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{{Short description|Genetic disorder in fat handling}}
{{Infobox medical condition (new)
{{Infobox medical condition (new)
| name = Lipoprotein lipase deficiency
| image = Autosomal recessive - en.svg
| name = Lipoprotein lipase deficiency
| caption = Lipoprotein lipase deficiency is inherited via autosomal recessive manner
| image = Autosomal recessive - en.svg
| caption = Lipoprotein lipase deficiency is inherited via autosomal recessive manner
| image_size = 220px
| image_size = 220px
| pronounce =
| pronounce =
| field =
| field =
⚫
| synonyms = LPLD; familial chylomicronemia syndrome,<ref name="Santamarina-Fojo">{{cite journal|last=Santamarina-Fojo|first=S|title=Familial lipoprotein lipase deficiency.| journal=Endocrinol Metab Clin North Am|date=1998|volume=27|issue=3|pages=551–567|pmid=9785052|doi=10.1016/S0889-8529(05)70025-6}}</ref> chylomicronemia,<ref name="Andrews">{{cite book |author=James, William D. |author2=Berger, Timothy G.|title=Andrews' Diseases of the Skin: clinical Dermatology |publisher=Saunders Elsevier |year=2006 |isbn=978-0-7216-2921-6 |oclc=62736861 |display-authors=etal}}</ref>{{rp|533}} chylomicronemia syndrome,<ref name=Bolognia>{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=[[Mosby (publisher)|Mosby]] |location=St. Louis |year=2007 |isbn=978-1-4160-2999-1 |oclc=212399895 }}</ref> familial hyperchylomicronemia, familial hyperchylomicronemia syndrome,<ref name="pmid-1992190">{{cite journal |last1=Santamarina-Fojo |first1=S |last2=Brewer HB |first2=Jr |title=The familial hyperchylomicronemia syndrome. New insights into underlying genetic defects. |journal=JAMA |date=20 February 1991 |volume=265 |issue=7 |pages=904–8 |doi=10.1001/jama.1991.03460070086049 |pmid=1992190}}</ref> [[hyperlipoproteinemia]] type Ia.,<ref>{{OMIM|238600|HYPERLIPOPROTEINEMIA, TYPE I}}, updated 03/18/2004. As of October 2012, mention of type Ia no longer appears in the OMIM record.</ref> type I hyperlipoproteinemia<ref>{{cite web |title=Familial lipoprotein lipase deficiency: MedlinePlus Medical Encyclopedia |url=https://medlineplus.gov/ency/article/000408.htm |website=medlineplus.gov |access-date=17 April 2019 |language=en}}</ref>
| synonyms = Type I hyperlipoproteinemia<ref>{{cite web |title=Familial lipoprotein lipase deficiency: MedlinePlus Medical Encyclopedia |url=https://medlineplus.gov/ency/article/000408.htm |website=medlineplus.gov |accessdate=17 April 2019 |language=en}}</ref>
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| causes = Genetic
| causes = Genetic
| risks =
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}}
}}
'''Lipoprotein lipase deficiency''' is a [[genetic disorder]] in which a person has a defective gene for [[lipoprotein lipase]], which leads to very high [[triglyceride]]s, which in turn causes stomach pain and [[xanthomata|deposits of fat]] under the skin, and which can lead to problems with the [[pancreas]] and [[liver]], which in turn can lead to [[Diabetes mellitus|diabetes]]. The disorder only occurs if a child acquires the defective gene from both parents (it is [[autosomal recessive]]). It is managed by restricting [[fat]] in diet to less than 20 g/day.<ref name=GeneReviews>{{cite book |last1=Burnett |first1=John R. |last2=Hooper |first2=Amanda J. |last3=Hegele |first3=Robert A. |editor1-last=Adam |editor1-first=MP |editor2-last=Ardinger |editor2-first=HH |editor3-last=Pagon |editor3-first=RA |display-editors=etal|title=GeneReviews |date=June 22, 2017 |publisher=University of Washington |location=Seattle |chapter-url=https://www.ncbi.nlm.nih.gov/books/NBK1308/ |chapter=Familial Lipoprotein Lipase Deficiency}}</ref>
'''Lipoprotein lipase deficiency''' is a [[genetic disorder]] in which a person has a defective gene for [[lipoprotein lipase]], which leads to very high [[triglyceride]]s, which in turn causes stomach pain and [[xanthomata|deposits of fat]] under the skin, and which can lead to problems with the [[pancreas]] and [[liver]], which in turn can lead to [[Diabetes mellitus|diabetes]]. The disorder only occurs if a child acquires the defective gene from both parents (it is [[autosomal recessive]]). It is managed by restricting [[fat]] in diet to less than 20 g/day.<ref name=GeneReviews>{{cite book |last1=Burnett |first1=John R. |last2=Hooper |first2=Amanda J. |last3=Hegele |first3=Robert A. |editor1-last=Adam |editor1-first=MP |editor2-last=Ardinger |editor2-first=HH |editor3-last=Pagon |editor3-first=RA |display-editors=etal|title=GeneReviews |date=June 22, 2017 |publisher=University of Washington |location=Seattle |chapter-url=https://www.ncbi.nlm.nih.gov/books/NBK1308/ |chapter=Familial Lipoprotein Lipase Deficiency|pmid=20301485 }}</ref>

