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CARDIovASCULAR RISK FACToRS: CHoLESTERoL  n  33



             emphasized throughout ATP III: the intensity   adherence  over  time  to  the  prescribed  die-
             of risk-reduction therapy should be adjusted   tary regimen. The first priority of pharmaco-
             to an individual’s absolute risk.        logical therapy is to achieve the appropriate   C
                 The Framingham projections of 10-year   LDL-C  goal  (as  defined  by  the  individual’s
             absolute  CHD  risk  (i.e.,  the  percent  proba-  category of risk). ATP III recommends the use
             bility of having a CHD event in 10 years) are   of HMG-CoA reductase inhibitors (statins) as
             used  to  identify  and  risk  stratify  individu-  first-line therapeutic agents. In a meta-anal-
             als. In addition to LDL-C, risk determinants   ysis  of  clinical  trials,  the  average  reduction
             include  presence  or  absence  of  CHD  and   in TC in more than 30,000 middle-aged men
             other  clinical  forms  of  atherosclerotic  dis-  followed for more than 5 years was 20%, the
             ease, cigarette smoking, hypertension (blood   average reduction in LDL-C was 28%, and the
             pressure ≥ 140/90 mm Hg or on antihyperten-  decline in triglyceride averaged 13% (LaRosa,
             sive  medication),  low  high-density  lipopro-  He, & vupputuri, 1999). Results of a landmark
             tein  cholesterol  (<40  mg/dl),  family  history   secondary  prevention  trial  suggested  that
             of premature CHD, and age (men ≥ 45 years,   early and continued lowering of LDL-C with
             women ≥ 55 years). The category of highest   an  intensive  lipid-lowering  (statin)  regimen
             risk (10-year risk > 20%) includes CHD and   provides greater protection against death or
             CHD  risk  equivalents  (other  clinical  forms   major cardiovascular events than a standard
             of atherosclerotic disease, diabetes) and has   regimen (Cannon et al., 2004). other pharma-
             a goal of LDL-C defined as less than 100 mg/  cological agents currently used in treatment
             dl.  The  intermediate  risk  category  (10-year   of  dyslipidemia  in  adults  include  bile–acid
             risk ≤ 20%) includes multiple (2+) risk factors   binding  resins,  niacin,  and  fibrates.  The
             and has a goal LDL-C as 130 mg/dl; the low-  decisions  to  initiate  LDL-C-lowering  drug
             est risk category (10-year risk < 10%) includes   therapy, the type and dosage of agent to be
             0  and 1 risk  factors  with an  LCL-C  goal  of   used, and the schedule for monitoring indi-
             160 mg/dl.                               vidual response to therapy are based on the
                 The cornerstone of treatment for hyper-  individual’s  baseline  risk  status.  normally,
             cholesterolemia and other lipid abnormalities   the patient’s response is evaluated approxi-
             is  TLC,  with  emphasis  on  dietary  modifi-  mately 6 weeks after starting drug therapy.
             cation, increased physical activity, and nor-  Relatedly,  TLC  continues  throughout  (and
             malization  of  body  weight.  The  important   beyond) the duration of pharmacotherapy.
             components of the TLC diet are saturated fat   Consistent  with  recommendations  of
             (<7%  of  total  calories),  polyunsaturated  fat   the 33rd Bethesda Conference on preventive
             (up to 10% of total calories), and monounsat-  cardiology  (ockene,  Hayman,  Pasternak,
             urated fat (up to 20% of total calories). Less   Schron, & Dunbar-Jacob, 2002), ATP III iden-
             than 200 mg/day of dietary cholesterol, 50%   tifies and targets adherence-enhancing inter-
             to 60% of total calories from carbohydrates,   ventions that consider the characteristics of
             and  approximately  15%  of  total  calories   the individual patient, the provider, and the
             from  protein  are  recommended.  other  key   systems  of  health  care  delivery.  Case  man-
             components of the TLC diet include viscous   agement by nurses within the context of mul-
             fiber, plant stanols/sterols, and soy protein.   tidisciplinary team approaches is considered
             Considerable variation in response to dietary   an integral component of increasing adher-
             modification has been observed in males and   ence  to  therapeutic  regimens  for  hypercho-
             females  across  the  life  span.  variations  in   lesterolemia and other lipid abnormalities.
             serum TC, for example (ranging from 3% to    The  nCEP  has  not  revised  the  1991
             14%), are attributed to individual differences   definitions  and  guidelines  for  management
             in biological mechanisms, baseline TC levels,   of  hypercholesterolemia  in  children  and
             nutrient  composition  of  baseline  diets,  and   adolescents  in  the  United  States;  however,
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