Page 313 - Vitamin D and Cancer
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300                                                     M. Fakih et al.

            Fig. 13.3  Cholecalciferol   8
            dose effect and time course                   2000IU
            of changes in serum 24,
            25-D  levels in colorectal   6                400IU
               3
            cancer patients. Serum 24,25-
            D  levels determined by
             3
            atmospheric pressure chemi-  Serum 24,25-D 3  (ng/mL)  4
            cal ionization (APCI) in posi-
            tive ion mode LC/MS/MS.
            Data = mean + SEM         2


                                      0
                                        0      2       4      6      8      10
                                                     Time (months)


            and time course of the changes in serum 24, 25-D  in this cohort of colorectal can-
                                                    3
            cer patients is shown in Fig. 13.3. These results suggest that comprehensive profiles
            of serum vitamin D  metabolite in cancer patients are now achievable.
                            3

            13.1.2.3   Vitamin D Status and Adenomatous Polyps

            Several studies suggest a correlation between vitamin D intake or 25-hydroxy vita-
            min D (25-D ) status and the risk of adenomatous polyps (Table 13.1). Levine et al.
                      3
            conducted a case–control study where 473 patients with a finding of at least one
            adenoma on initial sigmoidoscopy were compared to controls without any polyps
            on sigmoidoscopy or without any prior history of adenoma [33]. Plasma 25-D  was
                                                                          3
            assayed  by  a  competitive  binding  assay.  Increasing  plasma  levels  of  25-D   was
                                                                          3
            associated with a decreased risk of adenoma (OR = 0.74 for the highest quartile
            compared to lowest; CI 0.49–1.09). The benefit from higher serum 25-D  was more
                                                                     3
            pronounced in the population with lower calcium intake. In another case–control
            study, 222 patients with newly diagnosed adenomas on colonoscopy were com-
            pared to 479 controls who had adenoma-free colonoscopies [34]. One hundred and
            eleven  cases  and  238  controls  had  available  serum  for  25-D   assay  by  enzyme
                                                              3
            immunoassay. A significant association was present between the highest tertile of
            25-D  and a lower risk of adenoma in comparison to the lowest tertile (OR 0.51; CI
                3
            0.27–0.98).  Contrary  to  the  findings  by  Levine,  the  benefit  noted  on  this  study
            seemed more pronounced in the population with a higher calcium intake. In the
            third study, 239 patients with colonic adenomas diagnosed by sigmoidoscopy were
            compared  to  228  controls  with  an  adenoma-free  sigmoidoscopy  [35].  25-D ,
                                                                             3
            assayed  by  RIA,  was  found  protective  against  adenoma  formation,  with  a  risk
            reduction  by  26%  for  each  10  ng/mL  increase  in  serum  levels.  Only  one  study
            failed to show a clear association between 25-D  and polyps [36]. In this study,
                                                    3
            cases  and  controls  were  drawn  from  the  Nurse’s  Health  Study.  Cases  were
              diagnosed to have at least one adenoma by endoscopy and were compared with
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