⚫
The condition has also been called familial chylomicronemia syndrome,<ref name="Santamarina-Fojo">{{cite journal|last=Santamarina-Fojo|first=S|title=Familial lipoprotein lipase deficiency.| journal=Endocrinol Metab Clin North Am|date=1998|volume=27|issue=3|pages=551–567|pmid=9785052|doi=10.1016/S0889-8529(05)70025-6}}</ref> chylomicronemia,.<ref name="Andrews">{{cite book |author=James, William D. |author2=Berger, Timothy G.|title=Andrews' Diseases of the Skin: clinical Dermatology |publisher=Saunders Elsevier |location= |year=2006 |isbn=978-0-7216-2921-6 |oclc=62736861 |display-authors=etal}}</ref>{{rp|533}} chylomicronemia syndrome,<ref name=Bolognia>{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=[[Mosby (publisher)|Mosby]] |location=St. Louis |year=2007 |isbn=978-1-4160-2999-1 |oclc=212399895 }}</ref> and [[hyperlipoproteinemia]] type Ia.<ref>{{OMIM|238600|HYPERLIPOPROTEINEMIA, TYPE I}}, updated 03/18/2004. As of October 2012, mention of type Ia no longer appears in the OMIM record.</ref>


== Signs and symptoms ==
== Signs and symptoms ==
The disease often presents in infancy with colicky pain, failure to thrive, and other symptoms and signs of the chylomicronemia syndrome. In women the use of estrogens or first pregnancy are also well known trigger factors for initial manifestation of LPLD. At all ages, the most common clinical manifestation is recurrent abdominal pain and acute [[pancreatitis]]. The pain may be epigastric, with radiation to the back, or it may be diffuse, with the appearance of an emergent [[acute abdomen]]. Other typical symptoms are eruptive xanthomas (in about 50% of patients), lipemia retinalis and hepatosplenomegaly.
The disease often presents in infancy with colicky pain, failure to thrive, and other symptoms and signs of the chylomicronemia syndrome. In women the use of estrogens or first pregnancy are also well known trigger factors for initial manifestation of LPLD. At all ages, the most common clinical manifestation is recurrent abdominal pain and acute [[pancreatitis]]. The pain may be epigastric, with radiation to the back, or it may be diffuse, with the appearance of an emergent [[acute abdomen]]. Other typical symptoms are eruptive xanthomas (in about 50% of patients), [[lipaemia retinalis]] and hepatosplenomegaly.{{citation needed|date=September 2020}}


===Complications===
''Complications:'' Patients with LPLD are at high risk of acute pancreatitis, which can be life-threatening, and can lead to chronic [[Exocrine pancreatic insufficiency|pancreatic insufficiency]] and [[Diabetes mellitus|diabetes]].
Patients with LPLD are at high risk of acute pancreatitis, which can be life-threatening, and can lead to chronic [[Exocrine pancreatic insufficiency|pancreatic insufficiency]] and [[Diabetes mellitus|diabetes]].{{citation needed|date=June 2021}}


