Familial combined hyperlipidemia is the most frequent cause of primary dyslipidemia
in Mexico. Its manifestations include hypercholesterolemia, hypertriglyceridemia,
or a combination of both. Despite its high frequency, a proper diagnosis is rarely
made. Assessment of the lipid profiles of at least three first-degree relatives is
necessary. The diagnosis of familial combined hyperlipidemia in a family not only
leads to the identification of other affected family members but, more important,
allows cardiovascular risk stratification of those affected. Prospective studies have
confirmed the atherogenicity of the disease. A critical review of the current literature
in this field is presented in this article. Although three screenings of the genome
have been completed, the genes responsible for this disorder have not been identified.
Limitations with respect to the characterization of affected subjects and the heterogeneity
of the disease are among possible explanations. However, familial combined hyperlipidemia,
because of its high prevalence, must be given greater priority. It represents a great
challenge for physicians involved in the treatment of dyslipidemic patients.
KEYWORDS
Familial combined hyperlipidemia - apolipoprotein B - cholesterol - triglycerides
- HDL cholesterol
REFERENCES
- 1
Davignon J, Genest Jr J.
Genetics of lipoprotein disorders.
Endocrinol Metab Clin North Am.
1998;
27
521-550
- 2
Arner P.
Is familial combined hyperlipidaemia a genetic disorder of adipose tissue?.
Curr Opin Lipidol.
1997;
8
89-94
- 3
Bredie S J, Demacker P N, Stalenhoef A F.
1997. Metabolic and genetic aspects of familial combined hyperlipidaemia with emphasis
on low-density lipoprotein heterogeneity.
Eur J Clin Invest.
1997;
27
802-811
- 4
Goldstein J L, Schrott H G, Hazzard W T, Bierman E L, Motulsky A G.
Hyperlipidemia in coronary heart disease. II: genetic analysis of lipid levels in
176 families and delineation of a new inherited disorder, combined hyperlipidemia.
J Clin Invest.
1973;
52
1544-1568
- 5
Rose H G, Kranz P, Weinstock M, Juliano J, Haft J I.
Inheritance of combined hyperlipoproteinemia: evidence for a new lipoprotein phenotype.
Am J Med.
1973;
54
148-160
- 6
Nikkila E A, Aro A.
Family study of serum lipids and lipoproteins in coronary heratheart disease.
Lancet.
1973;
1
954-959
- 7
Erkelens D W.
Metabolic basis for hypertriglyceridaemia in familial combined hyperlipidaemia.
Eur Heart J.
1998;
19( suppl H)
H23-H26
- 8
Grundy S M, Chait A, Brunzell J D.
Familial Combined Hyperlipidemia Workshop.
Arteriosclerosis.
1987;
7
203-207
- 9
Sniderman A D, Ribalta J, Castro Cabezas M.
How should FCHL be defined and how should we think about its metabolic bases?.
Nutr Metab Cardiovasc Dis.
2001;
11
259-273
- 10
Sniderman A D, Castro-Cabezas M, Riblata J et al..
A proposal to redefine familial combined hyperlipidemia-third workshop on FCHL.
Eur J Clin Invest.
2002;
32
71-73
- 11
de Graaf J, Stalenhoef A F.
Defects of lipoprotein metabolism in familial combined hyperlipidaemia.
Curr Opin Lipidol.
1998;
9
189-196
- 12
Albers J J, Marcovina S M, Kennedy H, Mei J V, Henderson L O, Hannon W H.
International Federation of Clinical Chemistry standardization project for measurement
of apolipoproteinsA-I, and B. Comparability of apolipoprotein B values by use of International
Reference Material.
Clin Chem.
1994;
40
586-592
- 13
Bredie S J, Demacker P N, Stalenhoef A F.
1997. Metabolic and genetic aspects of familial combined hyperlipidaemia with emphasis
on low-density lipoprotein heterogeneity.
Eur J Clin Invest.
1997;
27
802-811
- 14
Valles V, Aguilar-Salinas C A, Gómez-Pérez F J et al..
Apolipoprotein B and AI distribution in the Mexican urban adults: results of a nation-wide
survey.
Metabolism.
