Post menopausal osteoporosis
Submitted by:Amit Kochhar B.O.T. 2nd year Pt. D.D.U. I.P.H.
Osteoporosis PATHOGENESIS DIAGNOSIS TREATMENT
Two components of the bone Cortical
Bone
Dense and compact Runs the length of the long bones, forming a hollow cylinder
Trabecular
bone
Has a light, honeycomb structure Trabeculae are arranged in the directions of tension and compression Occurs in the heads of the long bones Also makes up most of the bone in the vertebrae
Osteons Principal
organizing feature of compact bone
Haversian
canal – place for the nerve blood and lymphatic vessels Lamellae – collagen deposition pattern Lacunae – holes for osteocytes Canaliculi – place of communication between osteocytes
Bone cells Osteocytes
- derived from osteoprogenitor cells Osteoblasts Osteoclasts
Osteocytes Trapped
osteoblasts
In lacunae
Keep
bone matrix in good condition and can release calcium ions from bone matrix when calcium demands increase
Osteocytic osteolysis
Osteoblasts Make
collagen Activate nucleation of hydroxyapatite crystallization onto the collagen matrix, forming new bone As they become enveloped by the collagenous matrix they produce, they transform into osteocytes Stimulate osteoclast resorptive activity
Osteoclasts Resorbe
bone matrix from sites where it is deteriorating or not needed Digest bone matrix components Focal decalcification and extracellular digestion by acid hydrolases and uptake of digested material Disappear after resorption Assist with mineral homeostasis
Chemistry of the bone Matrix Mineral
Matrix - osteoid Collagen
type I and IV Layers of various orientations (add to the strength of the matrix) Other proteins 10% of the bone protein
Direct formation of fibers Enhance mineralization Provide signals for remodeling
Mineral A
calcium phosphate/carbonate compound resembling the mineral hydroxyapatite Ca10(PO4)6(OH)2 Hydroxyapatite crystals
Imperfect Contain Mg, Na, K
Mineralization of the bone Calcification
occurs by extracellular deposition of hydroxyapatite crystals Trapping
of calcium and phosphate ions in concentrations that would initiate deposition of calcium phosphate in the solid phase, followed by its conversion to crystalline hydroxyapatite
Mechanisms
exist to both initiate and inhibit calcification
Bone remodeling process Proceeds
in cycles – first resorption than bone formation The calcium content of bone turns over with a half-life of 1-5 years
Bone remodeling process
Coordination of Resorption and Formation Phase
I
Signal
from osteoblasts Stimulation of osteoblastic precursor cells to become osteoclasts Process takes 10 days
Coordination of Resorption and Formation Phase
II
Osteoclast
resorb bone creating cavity Macrophages clean up
Phase
III
New bone laid down by osteoblasts Takes 3 months
Pathways of differentiation of osteoclasts and osteoblasts
Hormonal Influence Vitamin
D Parathyroid Hormone Calcitonin Estrogen Androgen
Vitamin D Osteoblast
have receptors for (1,25-(OH)2-D) Increases activity of both osteoblasts and osteoclasts Increases osteocytic osteolysis (remodeling) Increases mineralization through increased intestinal calcium absorption Feedback action of (1,25-(OH)2-D) represses gene for PTH synthesis
Parathyroid Hormone
Accelerates removal of calcium from bone to increase Ca levels in blood PTH receptors present on both osteoblasts and osteoclasts Osteoblasts respond to PTH by
Change of shape and cytoskeletal arrangement Inhibition of collagen synthesis Stimulation of IL-6, macrophage colony-stimulating factor secretion
Chronic stimulation of the PTH causes hypocalcemia and leads to resorptive effects of PTH on bone
Calcitonin C
cells of thyroid gland secrete calcitonin Straight chain peptide - 32 aa Synthesized from a large preprohormone Rise in plasma calcium is major stimulus of calcitonin secretion Plasma concentration is 10-20 pg/ml and half life is 5 min
Actions of Calcitonin Osteoclasts
are target cells for calcitonin Major effect of clacitonin is rapid fall of plasma calcium concentration caused by inhibition of bone resorption Magnitude of decrease is proportional to the baseline rate of bone turnover
Other systemic hormones Estrogens Increase
bone remodeling
Androgens Increase
bone formation
Other systemic hormones Growth
hormone
Increases
bone remodeling
Glucocorticoids Inhibit
Thyroid
bone formation
hormones
Increase
bone resorption Increase bone formation
Local regulators of bone remodeling Cytokines IL-6 IL-1
Prostaglandins Growth
factors
IGF-I TGF-β
Osteoporosis A disease characterized by: low
bone mass microarchitectural deterioration of the bone tissue
Leading to: enhanced
bone fragility increase in fracture risk
WHO guidelines for determining osteoporosis Normal:
Not less than 1 SD below the avg. for young adults Osteopenia: -1 to -2.5 SD below the mean Osteoporosis: More than 2.5 SD below the young adult average
70% of women over 80 with no estrogen replacement therapy qualify
Severe
osteoporosis
More than 2.5 SD below with fractures
Osteoporosis - epidemiology Disorder
of postmenopausal women of northern European descent Increase in the incidence related to decreasing physical activity Over 27 million or 1of 3 women are affected with osteoporosis Over 5 million or 1of 5 men are affected with osteoporosis
Bone Mass
Statistics
Prevalence of Osteopenia and Osteoporosis in Postmenopausal Women by Ethnicity
Pathogenesis of Estrogen Deficiency and Bone Loss Estrogen