== Diagnosis ==
== Diagnosis ==
Lab tests show massive accumulation of [[chylomicron]]s in the plasma and corresponding severe [[hypertriglyceridemia]]. Typically, the plasma in a fasting blood sample appears creamy (plasma lactescence).{{mcn|date=July 2018}}
Lab tests show massive accumulation of [[chylomicron]]s in the plasma and corresponding severe [[hypertriglyceridemia]]. Typically, the plasma in a fasting blood sample appears creamy (plasma lactescence).{{medcn|date=July 2018}}


Familial LPL deficiency should be considered in anyone with severe hypertriglyceridemia and the chylomicronemia syndrome. The absence of secondary causes of severe hypertriglyceridemia (like e.g. diabetes, alcohol, [[estrogen]]-, [[glucocorticoid]]-, [[antidepressant]]- or [[isotretinoin]]-therapy, certain [[Antihypertensive drug|antihypertensive agents]], and paraproteinemic disorders) increases the possibility of LPL deficiency. In this instance besides LPL also other loss-of-function mutations in genes that regulate catabolism of triglyceride-rich lipoproteins (like e.g. [[Apolipoprotein C2|ApoC2]], [[APOA5|ApoA5]], LMF-1, GPIHBP-1 and GPD1) should also be considered
Familial LPL deficiency should be considered in anyone with severe hypertriglyceridemia and the chylomicronemia syndrome. The absence of secondary causes of severe hypertriglyceridemia (like e.g. diabetes, alcohol, [[estrogen]]-, [[glucocorticoid]]-, [[antidepressant]]- or [[isotretinoin]]-therapy, certain [[Antihypertensive drug|antihypertensive agents]], and paraproteinemic disorders) increases the possibility of LPL deficiency. In this instance besides LPL also other loss-of-function mutations in genes that regulate catabolism of triglyceride-rich lipoproteins (like e.g. [[Apolipoprotein C2|ApoC2]], [[APOA5|ApoA5]], LMF-1, GPIHBP-1 and GPD1) should also be considered{{citation needed|date=June 2021}}


The diagnosis of familial lipoprotein lipase deficiency is finally confirmed by detection of either [[Dominance (genetics)|homozygous]] or [[Compound heterozygosity|compound heterozygous]] pathogenic gene variants in ''LPL'' with either low or absent lipoprotein lipase enzyme activity.
The diagnosis of familial lipoprotein lipase deficiency is finally confirmed by detection of either [[Dominance (genetics)|homozygous]] or [[Compound heterozygosity|compound heterozygous]] pathogenic gene variants in ''LPL'' with either low or absent lipoprotein lipase enzyme activity.{{citation needed|date=June 2021}}


'''Lipid measurements'''
'''Lipid measurements'''


· Milky, lipemic plasma revealing severe hyperchylomicronemia;
· Milky, lipemic plasma revealing severe hyperchylomicronemia;{{citation needed|date=September 2020}}


· Severely elevated fasting plasma triglycerides (>2000&nbsp;mg/dL);
· Severely elevated fasting plasma triglycerides (>2000&nbsp;mg/dL);{{citation needed|date=September 2020}}


'''LPL enzyme'''
'''LPL enzyme'''


· Low or absent LPL activity in post-[[heparin]] plasma;
· Low or absent LPL activity in post-[[heparin]] plasma;{{citation needed|date=June 2021}}


· LPL mass level reduced or absent in post-heparin plasma;
· LPL mass level reduced or absent in post-heparin plasma;{{citation needed|date=June 2021}}


'''Molecular genetic testing'''
'''Molecular [[genetic testing]]'''
The LPL gene is located on the short (p) arm of [[Chromosome 8 (human)|chromosome 8]] at position 22. More than 220 [[mutation]]s in the LPL gene have been found to cause familial lipoprotein lipase deficiency so far.
The LPL gene is located on the short (p) arm of [[Chromosome 8 (human)|chromosome 8]] at position 22. More than 220 [[mutation]]s in the LPL gene have been found to cause familial lipoprotein lipase deficiency so far.{{citation needed|date=June 2021}}


