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Prognostic and functional importance of both overt and subclinical left ventricular systolic dysfunction in systemic sclerosis.
Fairley, Jessica L; Hansen, Dylan; Proudman, Susanna; Sahhar, Joanne; Ngian, Gene-Siew; Walker, Jenny; Host, Lauren V; La Gerche, André; Prior, David; Burns, Andrew; Morrisroe, Kathleen; Stevens, Wendy; Nikpour, Mandana; Ross, Laura.
Affiliation
  • Fairley JL; Department of Medicine, The University of Melbourne, Melbourne, Victoria, Australia; Department of Rheumatology, St. Vincent's Hospital Melbourne, Melbourne, Victoria, Australia. Electronic address: jessica.fairley@svha.org.au.
  • Hansen D; Department of Rheumatology, St. Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
  • Proudman S; Department of Medicine, The University of Adelaide, Adelaide, South Australia, Australia; Department of Rheumatology, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
  • Sahhar J; Department of Rheumatology, Monash Health, Melbourne, Victoria, Australia; Department of Medicine, Monash University, Melbourne, Victoria, Australia.
  • Ngian GS; Department of Rheumatology, Monash Health, Melbourne, Victoria, Australia; Department of Medicine, Monash University, Melbourne, Victoria, Australia.
  • Walker J; Department of Rheumatology, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
  • Host LV; Fiona Stanley Hospital, Perth, Western Australia, Australia.
  • La Gerche A; Department of Medicine, The University of Melbourne, Melbourne, Victoria, Australia; Department of Cardiology, St. Vincent's Hospital Melbourne, Melbourne, Victoria, Australia; The Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
  • Prior D; Department of Cardiology, St. Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
  • Burns A; Department of Cardiology, St. Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
  • Morrisroe K; Department of Medicine, The University of Melbourne, Melbourne, Victoria, Australia; Department of Rheumatology, St. Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
  • Stevens W; Department of Rheumatology, St. Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
  • Nikpour M; Department of Medicine, The University of Melbourne, Melbourne, Victoria, Australia; Department of Rheumatology, St. Vincent's Hospital Melbourne, Melbourne, Victoria, Australia; The University of Sydney School of Public Health, Sydney, New South Wales, Australia; Royal Prince Alfred Hospital Sydney
  • Ross L; Department of Medicine, The University of Melbourne, Melbourne, Victoria, Australia; Department of Rheumatology, St. Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
Semin Arthritis Rheum ; 66: 152443, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38631275
ABSTRACT

OBJECTIVES:

To quantify the frequency and clinical implications of systemic sclerosis (SSc)-associated left ventricular function (LV) impairment.

METHODS:

Australian Scleroderma Cohort Study participants meeting ACR/EULAR criteria for SSc with ≥1 echocardiographic LVEF measurement were included. Overt LV dysfunction was indicated by reduced LV ejection fraction (LVEF) and subclinical LV dysfunction was measured using impaired LV global longitudinal strain (LV-GLS>-16 %). Those with secondary causes of LV dysfunction (myocardial ischaemia, valvulopathy and pulmonary arterial hypertension) were excluded. Chi-squared tests, two-sample t-tests or Wilcoxon rank-sum tests were used for between-group comparison as appropriate. Generalised estimating equations(GEE) were used to model longitudinal data. Kaplan-Meier and Cox proportional hazard models were used for survival analyses.

RESULTS:

Of 1141 participants with no co-morbid cardiac disease, 2.4 % ever recorded a LVEF<50 %, while only 0.6 % ever recorded a LVEF≤40 %. LV-GLS data were available for 90 % of participants at one centre (n = 218). Impaired LV-GLS was detected in 21 % despite LVEF≥50 %. Those with a LVEF<50 % were more frequently male (p = 0.01) with dcSSc (p < 0.01), higher inflammatory markers (p < 0.02) and skeletal muscle disease (p < 0.05). In multivariable analyses, recording a LVEF<50 % was associated with increased mortality (HR2.3, 95 %CI1.0-4.8, p = 0.04). Impaired LV-GLS was also associated with poorer survival in univariable analyses (HR3.4, 95 %CI1.0-11.8, p = 0.05). Those with a LVEF<50 % more frequently recorded WHO Class III/IV dyspnoea (OR3.5, 95 %CI1.6-7.7, p < 0.01), with shorter six-minute walk distance (p = 0.01), higher Health Assessment Questionnaire-Disability Index scores (p < 0.01) and lower Short Form-36 Physical Component Summary scores (p = 0.02). Increased dyspnoea (WHO Class III/IV dyspnoea; OR3.6, 95 %CI1.4-9.2, p < 0.01) was also seen in those with impaired LV-GLS.

CONCLUSIONS:

Both overt and subclinical SSc-associated LV dysfunction are associated with worse survival and impaired physical function. The frequency of abnormal LV-GLS in those with consistently normal LVEF suggests an under-appreciated burden of subtle LV systolic dysfunction in SSc that has a significant impact on patient symptomatology.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Health context: 6_ODS3_enfermedades_notrasmisibles Database: MEDLINE Main subject: Scleroderma, Systemic / Ventricular Dysfunction, Left Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: Semin Arthritis Rheum Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Health context: 6_ODS3_enfermedades_notrasmisibles Database: MEDLINE Main subject: Scleroderma, Systemic / Ventricular Dysfunction, Left Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: Semin Arthritis Rheum Year: 2024 Document type: Article