2002;
51
560-568
- 15
McNeely M, Edwards K, Marcovina S, Brunzell J D, Motulsky A, Austin M.
Lipoprotein and apolipoprotein abnormalities in familial combined hyperlipidemia:
a 20-year prospective study.
Atherosclerosis.
2001;
159
471-481
- 16
Kwiterovich P O.
Clinical relevance of the biochemical, metabolic and genetic factors that influence
low-density lipoprotein heterogeneity.
Am J Cardiol.
2002;
90(suppl)
30i-47i
- 17
Aguilar-Salinas C A, Díaz-Polanco A, Quintana E et al..
Genetic factors play an important role in the pathogenesis of hyperlipidemia post-transplantation.
Am J Kidney Dis.
2002;
40
169-177
- 18
Sniderman A D, Wolfson C, Teng B, Franklin F A, Bachorik P S, Kwiterovich P O.
Association of hyperapobetalipoproteinemia with endogenous hypertriglyceridemia and
atherosclerosis.
Ann Intern Med.
1982;
97
833-839
- 19
Porkka K V, Nuotio I, Pajukanta P et al..
Phenotype expression in familial combined hyperlipidemia.
Atherosclerosis.
1997;
133
245-253
- 20
Hokanson J, Austin M, Zambon A, Brunzell J.
Plasma triglycerides and LDL heterogeneity in familial combined hyperlipidemia.
Arterioscler Thromb.
1993;
13
427-434
- 21
Babirak S, Brown G, Brunzell J.
Familial combined hyperlipidemia and abnormal lipoprotein lipase.
Arterioscler Thromb.
1992;
12
1176-1183
- 22
Ascaso J F, Merchante A, Lorente R, Real J T, Martinez-Valls J, Carmena R.
A study of insulin resistance using the minimal model in nondiabetic familial combined
hyperlipidemic patients.
Metabolism.
1998;
47
508-513
- 23
Meijssen S, Castro Cabezas M, Twickler T, Jansen H, Erkelens D W.
In vivo evidence of defective postprandial and postabsorptive free fatty acid metabolism
in familial combined hyperlipidemia.
J Lipid Res.
2000;
41
1096-1102
- 24
Aouizerat B E, Allayee H, Cantor R M et al..
Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol
acyltransferase on 16q.
Arterioscler Thromb Vasc Biol.
1999;
19
2730-2736
- 25
Pei W, Baron H, Muller-Myhsok B et al..
Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in
Chinese and German families.
Clin Genet.
2000;
57
29-34
- 26
Pihlajamäki J, Rissanen J, Valve R, Heikkinen S, Karjalainen L, Laakso M.
Different regulation of free fatty acid levels and glucose oxidation by the Trp64Arg
polymorphism of the beta3-adrenergic receptor gene and the promoter variant (A-3826G)
of the uncoupling protein 1 gene in familial combined hyperlipidemia.
Metabolism.
1998;
47
1397-1402
- 27
Coon H, Myers R, Borecki I et al..
Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional
heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus.
Arterioscler Thromb Vasc Biol.
2000;
20
2275-2280
- 28
Venkatesan S, Cullen P, Pacy P, Halliday D, Scott J.
Stable isotopes show a direct relation between VLDL apoB overproduction and serum
triglycerides and indicate a metabolically and biochemically coherent basis for familial
combined hyperlipidemia.
Arterioscler Thromb.
1993;
13
1110-1118
- 29
Gehrisch S, Kostka H, Tiebel M et al..
Mutations of the human hepatic lipase gene in patients with combined hypertriglyceridemia/hyperalphalipoproteinemia
and in patients with familial combined hyperlipidemia.
J Mol Med.
1999;
77
728-734
- 30
Cortner J A, Coates P M, Bennett M J, Cryer D R, Le N A.
Familial combined hyperlipidemia: use of stable isotopes to demonstrate overproduction
of very low-density lipoprotein apolipoprotein B by the liver.
J Inherit Metab Dis.
1991;
14
915-922
- 31
Pajukanta P, Porkka K, Antikainen M et al..
No evidence of linkage between familial combined hyperlipidemia and genes encoding
lipolytic enzymes in Finnish families.