==Treatment==
==Treatment==
Treatment of LPLD has two different objectives: immediate prevention of pancreatitis attacks and long term reduction of cardiovascular disease risk. Treatment is mainly based on medical nutrition therapy to maintain plasma triglyceride concentration below 11,3&nbsp;mmol/L (1000&nbsp;mg/dL). Maintenance of triglyceride levels below 22,6&nbsp;mmol/L (2000&nbsp;mg/dL) prevents in general from recurrent abdominal pain.
Treatment of LPLD has two different objectives: immediate prevention of pancreatitis attacks and long-term reduction of cardiovascular disease risk.


[[Olezarsen]] (Tryngolza) was approved for medical use in the United States in December 2024.<ref>{{cite press release | title=Tryngolza (olezarsen) approved in U.S. as first-ever treatment for adults living with familial chylomicronemia syndrome as an adjunct to diet | publisher=Ionis Pharmaceuticals | via=PR Newswire | date=19 December 2024 | url=https://www.prnewswire.com/news-releases/tryngolza-olezarsen-approved-in-us-as-first-ever-treatment-for-adults-living-with-familial-chylomicronemia-syndrome-as-an-adjunct-to-diet-302336747.html | access-date=20 December 2024}}</ref>
'''Strict low fat diet and avoidance of simple [[carbohydrate]]s'''


⚫
=== Gene therapy ===
Restriction of dietary fat to not more than 20 g/day or 15% of the total energy intake is usually sufficient to reduce plasma triglyceride concentration, although many patients report that to be symptom free a limit of less than 10g/day is optimal. Simple carbohydrates should be avoided as well. Medium-chain triglycerides can be used for cooking, because they are absorbed into the [[Hepatic portal vein|portal vein]] without becoming incorporated into chylomicrons. Fat-soluble [[Vitamin A|vitamins A]], [[Vitamin D|D]], [[Vitamin E|E]], and [[Vitamin K|K]], and minerals should be supplemented in patients with recurrent pancreatitis since they often have deficiencies as a result of malabsorption of fat. However, the diet approach is difficult to sustain for many of the patients.
⚫
In 2012, the European Commission approved [[alipogene tiparvovec]] (Glybera), a [[gene therapy]] for adults with familial LPLD (confirmed by genetic testing) and having severe or multiple pancreatitis attacks despite dietary fat restrictions. It is the first gene therapy to receive marketing authorization in the European Union; it was priced at about $1 million per treatment, and as of 2016, only one person had been treated with it commercially.<ref name=MIT-TR2016>{{cite news|last1=Regalado|first1=Antonio|title=The World's Most Expensive Medicine Is a Bust|url=https://www.technologyreview.com/s/601165/the-worlds-most-expensive-medicine-is-a-bust/amp/|work=MIT Technology Review|date=May 4, 2016 }}</ref> A total of 31 people were treated with Glybera, most for free in clinical trials before it was taken off the market.<ref>{{cite web |url=https://newsinteractives.cbc.ca/longform/glybera/ |title=The million-dollar drug |last=Crowe |first=Kelly |date=17 November 2018 |website=CBCNews |publisher=CBC (Canadian Broadcasting Corporation) |access-date=17 November 2018 }}</ref>

'''Lipid lowering drugs'''

[[Lipid-lowering agent]]s such as [[fibrate]]s and [[Omega-3 fatty acid|omega-3-fatty acids]] can be used to lower TG levels in LPLD; however, those drugs are very often not effective enough to reach treatment goals in LPLD patients. [[Statin]]s should be considered to lower elevated non-[[High-density lipoprotein|HDL-Cholesterol]].

Additional measures are avoidance of agents known to increase endogenous triglyceride levels, such as alcohol, estrogens, [[diuretic]]s, isotretinoin, antidepressants (e.g. sertraline) and [[Adrenergic receptor|b-adrenergic]] blocking agents.

