Approaches to themanagement
of statin intolerant patients
By
Ashraf Reda, MD,FESC
Prof and head of Card. Dep., Menofiya University
President of WGLVR
Chairman of EGYBAC
2.
The problem
• 5% -10% side effects with statin
• More patients become statin eligible
• The use of high dosage
• Combination therapy
• Special situations: Pregnancy-Elderly-Children
• Run in phases may underestimate the
problem
3.
Higher doses= Moreadverse effects
“TNT”
Non CV mortality with the high doses need further evaluation
Elevated liver enzymes:1.2% vs 0.2% p<0.001
Rhabdomyolysis 2 cases(80mg) vs 3 cases(10mg)
5461 pts. were excluded in the run in phase
4.
IDEAL Trial: SeriousAdverse Events
2.2% p<0.001
2%
p<0.001
ALT >3x upper
limit of normal
1.1%
0.97%
%
1%
0.11%
0%
Liver Enzyme Elevation Myalgia
Atorvastatin Simvastatin
Liver enzyme elevation and myalgia (%) Presented at AHA 2005
5.
Elevated Liver Enzymes:What to do?
• Less than 1%
• Usually asymptomatic
• Rarely cause Liver failure
• Reversible
• Usually improve with continuing statin or
reducing the dose
• Change to another statin is an option
6.
Muscle Symptoms
• Myalgiais the most common (1.5-3.5%)
• Myopathy: Less common (0.05%)
• Rhabdomyolysis: Serious ( 1/10000)
7.
Co-Q 10
• Mayreduce statin induced muscle symptoms
• No large well controlled studies
• Minimal side effects
Populations at risk
• Elderly > 75-80
• Small body mass index
• Hepatic or renal dysfunction
• Concomitant medications
• Large amount of Grapefruit
• Combination lipid lowering therapy
10.
Steps to Minimizethe Risk of Muscle Toxicity with Fibrate–Statin
Combination Therapy
Use statin alone for non-HDL-C goals
Use fish oils or niacin rather than fibrates
Keep the doses of the statin and fibrate low
Dose the fibrate in the AM and the statin in the PM
Avoid in renal impairment
Discontinue therapy if muscle symptoms are present and
CK is >10 times the upper limit of normal
If not toleratedwhat to do?
• DC Statin temporarily to be sure that the Side
effects are statin related
• Re-challenge with a lower dose or change to
other statin
• If multiple statins are not tolerated we can use
less effective
drugs(Resin, Ezetimibe, Niacin, Fibrate)
• More intense Life style change program
Referred because ofabnormal lipid profile
• 32 yrs female
• 30 weeks twin pregnancy
• IUF
• +ve FH (CABG for the Father @ 45yrs)
• Father T Cholesterol known to be more than
300 mg/dl
• Border line Bl. G.
• No Ho DM or hypertension
15.
Lipid profile
• 1stset : T.Ch: 320mg/dl, TGs: 580onmg/dl
• The day of exam: T ch: 310mg/dl ,TGs: 640
mg/dl
16.
Plan
• No statinduring pregnancy and lactation
• Fibrates are tumerogenic for the fetous
WHAT TO DO?
• Omega III : safe but no LDL lowering effect
• Glucose-Insulin infusion
• Immunoadsorpton session??
18.
New Statin IntoleranceClinic:
Work up
• Validated questionnaire including FH of statin
intolerance
• Level of CK and Vit. D
• Renal and thyroid function tests
• Genetic testing for statin efficacy and
potential toxicity
• Proximal muscle strength evaluation
• Percutaneous muscle biopsy
Conclusions
• Statin intoleranceis not common however the
numbers are increasing as Millions are
receiving statin
• Side effects with a statin do not mean that
other statin couldn’t be used
• Elderly, Low BMI, hepatic or renal
dysfunction, high dosage and combinations
are important predictors
22.
Immunoadsorption- LDL aphaeresis(to take away
[Greek])
Indications:
*failure medical (>LDL>200 mg/dl with CAD)
and > 300 mg/dl without CAD
*Coast s 3000 / tt every 2 weeks for life
23.
Statin in childhoodfor familial dyslipidemia
• The earlier to start the better (CIMT)
• As early as 8 years is effective and probably
safe
24.
Apo A-1 Milano
•Five weekly infusions of an ApoA-I Milano/ phospholipid
complex produced significant regression of coronary
atheroma burden by IVUS.
• Adverse events were similar to placebo.
• Coronary disease is more dynamic than previously
realized and can be rapidly affected by agents that
augment reverse cholesterol transport.
24
Characteristics of human
ApoA-IMilanoCarriers
Discovered in 1979 Limone sul Garda
•Rare R173C mutation in apoA-I
•Circulates as dimers and monomers
•HDL/apoA-I deficiency
•Mild hypertriglyceridemia
•Paradoxical resistance to heart
“Gain of Function” disease
Mutation 26
28.
With LDL 300,TG 520mg/dl start with
1. Fenofibrate
2. statin
3. Statin + Fibrate
4. Statin+ Ezetemib
29.
When liver enzymesincrease to 1.5
times base line
1. Continue with the same dose
2. Change to another statin
3. Reduce the dose
4. Replace with fibrate
30.
All are contraindicationsto statin
therapy except
1. Pregnancy
2. Lactation
3. Liver cirhosis
4. Active hepatitis
31.
All are RFfor statin muscle toxicity
except
• Age below 40 yrs
• Renal impairment
• Liver dysfunction
• Combination therapy
32.
All can improvestatin intolerance
except
• Adding Co Q10
• Giving fibrate @AM and Statin @PM
• Using 2c9 metabolized statin
• Using Cyp3A4 metabolized statin
33.
CardioEgypt 2011
1. 16-20 October
2. 17- 21 October
3. 18-22 October
4. 19-23 October