion.                      results, especially in early stage cases.
             The pituitary gland can be visualised by advanced   The dexamethasone suppression test (Table 6.7)
           imaging techniques (computed tomography [CT]   is another common test to diagnose PPID that
           or magnetic resonance imaging [MRI]), but these   relies on the ability of an exogenous glucocorticoid
           techniques  are  not used  routinely  because of  poor   to induce a negative feedback and reduce cortisol
           reference intervals and the possible need for gen-  secretion. There is some fear that administration of
           eral anaesthesia or heavy sedation. They may also   dexamethasone to a horse with PPID and laminitis
           lack sensitivity for early detection of the disease as   might  exacerbate the latter. While the risk of this
           dysfunction of the pars intermedia of the pituitary   appears to be low and not demonstrated, many other
           gland could be observed before significant enlarge-  tests carry no risk at all. Additionally, response to
           ment occurs.                                   the  dexamethasone  suppression  test  is  not  highly
             Several tests have been described for the diagno-  repeatable and may produce false-positive and false-
           sis of PPID, but many of them have low sensitivity   negative results.
           and/or specificity. Measurement of serum cortisol   The TRH stimulation test (Table 6.8) has
           concentration is not useful as it is usually within   been developed to increase testing sensitivity in
           the reference interval. It is thought that horses with   milder cases in the months outside the autumn.
           PPID lose the normal circadian variation of serum   Stimulation of TRH receptors on the cortico-
           cortisol and it has been proposed that PPID could   tropes of the pituitary pars distalis and on the
           be diagnosed by finding a <30% decrease in serum   melanotrophs of the pars intermedia results in
           cortisol measured in the late afternoon relative to   an increase in ACTH. This increase, however, is
           measurement in the early morning. However, loss of   greater  in horses  with  PPID.  Domperidone is  a
           a circadian pattern of cortisol secretion is not spe-  dopamine receptor antagonist that can stimulate
           cific to PPID, thus using it to establish a PPID diag-  the melanotrophs of the pars distalis resulting in
           nosis would result in a high number of false-positive   an increased secretion of ACTH. In horses with
           results.                                       PPID, the oral administration of 3.3  mg/kg of
             Before  EMS  was  identified  as  a  separate  entity,   domperidone results in a larger ACTH secretion
           increased fasting serum insulin was thought to be   than in control horses.
           suggestive of PPID. Subsequently it has been shown   There is evidence that the results of diagnos-
           that PPID has no significant effect on insulin levels   tic tests, when performed on multiple occasions,
           and that less than 30% of horses with PPID were   may vary within an individual horse to the point



            Table 6.7  Protocol for the dexamethasone suppression test

               • Collect baseline plasma sample for cortisol concentration around 17.00 hours
               • Administer dexamethasone (40 μg/kg i/m)
               • Collect a plasma sample for cortisol concentration 17–19 hours later (around 10.00 hours)
               • Collection of plasma samples at 15, 19 and 23 hours may be more useful, particularly in young or mildly affected horses. Some
              horses that are just starting to manifest clinical signs of pituitary pars intermedia dysfunction may be suppressed at 8.00 hours
              or 12.00 hours noon, but are no longer suppressed by 12.00 hours noon or 16.00 hours.
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