⚫
'''Gene therapy'''

⚫
In 2012, the European Commission approved [[alipogene tiparvovec]] (Glybera), a [[gene therapy]] for adults diagnosed with familial LPLD (confirmed by genetic testing) and suffering from severe or multiple pancreatitis attacks despite dietary fat restrictions. It was the first gene therapy to receive marketing authorization in Europe; it was priced at about $1 million per treatment, and as of 2016, only one person had been treated with it commercially.<ref name=MIT-TR2016>{{cite news|last1=Regalado|first1=Antonio|title=The World's Most Expensive Medicine Is a Bust|url=https://www.technologyreview.com/s/601165/the-worlds-most-expensive-medicine-is-a-bust/amp/|work=MIT Technology Review|date=May 4, 2016|language=en}}</ref> A total of 31 patients were treated with Glybera, most for free in clinical trials before the drug was taken off the market.<ref>{{cite web |url=https://newsinteractives.cbc.ca/longform/glybera/ |title=The million-dollar drug |last=Crowe |first=Kelly |date=17 November 2018 |website=CBCNews |publisher=CBC (Canadian Broadcasting Corporation) |access-date=17 November 2018 |quote=How a Canadian medical breakthrough that was 30 years in the making became the world’s most expensive drug — and then quickly disappeared}}</ref>


==Incidence==
==Incidence==
The disorder affects about 1 out of 1,000,000 people;<ref name=PMH>{{Cite book |editor1-last=Dugdale, III |editor1-first=David C. |editor2-first=David |editor2-last=Zieve |publication-date=May 29, 2011 |title=Familial lipoprotein lipase deficiency |work=[[A.D.A.M. Medical Encyclopedia]] |publisher=[[National Center for Biotechnology Information]] |url=https://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001445/ |accessdate=October 15, 2012 |author1=A.D.A.M. Editorial Board |date=2011-05-29 }}</ref> however, epidemiological data are limited and there are regional differences due to cofounder effect (e.g. in Canada) or intermarriage.
The disorder affects about 1 out of 1,000,000 people;<ref name=PMH>{{Cite book |editor1-last=Dugdale, III |editor1-first=David C. |editor2-first=David |editor2-last=Zieve |publication-date=May 29, 2011 |title=Familial lipoprotein lipase deficiency |work=[[A.D.A.M. Medical Encyclopedia]] |publisher=[[National Center for Biotechnology Information]] |url=https://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001445/ |access-date=October 15, 2012 |author1=A.D.A.M. Editorial Board |date=2011-05-29 }}</ref> however, epidemiological data are limited and there are regional differences due to cofounder effect (e.g. in Canada) or intermarriage.


