Anti PCSK9 Monoclonal Antibody Treatment in Elderly Patients: A Real-world Clinical Experience.


Journal

The Israel Medical Association journal : IMAJ
ISSN: 1565-1088
Titre abrégé: Isr Med Assoc J
Pays: Israel
ID NLM: 100930740

Informations de publication

Date de publication:
Feb 2024
Historique:
medline: 29 2 2024
pubmed: 29 2 2024
entrez: 29 2 2024
Statut: ppublish

Résumé

The use of proprotein convertase subtilisin/kexin type 9 monoclonal antibodies (PCSK9 mAbs) is emerging for lowering low-density lipoprotein cholesterol (LDL-C). However, real-world data is lacking for their use among elderly patients. To define the characteristics of elderly patients treated with PCSK9 mAbs and to evaluate the efficacy and tolerability compared with younger patients. We conducted a retrospective cohort study of elderly patients (≥ 75 years at enrollment) treated with PCSK9 mAbs for primary and secondary cardiovascular prevention. Data were retrieved for demographic and clinical characteristics; indications for treatment; agents and dosages; concomitant lipid lowering treatment; LDL-C levels at baseline, 6, 12 months, and at the end of follow up. Data also included achieving LDL-C target levels and adverse effects. The cohort included 91 elderly patients and 92 younger patients, mean age 75.2 ± 3.76 and 58.9 ± 7.4 years (P < 0.0001). Most patients (82%, 80%) were in high/very high-risk categories. For almost all (98%, 99%), the indication was statin intolerance, with PCSK9 mAb monotherapy the most prevalent regimen. The average follow-up was 38.1 ± 20.5 and 30.9 ± 15.8 months (P = 0.0258). Within 6 months the LDL-C levels were reduced by 57% in the elderly group and by 59% in the control group (P = 0.2371). Only 53% and 57% reached their LDL-C target levels. No clinically significant side effects were documented. PCSK9 mAbs have similar effects and are well tolerated among elderly patients as in younger patients.

Sections du résumé

BACKGROUND BACKGROUND
The use of proprotein convertase subtilisin/kexin type 9 monoclonal antibodies (PCSK9 mAbs) is emerging for lowering low-density lipoprotein cholesterol (LDL-C). However, real-world data is lacking for their use among elderly patients.
OBJECTIVES OBJECTIVE
To define the characteristics of elderly patients treated with PCSK9 mAbs and to evaluate the efficacy and tolerability compared with younger patients.
METHODS METHODS
We conducted a retrospective cohort study of elderly patients (≥ 75 years at enrollment) treated with PCSK9 mAbs for primary and secondary cardiovascular prevention. Data were retrieved for demographic and clinical characteristics; indications for treatment; agents and dosages; concomitant lipid lowering treatment; LDL-C levels at baseline, 6, 12 months, and at the end of follow up. Data also included achieving LDL-C target levels and adverse effects.
RESULTS RESULTS
The cohort included 91 elderly patients and 92 younger patients, mean age 75.2 ± 3.76 and 58.9 ± 7.4 years (P < 0.0001). Most patients (82%, 80%) were in high/very high-risk categories. For almost all (98%, 99%), the indication was statin intolerance, with PCSK9 mAb monotherapy the most prevalent regimen. The average follow-up was 38.1 ± 20.5 and 30.9 ± 15.8 months (P = 0.0258). Within 6 months the LDL-C levels were reduced by 57% in the elderly group and by 59% in the control group (P = 0.2371). Only 53% and 57% reached their LDL-C target levels. No clinically significant side effects were documented.
CONCLUSIONS CONCLUSIONS
PCSK9 mAbs have similar effects and are well tolerated among elderly patients as in younger patients.

Identifiants

pubmed: 38420988

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

130-135

Auteurs

Ela Giladi (E)

Department of Cardiology, Meir Medical Center, Kfar Saba, Israel.

Roy Israel (R)

Department of Internal Medicine C, Meir Medical Center, Kfar Saba, Israel.

Wasseem Daud (W)

Department of Internal Medicine C, Meir Medical Center, Kfar Saba, Israel.

Chen Gurevitz (C)

Department of Cardiology, Meir Medical Center, Kfar Saba, Israel, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Alaa Atamna (A)

Infectious Diseases, Rabin Medical Center (Beilinson Campus), Petah Tikva, Israel, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

David Pereg (D)

Department of Cardiology, Meir Medical Center, Kfar Saba, Israel, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Abid Assali (A)

Department of Cardiology, Meir Medical Center, Kfar Saba, Israel, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Avishay Elis (A)

Department of Internal Medicine C, Meir Medical Center, Kfar Saba, Israel, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Classifications MeSH