loss triggers increases in IL1, IL-6, and TNF due to: Reduced
suppression of gene transcription of IL-6 and TNF Increased number of monocytes Increased cytokines lead to increased osteoclast development and lifespan
Osteoclast Differentiation and Activation in Estrogen Deficiency
Impact of Estrogen on Osteoclastic Differentiation and Activation
National Osteoporosis Risk Assessment (NORA): Factors Associated With Increased Risk of Osteoporosis
NORA: Factors Associated With Reduced Risk of Osteoporosis
NORA: BMD and Fracture Rate
Osteoporosis Mechanisms Imbalance
causing osteoporosis
between rate of resorption and
formation Failure to complete 3 stages of remodeling Types Type
of osteoporosis
I Type II Secondary
Osteoporosis - types Postmenopausal
osteoporosis (type I)
Caused
by lack of estrogen Causes PTH to over stimulate osteoclasts Excessive loss of trabecular bone Age-associated Bone
osteoporosis (type II)
loss due to increased bone turnover Malabsorption Mineral and vitamin deficiency
Secondary osteoporosis
Osteoporotic vertebra
Normal vs. osteoporotic bone
Risk Factors
When to Measure BMD in Postmenopausal Women All
women 65 years and older Postmenopausal women <65 years of age: If
result might influence decisions about intervention One or more risk factors History of fracture
When Measurement of BMD Is Not Appropriate Healthy
premenopausal women Healthy children and adolescents Women initiating ET/HT for menopausal symptom relief (other osteoporosis therapies should not be initiated without BMD measurement)
Prediction of Fracture Risk All
techniques (DXA, QCT, QUS) predict fracture risk
Osteoporosis can be Assessed by DXA
s ite
ll S A
V
er te br
al
Forearm Hip Spine
H ip
re ar m
3 2.5 2 1.5 1 0.5 0 Fo
Relative Risk
Relative Risk of Fracture per SD Decrease in BMD
DXA-assessed content is a proven effective method for assessing osteoporosis related fracture risk. Population surveys and research studies demonstrate a decrease in bone density measured by DXA predicts fracture at specific sites. Marshall, D, et al: Meta-analysis of how well measures of bone mineral density predict occurrence of osteoporotic fractures. British Medical Journal. 312:1254-1259, 1996.
The McCue CUBA: Ultrasonometry Technology that can Assess Osteoporosis
BUA
110 Normal dB/MHz
40 dB/MHz Osteoporotic Bone Frequency
Heel BUA is Significantly Lower in Subjects With Future Hip Fracture. 60
BUA (dB/sq MHz)
50 40 30 20 10 0 Fracture
No Fracture
Subjects who developed hip fracture showed significantly (p<0.001) lower heel BUA results in a two-year follow-up prospective study of 1,414 subjects. Porter, RW, et al: Prediction of hip fracture in elderly women: a prospective study. British Medical Journal. 301:638-641, 1990.
Discriminating Power of Heel BUA in Reflecting Vertebral Osteoporosis When assessing vertebral osteoporosis, there was no statistically significant difference in the discriminating power of Heel BUA or Spine, Femur Neck or Trochanter BMD by DXA. Ohishi, T, et al: Ultrasound measurement using CUBA clinical system can discriminate between women with and without vertebral fracture. Journal of Clinical Densitometry. 3:227-231, 2000. 1
Area Under the Curve
0.9 0.8 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0 Heel BUA
Spine BMD
Neck BMD
Trochanter BMD
Receiver Operator Characteristic Analysis of Hip Fracture Risk 0.9
Area Under the Curve
0.85 0.8 0.75 0.7 0.65 0.6 0.55 0.5 Heel BUA
Fem ur Neck BMD
Schott, AM, et al: Ultrasound discriminates patients with hip fracture equally well as dual energy x-ray absorptiometry and independently of bone mineral density. Journal of Bone and Mineral Research. 10:243-249, 1995.
Increasing Relative Fracture Risk is Seen with Decreased BUA or BMD Hans, D, et al: Ultrasonographic heel measurements to predict hip fracture in elderly women: the EPIDOS prospective study. Lancet. 348:511-514, 1996. Bauer, DC, et al: Broadband ultrasound attenuation predicts fractures strongly and independently of densitometry in older women. Archieves of Internal Medicine. 157:629-634, 1997. Frost, ML, et al: A comparison of fracture discrimination using calcaneal quantitative ultrasound and dual x-ray absorptiometry in women with a history of fracture at sites other than the spine and hip. Calcified Tissue International. 71:207-211, 2002. Relative Risk of Fracture
3 2.5 2 BUA
1.5
BMD
1 0.5 0 Hans, et al
Bauer, et al Research Study
Frost, et al
Increased Relative Fracture Risk is Seen With Decreasing BUA 14,824 men and women were followed for an average of 1.9 years to relate BUA to future fracture risk. Subjects in the lowest 10th percentile of BUA showed a relative risk of fracture 4.44 times greater than those in the highest 30th percentile of BUA.
Relative Fracture Risk
Khaw, KT, et al. Prediction of total and hip fracture risk in men and women by quantitative ultrasound of the calcaneus: EPIC-Norfolk prospective study. Lancet. 363:197-202, 2004. 5 4.5 4 3.5 3 2.5 2 1.5 1 0.5 0 <10
10 to <40
40 to <70
Percentile Category
70 to 100
Who Should Be Considered for Prevention or Treatment? Postmenopausal
women with T-score below –2.0 with no risk factors Postmenopausal women with T-score below –1.5 with one or more risk factors
NORA
NORA
Prevention of Bone Loss Prevention of Bone Loss Calcium HRT SERMS Calcitonin Bisphosphonates
Calcium Supplementation
HOPE Trial
PEPI Trial
BMD
Spine BMD
Total Hip BMD
Forearm BMD
WHI Results
WHI Results
Summary