== See also ==
== See also ==
Line 82: Line 73:
{{reflist}}
{{reflist}}


== Further reading==
==Further reading==
* {{cite journal |last1=Gaudet |first1=D |last2=de Wal |first2=J |last3=Tremblay |first3=K |last4=Déry |first4=S |last5=van Deventer |first5=S |last6=Freidig |first6=A |last7=Brisson |first7=D |last8=Méthot |first8=J |title=Review of the clinical development of alipogene tiparvovec gene therapy for lipoprotein lipase deficiency. |journal=Atherosclerosis. Supplements |date=June 2010 |volume=11 |issue=1 |pages=55–60 |doi=10.1016/j.atherosclerosissup.2010.03.004 |pmid=20427244}}
* {{cite journal |last1=Gaudet |first1=D |last2=de Wal |first2=J |last3=Tremblay |first3=K |last4=Déry |first4=S |last5=van Deventer |first5=S |last6=Freidig |first6=A |last7=Brisson |first7=D |last8=Méthot |first8=J |title=Review of the clinical development of alipogene tiparvovec gene therapy for lipoprotein lipase deficiency. |journal=Atherosclerosis. Supplements |date=June 2010 |volume=11 |issue=1 |pages=55–60 |doi=10.1016/j.atherosclerosissup.2010.03.004 |pmid=20427244}}
* {{cite web |title=LPL gene |url=http://ghr.nlm.nih.gov/gene/LPL |publisher=NIH Genetics Home Reference |language=en |date=February 2015}}
* {{cite web |title=LPL gene |url=http://ghr.nlm.nih.gov/gene/LPL |publisher=NIH Genetics Home Reference |language=en |date=February 2015}}
Line 89: Line 80:
== External links ==
== External links ==
{{Medical resources
{{Medical resources
| DiseasesDB = 4697
| DiseasesDB = 4697
| ICD10 = {{ICD10|E|78||e|78}}
| ICD10 = {{ICD10|E|78||e|78}}
| ICD9 =
| ICD9 =
| ICDO =
| ICDO =
| OMIM = 238600
| OMIM = 238600
| MedlinePlus = 000408
| MedlinePlus = 000408
| eMedicineSubj =
| eMedicineSubj =
| eMedicineTopic =
| eMedicineTopic =
| MeshID = D008072
| MeshID = D008072
| Orphanet = 444490
| Orphanet = 444490
| GeneReviewsNBK = NBK1308
| GeneReviewsNBK = NBK1308
| GeneReviewsName = Familial Lipoprotein Lipase Deficiency
| GeneReviewsName = Familial Lipoprotein Lipase Deficiency
}}
}}




{{Lipid metabolism disorders}}
{{Lipid metabolism disorders}}

Latest revision as of 20:17, 20 December 2024

Lipoprotein lipase deficiency
Other namesLPLD; familial chylomicronemia syndrome,[1] chylomicronemia,[2]: 533  chylomicronemia syndrome,[3] familial hyperchylomicronemia, familial hyperchylomicronemia syndrome,[4] hyperlipoproteinemia type Ia.,[5] type I hyperlipoproteinemia[6]
Lipoprotein lipase deficiency is inherited via autosomal recessive manner
SpecialtyEndocrinology Edit this on Wikidata
CausesGenetic

Lipoprotein lipase deficiency is a genetic disorder in which a person has a defective gene for lipoprotein lipase, which leads to very high triglycerides, which in turn causes stomach pain and deposits of fat under the skin, and which can lead to problems with the pancreas and liver, which in turn can lead to diabetes. The disorder only occurs if a child acquires the defective gene from both parents (it is autosomal recessive). It is managed by restricting fat in diet to less than 20 g/day.[7]

Signs and symptoms

[edit]

The disease often presents in infancy with colicky pain, failure to thrive, and other symptoms and signs of the chylomicronemia syndrome. In women the use of estrogens or first pregnancy are also well known trigger factors for initial manifestation of LPLD. At all ages, the most common clinical manifestation is recurrent abdominal pain and acute pancreatitis. The pain may be epigastric, with radiation to the back, or it may be diffuse, with the appearance of an emergent acute abdomen. Other typical symptoms are eruptive xanthomas (in about 50% of patients), lipaemia retinalis and hepatosplenomegaly.[citation needed]

Complications

[edit]

Patients with LPLD are at high risk of acute pancreatitis, which can be life-threatening, and can lead to chronic pancreatic insufficiency and diabetes.[citation needed]

Diagnosis

[edit]

Lab tests show massive accumulation of chylomicrons in the plasma and corresponding severe hypertriglyceridemia. Typically, the plasma in a fasting blood sample appears creamy (plasma lactescence).[medical citation needed]

Familial LPL deficiency should be considered in anyone with severe hypertriglyceridemia and the chylomicronemia syndrome. The absence of secondary causes of severe hypertriglyceridemia (like e.g. diabetes, alcohol, estrogen-, glucocorticoid-, antidepressant- or isotretinoin-therapy, certain antihypertensive agents, and paraproteinemic disorders) increases the possibility of LPL deficiency. In this instance besides LPL also other loss-of-function mutations in genes that regulate catabolism of triglyceride-rich lipoproteins (like e.g. ApoC2, ApoA5, LMF-1, GPIHBP-1 and GPD1) should also be considered[citation needed]

