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Pregnancy in homozygous familial hypercholesterolemia--Importance of LDL-apheresis
M. Blaha, M. Lanska, V. Blaha, L. Boudys, P. Zak,
Jazyk angličtina Země Nizozemsko
Typ dokumentu kazuistiky, časopisecké články, práce podpořená grantem
Grantová podpora
NT14265
MZ0
CEP - Centrální evidence projektů
NT14037
MZ0
CEP - Centrální evidence projektů
- MeSH
- biologické markery krev MeSH
- časové faktory MeSH
- fenotyp MeSH
- genetická predispozice k nemoci MeSH
- homozygot * MeSH
- hyperlipoproteinemie typ II krev diagnóza genetika terapie MeSH
- imunosorpční techniky * MeSH
- komplikace těhotenství krev diagnóza genetika terapie MeSH
- LDL-cholesterol krev MeSH
- LDL-receptory genetika MeSH
- lidé MeSH
- mutace * MeSH
- mutační analýza DNA MeSH
- narození živého dítěte MeSH
- separace krevních složek metody MeSH
- stupeň závažnosti nemoci MeSH
- těhotenství MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- práce podpořená grantem MeSH
INTRODUCTION: Rare cases of pregnancy in women with homozygous familial hypercholesterolemia (HFH) have been reported. HFH might pose significant risks for the mother and her fetus. Statins, the most potent agents for low-density lipoprotein (LDL) cholesterol reduction, are contraindicated; thus lipoprotein apheresis remains the only effective treatment. CASE REPORT: We report on a 34-year-old pregnant woman with HFH who was treated throughout the entire pregnancy by lipoprotein apheresis (immunoadsorption method). Increasing levels of LDL-cholesterol were stabilized at 9-10 mmol/L by lipoprotein apheresis (performed every 10 days). No complications were observed during the treatment procedures. Monitoring of the fetus revealed no impairment of the umbilical cord and blood flow in the uterine arteries, as well as no intrauterine growth retardation. The delivery was spontaneous and the child was breastfed for two months. CONCLUSION: Intensive treatment by lipoprotein apheresis is an effective and safe therapeutic strategy during pregnancy, even in severe cases of HFH, as it can stabilize progressively increasing lipoprotein levels and prevent severe complications.
Citace poskytuje Crossref.org
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- $a INTRODUCTION: Rare cases of pregnancy in women with homozygous familial hypercholesterolemia (HFH) have been reported. HFH might pose significant risks for the mother and her fetus. Statins, the most potent agents for low-density lipoprotein (LDL) cholesterol reduction, are contraindicated; thus lipoprotein apheresis remains the only effective treatment. CASE REPORT: We report on a 34-year-old pregnant woman with HFH who was treated throughout the entire pregnancy by lipoprotein apheresis (immunoadsorption method). Increasing levels of LDL-cholesterol were stabilized at 9-10 mmol/L by lipoprotein apheresis (performed every 10 days). No complications were observed during the treatment procedures. Monitoring of the fetus revealed no impairment of the umbilical cord and blood flow in the uterine arteries, as well as no intrauterine growth retardation. The delivery was spontaneous and the child was breastfed for two months. CONCLUSION: Intensive treatment by lipoprotein apheresis is an effective and safe therapeutic strategy during pregnancy, even in severe cases of HFH, as it can stabilize progressively increasing lipoprotein levels and prevent severe complications.
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