A patient with homozygous familial hypercholesterolemia who was receiving LDL apheresis suffered an acute myocardial infarction after PCSK9 inhibitor treatment was started

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  • PCSK9阻害薬の開始後急性心筋梗塞を発症したLDLアフェレーシス施行中の家族性高コレステロール血症ホモ接合体の1例
  • 症例報告 PCSK9阻害薬の開始後急性心筋梗塞を発症したLDLアフェレーシス施行中の家族性高コレステロール血症ホモ接合体の1例
  • ショウレイ ホウコク PCSK9 ソガイヤク ノ カイシ ゴ キュウセイ シンキン コウソク オ ハッショウ シタ LDL アフェレーシス シコウ チュウ ノ カゾクセイ コウコレステロール ケッショウ ホモ セツゴウタイ ノ 1レイ

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Abstract

<p>A 66-year-old male patient was diagnosed with homozygous familial hypercholesterolemia (FH) 29 years ago and had been receiving low-density lipoprotein (LDL) apheresis twice a month. He underwent coronary artery bypass grafting for unstable angina pectoris. His serum LDL-cholesterol (LDL-C) level before LDL apheresis was 126 mg/dL while he was receiving atorvastatin and ezetimibe. As an FH patient with cardiovascular disease, his serum LDL-C level was a little high compared with the target level of 70 mg/dL. He started to receive a PCSK9 inhibitor in addition to the standard therapy to lower his LDL-C level, and the frequency of LDL apheresis was reduced from twice to once a month, because puncturing became difficult and imposed a large burden on the patient. The patient suffered a myocardial infarction five months after the PCSK9 inhibitor treatment was started, even though his serum LDL-C level had fallen (62.7 mg/dL before and 21.3 mg/dL after LDL apheresis). His cardiac function improved after a percutaneous coronary intervention targeting the right coronary artery.</p>

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