The diagnosis of familial lipoprotein lipase deficiency is finally confirmed by detection of either homozygous or compound heterozygous pathogenic gene variants in LPL with either low or absent lipoprotein lipase enzyme activity.[citation needed]

Lipid measurements

· Milky, lipemic plasma revealing severe hyperchylomicronemia;[citation needed]

· Severely elevated fasting plasma triglycerides (>2000 mg/dL);[citation needed]

LPL enzyme

· Low or absent LPL activity in post-heparin plasma;[citation needed]

· LPL mass level reduced or absent in post-heparin plasma;[citation needed]

Molecular genetic testing The LPL gene is located on the short (p) arm of chromosome 8 at position 22. More than 220 mutations in the LPL gene have been found to cause familial lipoprotein lipase deficiency so far.[citation needed]

Treatment

[edit]

Treatment of LPLD has two different objectives: immediate prevention of pancreatitis attacks and long-term reduction of cardiovascular disease risk.

Olezarsen (Tryngolza) was approved for medical use in the United States in December 2024.[8]

Gene therapy

[edit]

In 2012, the European Commission approved alipogene tiparvovec (Glybera), a gene therapy for adults with familial LPLD (confirmed by genetic testing) and having severe or multiple pancreatitis attacks despite dietary fat restrictions. It is the first gene therapy to receive marketing authorization in the European Union; it was priced at about $1 million per treatment, and as of 2016, only one person had been treated with it commercially.[9] A total of 31 people were treated with Glybera, most for free in clinical trials before it was taken off the market.[10]

Incidence

[edit]

The disorder affects about 1 out of 1,000,000 people;[11] however, epidemiological data are limited and there are regional differences due to cofounder effect (e.g. in Canada) or intermarriage.

See also

[edit]

References

[edit]
  1. ^ Santamarina-Fojo, S (1998). "Familial lipoprotein lipase deficiency". Endocrinol Metab Clin North Am. 27 (3): 551–567. doi:10.1016/S0889-8529(05)70025-6. PMID 9785052.
  2. ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6. OCLC 62736861.
  3. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1. OCLC 212399895.
  4. ^ Santamarina-Fojo, S; Brewer HB, Jr (20 February 1991). "The familial hyperchylomicronemia syndrome. New insights into underlying genetic defects". JAMA. 265 (7): 904–8. doi:10.1001/jama.1991.03460070086049. PMID 1992190.
  5. ^ Online Mendelian Inheritance in Man (OMIM): HYPERLIPOPROTEINEMIA, TYPE I - 238600, updated 03/18/2004. As of October 2012, mention of type Ia no longer appears in the OMIM record.
  6. ^ "Familial lipoprotein lipase deficiency: MedlinePlus Medical Encyclopedia". medlineplus.gov. Retrieved 17 April 2019.
  7. ^ Burnett, John R.; Hooper, Amanda J.; Hegele, Robert A. (June 22, 2017). "Familial Lipoprotein Lipase Deficiency". In Adam, MP; Ardinger, HH; Pagon, RA; et al. (eds.). GeneReviews. Seattle: University of Washington. PMID 20301485.
  8. ^ "Tryngolza (olezarsen) approved in U.S. as first-ever treatment for adults living with familial chylomicronemia syndrome as an adjunct to diet" (Press release). Ionis Pharmaceuticals. 19 December 2024. Retrieved 20 December 2024 – via PR Newswire.
  9. ^ Regalado, Antonio (May 4, 2016). "The World's Most Expensive Medicine Is a Bust". MIT Technology Review.
  10. ^ Crowe, Kelly (17 November 2018). "The million-dollar drug". CBCNews. CBC (Canadian Broadcasting Corporation). Retrieved 17 November 2018.
  11. ^ A.D.A.M. Editorial Board (2011-05-29). Dugdale, III, David C.; Zieve, David (eds.). Familial lipoprotein lipase deficiency. National Center for Biotechnology Information (published May 29, 2011). Retrieved October 15, 2012. {{cite book}}: |work= ignored (help)

Further reading

[edit]
[edit]
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