Arterioscler Thromb Vasc Biol.
1997;
17
841-850
- 32
Del Rincón-Jarero J P, Aguilar-Salinas C A, Guillén-Pineda L E, Gómez Pérez F J, Rull J A.
Lack of agreement between the plasma lipid based criteria and the apoprotein B for
the diagnosis of Familial Combined Hyperlipidemia (FCHL) in members of FCHL kindreds.
Metabolism.
2002;
51
218-224
- 33
Wijsman E M, Brunzell J D, Jarvik G P, Austin M A, Motulsky A G, Deeb S S.
Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein
AI-CIII-AIV gene complex.
Arterioscler Thromb Vasc Biol.
1998;
18
215-226
- 34
Hopkins P, Heiss G, Ellison C et al..
Coronary artery disease in familial combined hyperlipidemia and familial hypertriglyceridemia.
Circulation.
2003;
108
519-523
- 35
Aguilar-Salinas Carlos A, Olaiz G, Valles V et al..
High prevalence of low HDL cholesterol concentrations and mixed hyperlipidemia in
a Mexican nation wide survey.
J Lipid Res.
2001;
42
1298-1307
- 36
Austin M, McKnight B, Edward K et al..
Cardiovascular disease mortality in familial forms of hypertriglyceridemia: a 20 year
prospective study.
Circulation.
2000;
101
2777-2782
- 37
Purnell J, Kahn S, Schwartz R, Brunzell R.
Relationship of insulin sensitivity and apoB levels to intraabdominal fat in subjects
with familial combined hyperlipidemia.
Arterioscler Thromb Vasc Biol.
2001;
21
567-572
- 38
Aguilar-Salinas C A, Barrett H P, Pulai J, Zhu X, Schonfeld G.
A familial combined hyperlipidemic kindred with impaired apolipoprotein B catabolism.
Kinetics of apolipoprotein B during placebo and pravastatin therapy.
Arterioscler Thromb Vasc Biol.
1997;
17
72-82
- 39
Chait A, Albers J J, Brunzell J D.
Very low density overproduction in genetic forms of hypertriglyceridemia.
Eur J Clin Invest.
1980;
10
161-172
- 40
Kissebah A H, Alfarsi A, Adams P W.
Integrated regulation of very low density lipoprotein triglycerides and apolipoprotein
B kinetics in man: normolipidemic subjects, familial hypertriglyceridemia and familial
combined hyperlipidemia.
Metabolism.
1981;
30
856-868
- 41
Allayee H, Dominguez K M, Aouizerat B E et al..
Contribution of the hepatic lipase gene to the atherogenic lipoprotein phenotype in
familial combined hyperlipidemia.
J Lipid Res.
2000;
41
245-252
- 42
Ayyobi A F, McGladdery S H, McNeely M J, Austin M A, Motulsky A G, Brunzell J D.
Small, dense LDL and elevated apolipoprotein B are the common characteristics for
the three major lipid phenotypes of familial combined hyperlipidemia.
Arterioscler Thromb Vasc Biol.
2003;
23
1289-1294
- 43
Vakkilainen J, Jauhiainen M, Yliatalo K et al..
LDL particle size in familial combined hyperlipidemia; effects of serum lipid, lipoprotein-modifying
enzymes and lipid transfer proteins.
J Lipid Res.
2002;
43
598-603
- 44
Pajukanta P, Terwilliger J D, Perola M et al..
Genomewide scan for familial combined hyperlipidemia genes in Finnish families, suggesting
multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein
B levels.
Am J Hum Genet.
1999;
64
1453-1463
- 45
Tahvanainen E, Pajukanta P, Porkka K et al..
1998. Haplotypes of the ApoA-I/C-III/A-IV gene cluster and familial combined hyperlipidemia.
Arterioscler Thromb Vasc Biol.
1998;
18
1810-1817
- 46
Pennacchio L A, Rubin E M.
Apolipoprotein A5, a newly identified gene that affects plasma triglyceride levels
in humans and mice.
Arterioscler Thromb Vasc Biol.
2003;
23
529-534
Carlos Alberto Aguilar SalinasM.D.
Vasco de Quiroga 15, Mexico City 14000, Mexico