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January 1, 2016Internal Medicine25 citationsOpen Access

Is There an Increased Arterial Stiffness in Patients with Primary Sjgren's Syndrome?

MDMeltem Seziş DemirciGKGonca KarabulutÖGÖzkan Güngör

Key Result

Primary Sjögren's syndrome was associated with significantly increased arterial stiffness compared to healthy controls, evidenced by a higher mean carotid-femoral pulse wave velocity (8.2 vs. 7.5 m/s).

Study Design

Type

Case-Control (n=143)

Multicenter

No

Structured PICO

Does primary Sjögren's syndrome increase arterial stiffness in female patients compared to healthy controls?

P
Population
143 female participants, including 75 with primary Sjögren's syndrome free of pre-existing cardiovascular disease and 68 matched healthy controls, assessed for arterial stiffness.
E
Exposure
Primary Sjögren's syndrome (disease exposure)
C
Comparator
68 age-, sex- and body mass index-matched healthy control subjects
O
Outcome
Arterial stiffness assessed by measurement of the carotid-femoral pulse wave velocity (PWV)surrogate

Female patients with primary Sjögren's syndrome exhibit significantly increased arterial stiffness compared to healthy controls, suggesting a higher risk of subclinical atherosclerosis.

Main Result

Absolute Event Rate: 8.2% vs 7.5%

p-value: p=0.01

Limitations

  • A high proportion of patients were taking medications such as steroids, antihypertensive drugs, and statins, which could not be stopped or excluded.
  • Cannot exclude the possibility that higher PWV in pSS patients is caused by the use of steroids, hypertension, and dyslipidemia rather than the disease itself.
  • High proportion of patients taking medications such as steroids, antihypertensive drugs, and statins that could not be stopped
  • Cannot exclude the possibility that higher PWV in pSS patients is caused by the use of steroids, hypertension, and dyslipidemia rather than pSS itself

Abstract

OBJECTIVE: Primary Sjögren's syndrome (pSS) is a common chronic autoimmune disease that primarily affects the salivary and lacrimal glands. Arterial stiffness is one of the earliest detectable manifestations of adverse structural and functional changes within the vessel wall. The aim of this study was to evaluate the relationship between arterial stiffness and pSS. METHODS: In this study, 75 female patients with pSS who fulfilled the American European Consensus Criteria for Sjögren's syndrome, were included. A total of 68 age-, sex- and body mass index-matched subjects were recruited as the control population. Arterial stiffness was assessed by measurement of the carotid-femoral pulse wave velocity (PWV). RESULTS: The mean age of the patients was 54.0±9.3 years and the median duration of the disease was 10 years. Compared with the control subjects, patients with pSS had a higher mean PWV (8.2±1.5 m/s vs. 7.5±1.4 m/s; p=0.01). Correlation analysis showed that the PWV was positively correlated with age, body mass index, serum cholesterol, low-density lipoprotein (LDL) and C-reactive protein levels, blood pressure, mean arterial pressure (MAP), pulse pressure and left ventricular mass index. A multiple linear regression analysis revealed that arterial stiffness was associated with age, MAP and LDL levels in pSS patients. CONCLUSION: Although patients with pSS appear to have increased arterial stiffness, risk factors associated with arterial stiffness in these patients are similar to the general population. However, we cannot exclude the possibility that a higher PWV in pSS patients is caused, not by pSS itself, but by the use of steroids, hypertension and dyslipidemia.

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Cite This Study

Demirci et al. (2016) conducted a case-control in Primary Sjögren's Syndrome (n=143). Primary Sjögren's Syndrome vs. Healthy controls was evaluated on Arterial stiffness assessed by carotid-femoral pulse wave velocity (PWV) (p=0.01). Primary Sjögren's syndrome was associated with significantly increased arterial stiffness compared to healthy controls, evidenced by a higher mean carotid-femoral pulse wave velocity (8.2 vs. 7.5 m/s).

synapsesocial.com/papers/6a707cc65d37378ac1dd97ddhttps://doi.org/10.2169/internalmedicine.55.3472
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